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Archive for the ‘Genetic Engineering’ Category

Genetic Engineering – an overview | ScienceDirect Topics

Saturday, July 11th, 2020

2.08.1 Introduction to Genetic Engineering

With the discovery of DNA as the universal genetic material in 1944 [1] and the elucidation of its molecular structure approximately a decade later [2], the era of DNA science and technology had officially begun. However, it wasnt until the 1970s that researchers began manipulating DNA with the use of highly specific enzymes, such as restriction endonucleases and DNA ligases. The experiments in molecular biology conducted within Stanford University and the surrounding Bay Area in 1972 represent the earliest examples of recombinant DNA technology and genetic engineering [3, 4]. Specifically, a team of molecular biologists were able to artificially construct a bacterial plasmid DNA molecule by splicing and combining fragments from two naturally occurring plasmids of distinct origin. The resulting recombinant DNA was then introduced into a bacterial Escherichia coli host strain for replication and expression of the resident genes. This famous example represents the first use of recombinant DNA technology to generate a genetically modified organism.

In general, genetic engineering (Figure 1) refers to all the techniques used to artificially modify an organism in order to produce a desired substance (such as an enzyme or a metabolite) that is not naturally produced by the organism, or to enhance a preexisting cellular process. As a first step, the desired DNA segment or gene is isolated from a source organism by extracting and purifying the total cellular DNA. The DNA is then manipulated using numerous laboratory techniques and inserted into a genetic carrier molecule in order to be delivered to the host strain. The means of gene delivery is dependent upon the type of organism involved and can be classified into viral and nonviral methods. Transformation (nonviral, for bacteria and lower eukaryotes), transfection (viral and nonviral, for eukaryotes), transduction (viral, for bacteria), and conjugation (cell-to-cell, for bacteria) are all commonly used methods for gene delivery and DNA transfer. Because no method of gene delivery is capable of transforming every cell within a population, the ability to distinguish recombinant cells from nonrecombinants constitutes a crucial aspect of genetic engineering. This step frequently involves the use of observable phenotypic differences between recombinant and nonrecombinant cells. In rare instances where no selection of recombinants is available, laborious screening techniques are required to locate an extremely small subpopulation of recombinant cells within a substantially larger population of wild-type cells.

Figure 1. Basic genetic engineering process scheme including replication and expression of recombinant DNA according to the central dogma of molecular biology.

Although cells are composed of various biomolecules including carbohydrates, lipids, nucleic acids, and proteins, DNA is the primary manipulation target for genetic engineering. According to the central dogma of molecular biology, DNA serves as a template for replication and gene expression, and therefore harnesses the genetic instructions required for the functioning of all living organisms. Through gene expression, coding segments of DNA are transcribed to form messenger RNAs, which are subsequently translated to form polypeptides or protein chains. Therefore, by manipulating DNA, we can potentially modify the structure, function, or activity of proteins and enzymes, which are the final products of gene expression. This concept forms the basis of many genetic engineering techniques such as recombinant protein production and protein engineering. Furthermore, virtually every cellular process is carried out and regulated by enzymes, including the reactions, pathways, and networks that constitute an organisms metabolism. Therefore, a cells metabolism can be deliberately altered modifying or even restructuring native metabolic pathways to lead to novel metabolic activities and capabilities, an application known as metabolic engineering. Such metabolic engineering approaches are often realized through DNA manipulation.

The first genetically engineered product approved by the US Food and Drug Administration (FDA) for commercial manufacturing appeared in 1982 when a strain of E. coli was engineered to produce recombinant human insulin [5]. Prior to this milestone, insulin was obtained predominantly from slaughterhouse animals, typically porcine and bovine, or by extraction from human cadavers. Insulin has a relatively simple structure composed of two small polypeptide chains joined through two intermolecular disulfide bonds. Unfortunately, wild-type E. coli is incapable of performing many posttranslational protein modifications, including the disulfide linkages required to form active insulin. In order to overcome this limitation, early forms of synthetic insulin were manufactured by first producing the recombinant polypeptide chains in different strains of bacteria and linking them through a chemical oxidation reaction [5]. However, nearly all current forms of insulin are produced using yeast rather than bacteria due to the yeasts ability to secrete a nearly perfect replica of human insulin without requiring any chemical modifications. Following the success of recombinant human insulin, recombinant forms of other biopharmaceuticals began appearing on the market, such as human growth hormone in 1985 [6] and tissue plasminogen activator in 1987 [7], all of which are produced using the same genetic engineering concepts as applied to the production of recombinant insulin.

As a result of the sheer number of applications and immense potential associated with genetic engineering, exercising bioethics becomes necessary. Concerns pertaining to the unethical and unsafe use of genetic engineering quickly arose with the advent of gene cloning and recombinant DNA technology in the 1970s, predominantly owing to a general lack of understanding and experience regarding the new technology. The ability of scientists to interfere with nature and alter the genetic makeup of living organisms was the focal point of many concerns surrounding genetic engineering. Although it is widely assumed that the potential agricultural, medical, and industrial benefits afforded by genetic engineering greatly outweigh the inherent risks surrounding such a powerful technology, most of the moral and ethical concerns raised during the inception of genetic engineering are still actively expressed today. For this reason, all genetically modified products produced worldwide are subject to government inspection and approval prior to their commercialization. Regardless of the application in question, a great deal of responsibility and care must be exercised when working with genetically engineered organisms to ensure the safe handling, treatment, and disposal of all genetically modified products and organisms.

As the field of biotechnology relies heavily upon the application of genetic engineering, this article introduces both the fundamental and applied concepts with regard to current genetic engineering methods and techniques. Particular emphasis shall be placed upon the genetic modification of bacterial systems, especially those involving the most famous workhorse E. coli on account of its well-known genetics, rapid growth, and ease of manipulation.

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Genetic Engineering: Pros & Cons – E&C

Saturday, July 11th, 2020

I think the ethics and morals of genetic engineering are very complicated. It intrigues me.

Roger Spottiswoode

Genetic engineering can be defined as manipulation of an organisms genes with the help of biotechnology.

The first official genetic manipulation happened in 1972 by Paul Berg when he combined the DNA from a monkey virus with the lambda virus.

Genetic engineering is a very controversial topic in our society. There are many pros and cons regarding this topic.

In the following, the advantages as wells as the downsides of genetic manipulation are examined.

In order to create a genetically modified organism, scientists first have to choose what gene they want to insert into the organism. With the help of genetic screens, potential genes can be tested with the goal of finding the best candidates.

When a suitable gene has been determined, the next step is to isolate it. The cell which contains the gene has to be opened and the DNA has to be purified.

After isolating the gene, it is ligated into a plasmid which is inserted into a bacterium. Thus, whenever the bacterium divides, the plasmid is also replicated. This leads to a vast number of copies of this gene.

Before inserting the gene into the target organism, it has to be combined with other genetic elements including a terminator and promoter region which end and initiate the transcription.

In the final step, the genetic material is inserted into a host genome. After that, the genetic engineering process is finished.

Genetic engineering is often used by scientists to improve their understanding on how genetics actually work and how they affect our talents and our decisions.

From these findings, scientists can provide insights for medical purposes and thus increase the probability for curing serious diseases in the future.

There are many important areas in the field of medicine in which genetic manipulation could contribute to a better treatment of diseases. This also includes the invention of more effective drugs with less side effects.

Moreover, model animals can be genetically modified in hope to get new insights on how these modifications would work on humans.

For this purpose, using mice in order to examine the effects of genetic manipulation on obesity, cancer, heart diseases and other serious conditions is common practice in nowadays scientific work.

Genetic engineering is also used in the field of agriculture in order to increase yields and also make plants more resistant to pests. Moreover, even genetic experiments on livestock have been performed in the past.

Apart from the use for consumption, plants have also been genetically modified for medical purposes. By changing the gene structure of plants, scientists want to examine if they could produce new drugs which can cure diseases more effectively.

Genetic manipulation is also a field of interest for industrial purposes. Since through genetic engineering processes, all kinds of properties of animals and plants can be modified, this also comes down to a potential increase in revenue for firms if they are able to optimize the gene structure for their purposes. An example for this is the use of genetically modified bacteria for making biofuels.

The rules for genetic engineering vary significantly across different countries. However, there is some consensus on the level of danger genetic modification poses to humanity.

For example, the majority of scientists claim that there is no greater risk to human health from genetically modified crops compared to conventional food.

However, before making this genetically modified food available for public consumption, it has to be tested extensively in order to exclude any possibility of danger.

Moreover, some groups like Greenpeace or the World Wildlife Fund claim that genetically modified food should be tested more rigorously before releasing it for public consumption.

There are some severe diseases which we will likely never be able to fight if we do not use genetic engineering. From only small manipulations of genes, it is expected that we can fight a significant number of deadly diseases. Moreover, even for unborn babies, there could be genetic diseases detected.

The most prominent example for this kind of genetic disease is the Down syndrome. If our scientists get quite advanced, it is likely that we would be able to cure all genetic diseases, even that of unborn children.

Abortions because of the diagnosis of genetic diseases would no longer be necessary since we could ensure the babies health through genetic manipulation.

Since we can fight many diseases with genetic engineering, the overall life expectancy of people is likely to increase since the dangers of death due to these diseases decreases. Moreover, if we are able to further improve our knowledge regarding genetic modification, diseases could be treated more effectively.

Especially in poor countries where some diseases can cause the death of many people, also the development of genetically modified plants for medical use could be a great measure in order to mitigate the issue. We could also fight diseases which usually cause death for old people and thus prolong their lifes.

Moreover, we can increase their life quality since old people do not have to suffer from these diseases anymore. Thus, genetic engineering may lead to an increase in average life expectancy.

With the help of genetic manipulation, we could increase the variety of foods and drinks for our daily consumption. Moreover, we could further improve the crop yields since we could create sorts of plants that are resistant to all kinds of pests. Thus, we could supply enough food to all people worldwide and fight famine in an effective way.

Additionally, with the help of genetic engineering, it may be possible to create more nutritious food. This would be especially beneficial in countries where people suffer from vitamin deficiencies. If we are able to increase the level of this vitamins in crops or other foods, we could help people to overcome their vitamin deficiency.

If we are able to modify the genetics in a way that they naturally become resistant against pests, we will no longer have to use harmful chemical pesticides. Thus, genetic engineering may also lead to a reduction in the use of pesticides.

With the help of genetic engineering, we may also be able to create certain medical foods which may also replace some of the common injections. Medical foods may also help to prevent certain diseases. Therefore, genetic engineering could also lead to an improvement of medical standards.

Through genetic engineering, it would be possible to create plant species which need less water than the plant species currently used in agriculture.

By replacing the natural species with genetically modified ones, farmers could save plenty of water. This would be especially useful in regions where water shortage is a serious problem.

Water shortage will be a quite big issue in the future due to global warming. If the average temperature increases, water scarcity is likely to also increase.

Thus, with the help of genetic modification, water can be saved and the problem of water shortages may be mitigated to a certain extent.

We may also be able to increase the speed of growth of plants and animals. By doing so, we could produce more food in a given period of time. This may quite important since our world population is growing and therefore the demand for food is increasing.

Through genetic modification, we may also be able to strengthen specific characteristics of plants. This may include that plants are better able to adapt to the global warming problem or that they may become more resistant to changes in their natural conditions.

Many followers of religions are strictly against genetic engineering since they think playing god should not be a task performed by humans. There are also ethic concerns if genetic manipulation should become a valid instrument for changing the course of our lifes.

There is also the argument that diseases are a natural phenomenon and that they have a role in nature since they persisted over a quite long time horizon of evolution. Moreover, there are many scientists who believe that the creation of designer babies could not be in the interest of humanity.

If perfected, parents could choose the eye color, hair color or even the sex of the baby. This could lead to an optimization contest in our society which could also have vast negative effects if pushed too far.

Genetic manipulation can also cause genetic problems if we do not handle it in a proper way. Since science is still on an early stage on the understanding of genetics, manipulations of genes may even do more harm than good at our current state of genetic understanding. Errors could even lead to the development of new diseases or to miscarriages.

Genetic engineering also poses a risk to human health. For example, genetically modified food may lead to long-term health issues. There is just not enough reliable data yet on how harmful genetic engineering really is in the long term. Thus, it may pose serious health effects, some of them currently even unknown by scientists.

Genetic engineering may also lead to the development of allergies against certain food items. Since the DNA-structure is altered in the genetic modification process, food that has former been uncritical for people could now cause allergic reactions.

Genetic engineering is also used to modify plants. Specifically, some plant species have been developed which include their own pesticide which can protect them from animals and insects.

In this way, scientists hope to be able to increase crop yields. However, this altering of genetic code in plants can lead to a resistance of certain insects to the pesticide.

This may pose big problems to the agricultural system since if insects or other pests become resistant against toxins, they are harder to fight.

Thus, in the short run, altering genetic material in plants may have its advantages. However, in the long run, there may be severe issues when it comes to resistance of pest strains.

Some researchers are afraid that genetic engineering may also lead to a resistance against antibiotics for humans. This may lead to serious problems since the treatment of diseases with antibiotics will not be effective anymore.

Genetic engineering would also lead to a reduction in genetic diversity. Since the process of gene manipulation would be quite expensive, only rich people would be able to afford it.

Thus, this would likely lead to human behavior which favors being rich over all other things in order to be able to afford genetic manipulation. As a consequence, the variety of human behavior would be reduced.

Since genetically modified plants often contain own pesticides, they can be quite harmful to animals which are consuming these kinds of plants. Animals can suffer severe diseases from these pesticides and even die.

This problem is especially severe for butterflies and other insects which usually rely on certain plants in their near surroundings. If the natural versions of plants are replaced by genetically modified plants containing pesticides, these insects are likely to suffer from severe health conditions.

Researchers found that residues of genetically modified plants persist on the soil of fields for many months. Thus, the activity of microbes is adversely affected which can lead to a loss in fertility of the soil.

If genetically modified plants are more resistant against pests, chances are that they will displace local natural plant species in the long run. This also contributes to a reduction in genetic variety and can cause the issues related to this phenomenon.

Genetic engineering is an area which can be quite profitable for some firms. However, it is also quite expensive field of study. There are some big companies which have huge control over the seed market and thus also have a big influence on political decisions regarding the admission of genetically engineered plants for agricultural purposes.

Thus, even if there may be dangers from these admissions, companies may still get permission to sell the genetically modified seeds since they may have high influence on political decision makers.

Golden rice, unlike any other sort of rice, also contains provitamin A. It is estimated that a lack of this vitamin causes up to 500.000 cases of blindness across children each year.

Moreover, around one million people even die from a lack of this vitamin. Thus, the introduction of this gene manipulated golden rice could mitigate this problem.

Genes from the mouse-ear cress are studied extensively since they help scientists to understand the nature of a variety of plant characteristics concerning photosynthetic activity, droughts, growth speed and many more.

After finding the genes related to different characteristics of the mouse-ear cress, they can be used to modify the genes of cultivated species in order to improve their yields and resistance.

Even just a small modification in the genes of onions have led to significant effects. On the one hand, the modified onion doesnt make people cry anymore when they cut it. On the other hand, the concentration of healthy compounds like sulphur-containing substances has been increased.

There has been attempts to lower the concentration of saturated fatty acids in soy oil. Moreover, there are also companies trying to increase the level of omega-3 fatty acids of their oils.

In order to fight the osteoporosis problem, genetically modified carrots with a higher concentration of organically bound calcium have been produced. Studies have shown that humans were able to absorb 42% more calcium from the modified carrots than from normal carrots.

There have been several experiments of genetic modification in order to fight abiotic stress with the purpose of increasing frost resistance, drought resistance or the resistance against flooded fields.

Bananas are an important source of calories for many people. However, they are vulnerable to new kinds of diseases. Thus, a pepper gene has been inserted in bananas in order to make them more resistant.

Transferring a gene from a decorative plant into a tomato not only changed the color of the tomato from red to purple, it also enabled the tomato to produce anthocyanin, which prevented mice from getting cancer.

When cutting an apple and leaving it untouched for a while, it usually turns brown. There have been attempts from industries to create a sort of apples called Artic apple, which will no longer turn brown after cutting.

Genetic engineering is a quite controversial topic in our society. It has many advantages and fields of application, but can also have detrimental effects on humans as well as on the whole ecological system.

There are also many religious and ethic concerns against the use of gene manipulation. Thus, as humans, we have to make difficult decisions in the future on whether we want to play god in order to be able to fight deadly diseases or if we do not want to take the risk.

Sources

http://www.fao.org/3/Y5160E/y5160e10.htm#P3_1651The

http://www.fao.org/3/y4955e/y4955e06.htm

https://en.wikipedia.org/wiki/Genetic_engineering

About the author

My name is Andreas and my mission is to educate people of all ages about our environmental problems and how everyone can make a contribution to mitigate these issues.

As I went to university and got my Masters degree in Economics, I did plenty of research in the field of Development Economics.

After finishing university, I traveled around the world. From this time on, I wanted to make a contribution to ensure a livable future for the next generations in every part of our beautiful planet.

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Genetic Engineering: Pros & Cons - E&C

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Engineering a far-red lightactivated split-Cas9 system for remote-controlled genome editing of internal organs and tumors – Science Advances

Friday, July 10th, 2020

INTRODUCTION

Many studies have shown that the CRISPR-Cas9 system is a revolutionary technology (1, 2). This relatively easy-to-use technology has provided unprecedented opportunities for scientific research and disease treatments, including applications in high-throughput screening and functional genomics research and treatment of virus infections (3), genetic diseases (4), and cancer (5). Nevertheless, there are now several well-known disadvantages with the CRISPR-Cas9 system, including the fact that single guide RNAs (sgRNAs) can sometimes lead to off-target effects such as double-strand breaks in untargeted genome regions, which can cause unintended adverse consequences such as gene mutations, insertions, deletions, and even tumorigenic events (6). Seeking to overcome these challenges, several strategies have been developed to improve the precision of CRISPR-Cas9 gene editing, including Cas9 modifications (e.g., Cas9 nickase and high-fidelity variants), prime editors, base editors, and selecting sgRNAs with minimal off-target capacity (7, 8). Recently, some inducible Cas9 expression systems have been developed to limit the activity or lifetime of Cas9, thereby lowering the probability of off-target effects by reducing the exposure time of a cells genome to the Cas9 nuclease (9).

There are a variety of chemically induced CRISPR-Cas9 systems, including doxycycline-regulated Cas9 (10), trimethoprim (TMP) (11) and 4-hydroxytamoxifen (4-OHT)controlled Cas9 (12), rapamycin-inducible split-Cas9 (13), 4-OHTresponsive inteindependent Cas9 (14), and 4-OHTresponsive nuclear receptors split-Cas9 (15), among others. However, a notable adverse effect of these systems is the potential for cytotoxicity from the chemical inducers: Doxycycline can negatively affect cell numbers and colony formation (16), TMP can inhibit uptake of folic acid by the cells (17), 4-OHT can increase cytosolic levels of autophagosomes and cause irregularly clumped chromatin in the nuclei (18), and rapamycin can perturb the endogenous mammalian target of rapamycin pathway (19). Moreover, once these agents are inside the cells or present in an in vivo context, these inducer chemicals can diffuse freely, limiting the spatial resolution of editing induction. In addition, it is difficult to rapidly remove the inducer compounds, so they can persist for a long time, making it difficult to turn Cas9 activity on and off quickly and precisely.

These limitations have helped motivate the development of multiple systems based on the optical control of Cas9 activity because light is a reversible and noninvasive inducer modality that potentially offers fine precise spatiotemporal resolution. The first reported example of a photoactivatable Cas9 system was paCas9 system based on blue light (20). In the paCas9 system, Cas9 nucleases are fragmented into two nonfunctional fragments that can be reconstituted as an active nuclease under blue light illumination based on dimerization of their respective fusion domains, the positive Magnet (pMag) or negative Magnet (nMag) proteins from the filamentous fungus Neurospora crassa (21). Later studies reported the ultraviolet (UV) lightmediated cleavage of a synthesized complementary oligonucleotide element that normally inactivates the editing-guiding function of sgRNAs (22).

There is also a recently reported blue lightbased anti-CRISPR system comprising AcrIIA4 (23) (a potent Cas9 inhibitor) and the LOV2 blue-light photosensor (24). Without illumination, the AcrIIA4-LOV2 complex remains bound to Cas9, inhibiting its nuclease activity. Under blue light illumination, the AcrIIA4-LOV2 complex is separated from Cas9 and its editing activity can be restored (25). However, neither UV nor blue light is able to penetrate deeply into the body, owing to the strong absorption and scattering of these light energies by biological tissues (26). UV light hardly penetrates the skin and blue light does merely by 1 mm (27, 28). This substantial limitation, viewed alongside the fact that UV and prolonged blue light exposure can cause cytotoxicity (29, 30), highlights the difficulty of applying these light-induced Cas9 systems for in vivo research applications and clinical translation.

We have, for some time, been investigating far-red light (FRL)inducible genetic systems due to the deep tissue penetration of FRL with above 5 mm beneath the surface of skin (27, 28). We here report our development of an FRL-activated split-Cas9 (FAST) system that can be used to noninvasively induce gene editing activity in cells located deep inside animal tissues. The FAST system relies on two split-Cas9 fusion proteins with high-affinity binding domains: One half of Cas9 is constitutively expressed, while the other is under the FRL-inducible control of the bacterial phytochrome BphS optical controllable system previously established by our group (31). We initially assembled the FAST system components in human embryonic kidney (HEK)293 cells and used light-emitting diode (LED)based FRL illumination to demonstrate successful activation of targeted genome editing. Next, after achieving FRL-inducible editing in diverse human cell lines, experiments with implants confirmed that FAST was able to robustly activate editing in cells positioned in subdermal animal tissues. Experiments with the transgenic tdTomato reporter mouse line established FRL-induced FASTmediated editing of mouse somatic cells (hepatocytes in the liver), and work with cell cycleinactivating gene edits of cancer cells in xenograft tumor mice demonstrate how FAST can be deployed against disease. Thus, beyond extending the optogenetic toolbox for gene editing of mammalian cells to include induction by the highly in vivocompatible and deep tissuepenetrating energies of FRL, our study extends this initial technology to demonstrate applications relevant for basic biological and biomedical research.

To develop an optogenetically controlled device for genome editing with deep tissuepenetrative capacity and with negligible phototoxicity in vivo, first, we constructed an FRL-controlled full-length Cas9 system based on our previously reported orthogonal FRL-triggered optogenetic system (FRL-v2) (31). However, there was serious background leakage in dark state with low-induction performance under illumination. Therefore, we focused on building a FAST system based on split-Cas9 (13) and FRL-v2, which comprises the bacterial FRL-activated cyclic diguanylate monophosphate (c-di-GMP) synthase (BphS) and a c-di-GMPresponsive hybrid transactivator, p65-VP64-BldD. For the FAST system, we then fused the N-terminal Cas9 fragment [Cas9(N)] to the Coh2 domain from Clostridium thermocellum (32) and fused the C-terminal Cas9 fragment [Cas9(C)] to the DocS domain from the same bacterium. Expression of the NLS-Cas9(N)-Coh2 fusion protein is driven by the FRL-v2specific chimeric promoter (PFRL), while expression of the DocS-Cas9(C)-NES fusion protein is driven by a constitutive promoter (PhCMV). A complete Cas9 protein can be reconstituted upon FRL illumination because of the high-affinity interaction of the Coh2 and DocS domains (Fig. 1). Confirming the editing activity of the reconstituted Cas9, we found that HEK-293 cells cotransfected with pXY137 (PhCMV-p65-VP64-BldD-pA::PhCMV-BphS-P2A-YhjH-pA, 100 ng), pYH20 [PFRL-NLS-Cas9(N)-Linker-Coh2-pA, 50 ng], pYH102 [PhCMV-DocS-Linker-Cas9(C)-NES-pA, 100 ng], and pYW57 [PU6-sgRNA (CCR5)-pA, 50 ng] successfully edited the targeted human CCR5 locus (11.9% indel frequency) upon FRL illumination (1 mW/cm2; from an LED source, 730 nm); no editing was detected for dark control cells (Fig. 2, A and B). These detected edits were analyzed by the mismatch-sensitive T7 endonuclease I (T7E1) assay. We further used Sanger sequencing to confirm that the FRL-induced, FAST-mediated edits (indel mutations) occurred in the targeted region of the human CCR5 locus at a frequency of ~20% using the tracking of indels by decomposition (TIDE) analysis (fig. S1).

(A) Schematic of the split-Cas9 fusion protein components of the FAST system. Coh2 and DocS are two C. thermocellum proteins that interact with high affinity. Cas9 is formed from two separate (N- and C-terminal) Cas9 fragments that individually lack nuclease activity. When Cas9s two fragments Cas9(N) and Cas9(C) are respectively fused with Coh2 and DocS, they readily combine to reconstitute a nuclease-active form of Cas9. (B) Schematic of the FAST system, as deployed in mammalian cells, based on the fragments detailed in (A). FRL (~730 nm) activates the engineered bacterial photoreceptor BphS, which converts guanosine triposphate (GTP) into c-di-GMP. c-di-GMP can bind to BldD (derived from sporulating actinomycete bacteria) and be translocated into the nucleus. This induces dimerization of the synthetic transcriptional activators p65-VP64-BldD [BldD fused with p65 (the nuclear factor Btransactivating domain) and VP64 (a tetramer of the herpes simplex virusderived VP16 activation domain)], after which they bind to PFRL to activate expression of the N-terminal fusion fragment of split-Cas9. The other (C-terminal) fusion fragment is constitutively expressed, as driven by the human cytomegalovirus promoter (PhCMV). DNA double-strand breaks are formed by Cas9 after the Coh2-DocS heterodimerizationmediated reconstitution of the two fusion fragments.

(A) Time schedule of FRL-controlled gene editing in HEK-293 cells. Cells were illuminated (1 mW/cm2; 730 nm) for 4 hours once a day for 2 days and were collected at 48 hours after the first illumination for further analysis. (B) A mismatch-sensitive T7 endonuclease I (T7E1) assay to test HEK-293 cells (6 104) transfected with full-length Cas9 (pHP1) or the FAST system (pXY137, pYH20, and pYH102), together with the sgRNA targeting to CCR5 locus (pYW57). FRL-mediated editing (indel deletions) of the human EMX1, CXCR4, and VEGFA loci by FAST was performed using the same experimental procedure as that used when targeting the CCR5 gene. (C) FRL-mediated multiplex editing of the human CCR5 and CXCR4 loci. (D) FAST-mediated DNA insertion via homology-directed repair (HDR), achieved by adding a single-stranded oligodeoxynucleotide (ssODN) template (10 M), bearing a HindIII restriction endonuclease site. Homologous arms are indicated in red. The target sites of sgRNA (EMX1) are marked in blue. HEK-293 cells (6 104) were cotransfected with full-length Cas9 (pHP1) or the FAST system (pXY137, pYH20, and pYH102) and the sgRNA targeting to EMX1 locus (pYH227) via a nucleofection method. In (B) to (D), n = 2 from two independent experiments. Red arrows indicate the expected cleavage bands. Detailed description of genetic components and transfection mixtures are provided in tables S1 and S5. N.D., not detectable.

We next confirmed that the FAST system can cleave different targeted endogenous genomic loci and induce indel mutations via nonhomologous end joining (NHEJ) in an FRL-dependent manner by designing sgRNAs targeting three additional human genes (EMX1, CXCR4, and VEGFA), and these induced indel mutations were detected by T7E1 assay. With each of these sgRNAs, FRL-induced but not dark-induced indel mutations were observed (Fig. 2B). We also confirmed that the FAST system can cleave targeted exogenous d2EYFP reporter efficiently (fig. S2). In addition to single gene targeting, we also tested whether our FAST system can simultaneously edit multiple target sites. Using one sgRNA targeting CCR5 and another sgRNA targeting CXCR4, the FAST system was capable of inducing the desired indel mutations at the two target sites upon FRL illumination (Fig. 2C), demonstrating optogenetic multiplexed control of NHEJ-mediated indel mutations in mammalian cells.

We further investigated whether FAST can be used for homology-directed repair (HDR)mediated genome editing. The FAST system components and a donor template (single-stranded oligodeoxynucleotide containing a HindIII site) were electroporated into HEK-293 cells. Assessment of HDR events at the EMX1 locus using restriction endonuclease assays showed that the FAST system induced HindIII site integration at the EMX1 locus at a frequency of 5.7% under FRL illumination; no HDR events were detected in dark controls (Fig. 2D). Together, these results establish that the FAST system can be deployed for optogenetic control of NHEJ-/HDR-mediated indel mutations.

To demonstrate photoactivatable regulation of gene editing in diverse mammalian cell lines, we introduced the FAST system into four different human cell lines, and it achieved successful FRL-induced gene editing (CCR5 locus) in each of them (Fig. 3A). Next, experiments testing the FRL illumination intensity and duration-dependent activity of the FAST system showed that the frequency of edits (indel mutations at CCR5) increased along with illumination intensity and with illumination time (Fig. 3, B and C), indicating the tunability of the FAST system. We also used a photomask to establish proof of principle for spatially controlled gene editing with the FAST system (Fig. 3, D and E). We also conducted an experiment with two rounds of FRL illumination to verify repeated induction cycles of the FAST system wherein the first round of illumination achieved indel mutations guided by an sgRNA targeting CXCR4 locus, followed by transfection of a second sgRNA targeting the CCR5 locus, which guided successful indel mutations after the second FRL illumination. However, engineered cells shifted to the dark did not have indel mutations in CCR5 locus (fig. S3, A and B). This result indicates that the FAST system is reusable and reversible.

(A) FAST-mediated gene editing in four human cell lines. (B) Illumination intensitydependent FAST gene editing. In (A) and (B), cells were collected for mismatch-sensitive T7E1 assays, as indicated in the time schedule of Fig. 2A. (C) Evaluation of exposure timedependent FAST system gene editing performance. Cells were collected for T7E1 assays at 24 hours after the start of the second illumination. (D) Schematic of the photomask device used to demonstrate the spatial regulation of FAST-mediated gene editing. Cells were illuminated through a photomask containing a 7-mm line pattern. (E) Spatial control of FRL-dependent gene editing mediated by the FAST system. HEK-293 cells (3 106) were cotransfected with the FAST system, sgRNA (pYW57), and a frameshift enhanced green fluorescent protein (EGFP) reporter containing a CCR5 locus (pYH244) and were illuminated with FRL (0.5 mW/cm2; 730 nm; 2-min on, 2-min off) for 48 hours. EGFP is not expressed without Cas9 activity because the EGFP sequence is out of frame. Upon double-strand cleavage by Cas9, the frameshifts caused via DNA repair by NHEJ enable EGFP expression. The fluorescence of EGFP was assessed via fluorescence meter ChemiScope 4300 Pro imaging equipment (Clinx) at 48 hours. In (A) to (C), n = 2 from two independent experiments. Red arrows indicate the expected cleavage bands. Detailed description of genetic components and transfection mixtures are provided in tables S1 and S5. SEAP, human placental secreted alkaline phosphatase.

We then evaluated the photocytotoxicity of FRL (730 nm) or blue light (470 nm) illumination on mammalian cells. When HEK-293cells were transfected with human placental secreted alkaline phosphatase (pSEAP2)-control-and then exposed to FRL or blue light for different intensity, the SEAP expression demonstrated that the FRL exposure resulted in negligible cytotoxicity. However, a marked difference was observed from the blue light illumination, which substantially reduced cell viability (fig. S4, A and B). Moreover, we did not observe substantially increased cytotoxicity with FRL illumination of cells engineered with the FAST system (fig. S4, C and D), indicating the inertness and noncytotoxicity of the system constituents. In short, neither FRL illumination nor the ectopic presence of FAST system constituents was verified to influence the gene expression capacity of the engineered cells. In addition, we also compared the controllable gene editing performance of our FAST system with the rapamycin-responsive split-Cas9 system (13) and the blue lightcontrolled paCas9 system (20) that have been reported. The results showed that the genome editing efficiency of rapamycin-responsive split-Cas9 system was lower than the FAST system (fig. S5, A and B), and the paCas9 system had relative higher background leakage in the dark. Our FAST system showed notable induction of indel mutations under FRL illumination but with negligible background in the dark (fig. S5, C and D). Off-target activity of the FAST system was also assessed simply. We checked a potential off-target site of human BMP1 locus, as reported previously (33). The indel frequencies were determined through T7E1 assay at the on-target and potential off-target sites of BMP1. As a result, no mutations were detected at the potential off-target site after editing by our FAST system (fig. S6, A and B). This is probably due to the FAST-mediated transient expression of split-Cas9 that lowered the probability of off-target effects by reducing the exposure time of a cells genome to the Cas9 nuclease (79). However, there might be off-target effects that can still occur in illuminated cells.

Having established the basic performance characteristics of the FAST system in human cells, we next conducted experiments with mice to verify the systems capacity to induce gene editing based on the tissue-penetrating capacity of FRL. Specifically, we conducted an experiment using hollow fiber implantation of HEK-293 cells equipped with the FAST system into the dorsum of mice and exposed to FRL illumination (10 mW/cm2; alternating 2-min on/off for 4 hours) (Fig. 4A). Notably, the FRL illumination of the FAST cell-bearing mice induced notable activation of gene editing (~11.4% of the cells retrieved from the implant fibers was edited at the CCR5 locus versus not detectable for dark control cells) (Fig. 4B). These results demonstrate that the FAST system can be used to activate gene editing inside animal tissues, exploiting the physical properties of FRL as an inducer modality.

(A) Schematic for the time schedule and experimental procedure for FRL-controlled gene editing in mice harboring hollow fiber implants with HEK-293 cells. Pairs of 2.5-cm hollow fibers containing a total of 5 106 transgenic HEK-293 cells (engineered with FAST system) were subcutaneously implanted on the dorsum of wild-type mice and illuminated with FRL (10 mW/cm2; 730 nm; 2-min on, 2-min off) for 4 hours each day for 2 days. Cells were collected from the hollow fiber implants at 48 hours after the first illumination and assessed with mismatch-sensitive T7E1 assay to assess targeted gene editing efficiency (CCR5 locus). (B) Representative T7E1 assay for FAST-mediated indel mutations. n = 3 mice. The red arrow indicates the expected cleavage bands. Detailed description of genetic components and transfection mixtures are provided in table S1 and S5.

We obtained transgenic mice harboring a homozygous Rosa26 CAG [cytomegalovirus (CMV) enhancer fused to the chicken beta-actin] promoter loxP-STOP-loxP-tdTomato cassette present in all cells. In this model, tdTomato is silent because of the stop signal [three repeats of the simian virus 40 (SV40) polyadenylate (polyA) sequence], but the deletion of the stop cassette allows transcription of the tdTomato gene, resulting in fluorescence expression. The Cas9-mediated DNA cleavage of the stop sequence guided by sgRNAs can initiate CAG promoter to drive tdTomato expression (34). Therefore, we used this mouse model to examine the in vivo genome editing performance of the FAST system in mice somatic cells (Fig. 5A). We used hydrodynamic injection to introduce the FAST system components, along with an sgRNA designed to target the deletion of the SV40 polyA stop cassette, which should activate tdTomato reporter protein expression upon successful editing. Note that it is difficult to activate tdTomato expression by Cas9 system as the desired edit requires two cuts on the same allele; we eventually achieved the desired edit, but it required optimization of the delivery mode for the FAST components. Briefly, we chose hydrodynamic injection because it is known to result in enrichment of plasmids (and thus, transgene expression) in liver cells (35). We reduced the overall number of plasmids by combining some constructs (fig. S7, A and B) and explored a number of different injection time and illumination schedules (Fig. 5A), but we only detected weak tdTomato signals in the FRL-illuminated FAST mice (fig. S8).

(A) Schematic showing the time schedule and experimental procedure for assessing in vivo gene editing. The minicircle iteration of the FAST system pYH412, pYH413, and pYH414 at a 7:15:4 (w/w/w) ratio were injected hydrodynamically via tail vein. Twenty-four hours after injection, mice were illuminated with FRL (10 mW/cm2; 730 nm; 2-min on, 2-min off) for 4 hours per day for 3 days. A second injection of the minicircle-based FAST system components was performed on the fifth day, followed by 4 hours daily illumination for three additional days. In our design, the tdTomato reporter protein was expressed after a stop cassette was destroyed by Cas9 editing. (B) Fluorescence IVIS image of mouse livers. (C) The frequency of edits (targeting the aforementioned stop cassette) by monitoring fluorescence intensity of the tdTomato reporter in Gt(ROSA)26Sortm14(CAG-tdTomato)Hze mice. (D) Representative fluorescence microscopy images of tdTomato and tdTomato+ hepatocytes present in frozen liver sections from FRL-illuminated mice. Blue indicates 4,6-diamidino-2-phenylindole (DAPI) staining nuclei; red indicates endogenous tdTomato expression. The images represent typical results from three independent measurements. Scale bar, 100 m. Data in (C) are means SEM; n = 3 mice. P values were calculated by Students t test. ****P < 0.0001 versus control.

We speculated that this apparently weak induction of editing activity may result from rapid degradation of the plasmids, so we constructed minicircle (36) iterations of our FAST system. Minicircle DNA vectors without the bacterial backbone of the plasmid, markedly reducing the possibility of random integration of bacterial DNA sequences into the genome, have been shown to maintain gene expression in cells for long durations because these molecules are resistant to degradation (37). We delivered the minicircle iterations of the FAST via hydrodynamic injection and used FRL illumination schedules as follows: alternating 2-min on/off for 4 hours, once each day for 3 days; we then monitored the fluorescence signal intensity in livers. FRL illumination of the mice bearing the FAST system resulted in strong editing and thus, tdTomato reporter expression (Fig. 5, B and C). We also detected strong tdTomato expression in liver sections prepared from the FRL-illuminated FAST mice (Fig. 5D), and Sanger sequencing of genomic DNA extracted from the livers verified the success of the targeted excision of the SV40 polyA stop cassette in the FRL-induced FAST mice (fig. S9). Collectively, these results demonstrate that the FAST system can be used for in vivo editing of the genomes of somatic cells located in the internal organs of mice.

We further investigated the optogenetic activation of the FAST system in tumor models as proof-of-concept examples for therapeutic genome editing. The polo-like kinase (PLK1) protein is a highly conserved serine-threonine kinase that promotes cell division, and strong PLK1 expression is a marker in various types of tumor (38). Extensive work has established that inhibition or depletion of PLK1 leads to cell-cycle arrest, apoptosis, and a so-called mitotic catastrophe in cancer cells, which provides a promising modality for anticancer therapy (39, 40). After initially confirming that the FAST system can edit the PLK1 locus (indel mutations and extensive apoptosis) in the FRL-illuminated human lung cancer A549 cells in vitro (fig. S10, A to D), we then evaluated the tumor therapy application of our FAST system by testing the in-tumor editing performance of the FAST system for the disruption of the PLK1 locus in mice bearing A549 xenograft tumors.

We first delivered the minicircle iterations of the FAST system alongside a PLK1-targeting sgRNA minicircle vector when the tumors had reached 80 to 100 mm3; note that we also injected transfection reagent, a cationic polymer-coated nanoparticle (APC), (41) to facilitate the transfection of tumor cells in situ. Subsequently, FRL illumination was delivered to the xenograft-bearing mice via LED for 4 hours each day for 7 days (Fig. 6A), and tumor development was monitored by measuring the sizes of the tumors every 2 days. Notable inhibition of tumor growth was observed for the FAST mice that received FRL illumination; no such inhibition was observed for the dark control FAST or FRL-illuminated vehicle control mice (Fig. 6, B to D). Mismatch-sensitive T7E1 assays confirmed that the FRL-induced FAST system achieved the desired genome disruption of PLK1 gene in the tumor tissue (Fig. 6E) at a frequency of ~21.5% detected by TIDE analysis (Fig. 6F). Moreover, quantitative real-time polymerase chain reaction (qRT-PCR) verified the expected reductions in tumor PLK1 mRNA expression upon FRL illumination (Fig. 6G). Consistent with the observed antitumor efficacy, subsequent histologic analysis of tumor sections revealed extensive cancer cell necrosis (Fig. 6H) and very extensive cell apoptosis [via both terminal deoxynucleotidyl transferasemediated deoxyuridine triphosphate nick end labeling (TUNEL) and caspase-3labeling assays; Fig. 6, I and J]. Thus, FRL-triggered FAST-mediated gene editing can inhibit cancer cell growth in xenograft tumors in mice. These results further indicate that our FAST system could be deployed for deep tissue gene editing.

(A) Schematic showing the time schedule and experimental procedure for the in-tumor FAST-mediated gene editing. The minicircle iteration of the FAST system targeting to PLK1 locus pYH412, pYH420, and pYH414 at a 7:15:4 (w/w/w) ratio were injected intratumorally. Twenty-four hours after per injection, mice were illuminated with FRL (10 mW/cm2; 730 nm; 2-min on, 2-min off) for 4 hours per day totally for 7 days. (B) Images of tumor tissues from the different treatments. (C) Tumor growth curves for the different treatments. (D) The weight of tumor tissues after the different treatments. (E) Indel mutations in the tumor tissues detected via mismatch-sensitive T7E1 assays. Red arrows indicate the expected cleavage bands. (F) The gene editing efficacy quantified by the TIDE analysis. (G) Relative mRNA expression levels of the PLK1 gene quantified by quantitative real-time polymerase chain reaction (qRT-PCR). The data are means SEM; n = 5 mice. P values were calculated by Students t test. ****P < 0.0001 versus control. (H) Representative fluorescence microscopy images of hematoxylin and eosin (H&E) staining of tumor tissues. The images represent typical results from three independent measurements. Scale bar, 100 m. Representative fluorescence microscopy images of TUNEL staining (I) and caspase-3 (J) staining of tumor tissues. The images represent typical results from three independent measurements. Scale bars, 100 m. Photo credit: Yuanhuan Yu, East China Normal University.

CRISPR-Cas9 is an undeniably revolutionary technology that is changing biological and medical research (4, 5, 42), and several innovative extensions of the basic CRISPR-Cas9 concept have enabled a new era of conditional genome editing activation iterations with chemical (1015) and UV/blue light inducers (20, 22, 25). Nevertheless, limitations with these systems warrant the development of alternatives that exploit different induction sources. The FAST system we developed in the present study opens the door for spatiotemporally selective induction of Cas9 genome editing deep inside animal tissues. It bears emphasis that our induction uses LED lights rather than lasers or optical fibers, highlighting that FAST should be very easy to deploy in a wide range of experimental contexts. Although we did face initial hurdles with induction efficiency for in vivo applications, our development of a minicircle-based iteration of the FAST system easily overcame this and permitted robust editing in mouse livers. The deep tissuepenetrating utility of the FAST system was applied to achieve anticancer therapy by disrupting PLK1 gene in mice bearing A549 xenograft tumors. In this way, we could greatly reduce side effects of the anticancer drugs and promote the precision treatment of cancers. We also envision that the FAST system can be used to study the function of cancer-associated genes during tumor development process by controlling gene knockout or interference in specific tissues at different time nodes.

While we do demonstrate FAST system applications for biological research and the treatment of disease, the present paper merely reports the initial proof-of-principle study. Given that FAST is a fully genetically encoded system, a variety of vectors, alternative plasmids, and tissue-specific promoters could be used to selectively deliver FAST system components to diverse tissues, and we fully anticipate that adeno-associated virus vectors will become a popular modality for this task. Moreover, there is no obvious factor to prevent the deployment of FAST as a genome-integrated stable system, which should enable researchers to selectively activate targeted editing anywhere that they are able to supply sgRNAs and FRL illumination from an LED.

We anticipate that the combination of precise temporal control and deep tissue penetration will enable rapid-uptake FAST in a variety of research communities. Chemical inducers can cause adverse effects in cells and can diffuse freely, and the complexity of cellular and organismal metabolism makes it exceedingly difficult to precisely control the spatiotemporal dynamics of inducible gene editing systems (1619). In this light, perhaps researchers can deploy FAST and FRL induction strategies to explore the development, basic biology, or etiopathological basis of diverse processes that occur in animal internal organs such as the heart, lungs, liver, kidneys, etc., and in tissues, including muscles and bone marrow. In theory, the FAST system should give researchers previously unattainable precise control of conditional genetic knockout and knock-in experiments. A huge variety of temporal illumination schemes should be feasible with FAST because FRL has low phototoxicity, representing a clear advantage over UV- and blue lightbased Cas9 induction systems. Moreover, FAST may offer neuroscientists an alternative to the presently popular optical fiber implantationbased approaches for optogenetic-based gene editing research.

In summary, we have developed a FAST system that is apparently safe (negligible phototoxicity to mammalian cells, high tissue permeability, and noninvasiveness). With FRL as its fundamental basis, the FAST system offers excellent tunability (robust induction of gene editing and almost negligible background activity) and precise controllability (illumination intensity dependent, exposure time dependent, and strong spatiotemporal specificity), making it suitable and practical for the many biological and biomedical applications that require gene editing in vivo, especially for processes that occur within animal tissues.

The FAST system consists of the following main components: the FRL sensors (BphS and p65-VP64-BldD) (31), interacting proteins (cohesion Coh2 and dockerin DocS from C. thermocellum) (32), and the N- and C-terminal fragments of Streptococcus pyogenes Cas9 [Cas9(N) (residues 2 to 713) and Cas9(C) (residues 714 to 1368)] (13). Complementary DNAs (cDNAs) encoding BphS and p65-VP64-BldD were prepared, as previously described (31). cDNAs encoding Coh2 and DocS were chemically synthesized by the company Genewiz Inc. cDNAs encoding the N- and C-terminal fragments of Cas9 fused with a nuclear localization signal from SV40 T antigen were amplified from the Addgene plasmid 42230. The inducible Cas9 was constructed on the basis of the Cas9(N) and Cas9(C) fragments fused with Coh2 and DocS, respectively, which were cloned through Gibson assembly according to the manufacturers instructions [Seamless Assembly Cloning Kit; catalog no. BACR(C) 20144001; OBiO Technology Inc.]. All genetic components have been validated by sequencing (Genewiz Inc.). Plasmids constructed and used in this study are provided in table S1.

The sgRNAs targeting CCR5, EMX1, CXCR4, VEGFA, BMP1, tdTomato stop cassette, and PLK1 were generated by annealed oligos and cloned into the BbsI site of a constitutive mammalian PU6-driven sgRNA expression vector (pYH49). The PU6-sgRNA fragment was PCR amplified from the Addgene plasmid 58767 and then cloned into the corresponding sites (MluI/XbaI) of pcDNA3.1(+) to obtain the pYH49 expression vector. The target sequences and oligonucleotides used for sgRNA construction are listed in table S2.

All cell types {HEK-293 [CRL-1573; American Type Culture Collection (ATCC)], HeLa (CCL-2; ATCC), telomerase-immortalized human mesenchymal stem cells (43), and HEK-293derived Hana3A cells engineered for constitutive expression of RTP1, RTP2, REEP1, and Go} were cultured at 37C in a humidified atmosphere, containing 5% CO2 in Dulbeccos modified Eagles medium (DMEM; catalog no. C11995500BT; Gibco) supplemented with 10% fetal bovine serum (FBS; catalog no. 16000-044; Gibco) and 1% (v/v) penicillin/streptomycin solution (catalog no. ST488-1/ST488-2; Beyotime Inc.). All cell lines were regularly tested for the absence of mycoplasma and bacterial contamination. Cells were transfected with an optimized polyethyleneimine (PEI)based protocol (44). Briefly, cells were seeded in a 24-well cell culture plate (6 104 cells per well) 18 hours before transfection and were subsequently cotransfected with corresponding plasmid mixtures for 6 hours with 50 l of PEI and DNA mixture [PEI and DNA at a ratio of 3:1 or 5:1 (w/w)] (PEI molecular weight, 40,000; stock solution of 1 mg/ml in ddH2O; catalog no. 24765; Polysciences Inc.). At 12 hours after transfection, the culture plate was placed below a custom-designed 4 6 LED array (1 mW/cm2; 730 nm) for illumination.

For HDR-mediated genome editing experiments, 6 105 HEK-293 cells were nucleofected with the FAST system plasmids (pXY137, 200 ng; pYH20, 100 ng; and pYH102, 200 ng), sgRNA expression vector (pYH227, 100 ng; targeting EMX1), and 10 M single-stranded oligonucleotide donor using the SF Cell Line 4D-Nucleofector X Kit L (catalog no. V4XC-2024; Lonza) and the CM-130 program (4D-Nucleofector System; Lonza). At 24 hours after nucleofection, cells were illuminated by FRL (1 mW/cm2; 730 nm) for 4 hours once a day for 2 days, and then cells were collected at 48 hours after the first illumination for analysis. Genomic DNA was isolated using a TIANamp Genomic DNA Extraction Kit (catalog no. DP304; TIANGEN Biotech Inc.) according to the manufacturers instructions.

Genomic DNA was extracted from cells or tissues using the TIANamp Genomic DNA Extraction Kit (catalog no. DP304; TIANGEN Biotech Inc.) according to the manufacturers instructions. The genomic region containing the target sites was PCR amplified using the 2 Taq Plus Master Mix II (Dye Plus) DNA polymerase (catalog no. P213; Vazyme Inc.). The primers used for PCR amplification are listed in table S3. The PCR amplicons were purified using HiPure Gel Pure Micro Kits (catalog no. D2111-03; Magen Inc.) according to the manufacturers protocol. Purified PCR products (300 ng) were mixed with 1.5 l of 10 M buffer for restriction enzyme (catalog no.1093A; Takara Bio) and ultrapure water to a final volume of 15 l and reannealed (95C, 5 min; 94C, 2 s, 0.1C per cycle, 200 times; 75C, 1 s, 0.1C per cycle, 600 times; and 16C, 5 min) to form heteroduplex DNA. After reannealing, the heteroduplexed DNA was treated with 5 U of T7E1 (catalog no. M0302; New England BioLabs) for 1 hour at 37C and then analyzed by 1.5% agarose gel electrophoresis. Gels were stained with GelRed (catalog no. 41003; Biotium) and imaged with Tanon 3500 gel imaging system (Tanon Science & Technology Inc.). Relative band intensities were calculated by ImageJ software. Indel percentage was determined by the formula 100% [1 (1 (b + c)/(a + b + c))1/2], in which a is the integrated intensity of the undigested PCR product, and b and c are the integrated intensities of each cleavage product.

Sequence of the gene region containing the target sequence was amplified by PCR. Purified PCR amplicons from the nuclease target site were cloned into the T-vector pMD19 (catalog no. 3271; Takara Bio). Thirty clones were randomly selected and sequenced using each genes PCR forward primers by the Sanger method (45). Primers used for PCR amplification are listed in table S3.

Target regions were amplified by PCR. Purified PCR samples were analyzed by Sanger sequencing. The sequencing data files (.ab1 format) were imported into the TIDE Web tool (https://tide.nki.nl/) (46) to quantify nature and frequency of generated indels.

The genomic PCR and purification were performed, as described above. Purified PCR products were mixed with 15 U of HindIII (catalog no. 1060B; Takara Bio), 2 l of 10 M buffer for restriction enzyme, and ultrapure water to a final volume of 20 l and then incubated at 37C for 3 hours. The digested products were analyzed by agarose gel electrophoresis. Gel staining and imaging were performed, as described above. Quantification was calculated on the basis of relative band intensities. The HDR percentage was determined by the formula 100% (b + c)/(a + b + c), in which a is the intensity of the undigested PCR product, and b and c are the intensities of each HindIII-digested product.

HEK-293 cells (6 104) were cotransfected with the FAST system (pXY137, 100 ng; pYH20, 50 ng; and pYH102, 100 ng), the sgRNA targeting d2EYFP (pYH410, 50 ng), and the d2EYFP reporter plasmid (pYW110, 200 ng). At 12 hours after transfection, cells were illuminated (1 mW/cm2; 730 nm) for 4 hours once a day for 2 days and were harvested after trypsinization and washed in phosphate-buffered saline (PBS) for three times. About 10,000 events were collected per sample and analyzed with a BD LSRFortessa cell analyzer (BD Biosciences) equipped for d2EYFP [488-nm laser, 513-nm longpass filter, and 520/30 nm emission filter (passband centered on 530 nm; passband width of 30 nm)] detection. Data were analyzed using the FlowJo V10 software.

The production of human placental SEAP in cell culture medium was quantified using a p-nitrophenylphosphatebased light absorbance time course assay, as previously reported (31). Briefly, 120 l of substrate solution [100 l of 2 SEAP buffer containing 20 mM homoarginine, 1 mM MgCl2, and 21% (v/v) diethanolamine (pH 9.8) and 20 l of substrate solution containing 120 mM p-nitrophenylphosphate] were added to 80 l of heat-inactivated (65C, 30 min) cell culture supernatant. The time course of absorbance at 405 nm was measured by using a Synergy H1 hybrid multimode microplate reader (BioTek Instruments Inc.) installed with the Gen5 software (version 2.04).

Cell viability was assayed using an MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] cytotoxicity assay kit (catalog no. E606334-0250; Sangon Biotech Inc.) according to the manufacturers instructions. Briefly, 10 l of MTT reagent (5 mg/ml) was added to each well of 96-well plates. The samples were mixed gently and incubated for 4 hours in a CO2 incubator. Formazan solubilization solution (100 l) was added into each well. The plate was put on a shaker to mix gently for 10 min to dissolve the formazan crystals, and then the plate was read with a Synergy H1 microplate reader (BioTek Instruments Inc.) at 570 nm.

The off-target sites of the BMP1 gene were examined according to the previously reported procedure (33). Genomic DNA was extracted, as described above, and the region of genome containing the possible nuclease off-target sites was PCR amplified using appropriate primers (table S3). The following procedures were similar to those of on-target examination by T7E1 assay, as described above.

Minicircles are episomal DNA vectors that allow sustained transgene expression in quiescent cells and tissues. Minicircle DNA vectors were prepared, as previously described (36). Minicircle-producing system contains the Escherichia coli strain ZYCY10P3S2T (a genetically modified minicircle-producing bacterial strain) and the empty minicircle-producing plasmid pMC.BESPX (gene of interest would be cloned into this plasmid). Briefly, ZYCY10P3S2T competent cells prepared with standard protocol, as previously described (36), were transformed with the minicircle-producing plasmid pMC.BESPX carrying the gene of interest. The transformed cells were cultured and induced by 0.01% l-arabinose to produce minicircle DNA vectors that were devoid of the bacterial plasmid DNA backbone and contain only genes of interest.

The in vivo DNA delivery reagent APC is a cationic polymer-coated nanoparticle composed of biocompatible polystyrene sulfonate and -cyclodextrinPEI (Mw, 25 kDa) and prepared, as previously reported (41). First, the seed solution was prepared by adding freshly prepared 600 l of NaBH4 (10 mM) into 5-ml mixture of HAuCl43H2O (0.5 mM) and cetyltrimethylammonium bromide (CTAB; 0.1 M) and incubated at 30C for 30 min. Ten milliliters of HAuCl43H2O (1 mM), 10 ml of CTAB (0.2 M), 120 l of AgNO3 (0.1 M), and 600 l of hydroquinone (0.1 M) were mixed together as growth solution. When the color of the growth solution turned from yellow to colorless, 320 l of seed solution was added. The desired longitudinal surface plasmon resonance peak was obtained after keeping the reaction mixture undisturbed in dark at 30C for 12 hours. The products were then gathered by centrifugation at 7000 RCF (relative centrifugal force) for 10 min at 30C. The supernatant was removed, and the precipitate was resuspended in 2 ml of 30C ultrapure water. Furthermore, 1 ml of the products from last step [Au (0.2 mg/ml)] was added to 10 ml of polysodium 4-styrenesulfonate (2 mg/ml) dissolved in NaCl (1 mM) solution and stirred for 1 hour at 30C. The solution was centrifuged at 7000 RCF for 10 min, and the residue was resuspended to obtain 2 ml of biocompatible polystyrene sulfonatecoated nanoparticle solution. Last, 1 ml of biocompatible polystyrene sulfonatecoated nanoparticles was added to 10 ml of -cyclodextrinPEI (2 mg/ml) dispersed in NaCl (1 mM) solution and stirred for 1 hour at 30C to obtain APC.

Apoptosis analysis at the cellular level was assessed using the Annexin Vfluorescein isothiocyanate (FITC)/propidium iodide (PI) Apoptosis Detection Kit (catalog no. E606336; Sangon Biotech Inc.). Briefly, A549 cells (3 104) cotransfected with the minicircle iterations of the FAST system and the sgRNA targeting PLK1 {pYH412 (PhCMV-p65-VP64-BldD-pA::PhCMV-BphS-P2A-YhjH-pA, 135 ng), pYH414 [PFRL-NLS-Cas9(N)-Linker-Coh2-pA, 77 ng], and pYH420 [PU6-sgRNA (PLK1)::PhCMV-DocS-Linker-Cas9(C)-NES-pA, 288 ng]} were illuminated by FRL (1 mW/cm2; 730 nm) for 4 hours once a day for 2 days and were then collected at 48 hours after the first illumination for analysis. The subsequent procedures were performed according to the manufacturers instructions and analyzed by flow cytometry (BD LSRFortessa cell analyzer; BD Biosciences). The LSRFortessa was equipped with green fluorescence channel (488-nm laser, 530/30 nm emission filter, 505 nm longpass dichroic mirror) and red fluorescence channel (561-nm laser, 610/20 nm emission filter, 595 nm longpass dichroic mirror). A gate was applied on forward scatter and side scatter to remove debris from cell populations. Data were analyzed using the FlowJo V10 software.

Total RNA of cells or tissues was extracted using the RNAiso Plus kit (catalog no. 9109; Takara Bio). A total of 500 ng of RNA was reverse transcribed into cDNA using a PrimeScript RT Reagent Kit with the genomic DNA Eraser (catalog no. RR047; Takara Bio). Quantitative PCR (qPCR) reactions were performed on the LightCycler 96 real-time PCR instrument (Roche Life Science) using the SYBR Premix Ex Taq (catalog no. RR420; Takara Bio). Program for qPCR amplifications were as follows: 95C for 10 min, followed by 40 cycles at 95C for 10 s, 60C for 15 s, and 72C for 10 s, and then 95C for 10 s, 60C for 60 s, 97C for 1 s, and last, 37C for 30 s. The qPCR primers used in this study are listed in table S4. Samples were normalized to the housekeeping gene glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as the endogenous control. Standard Ct method was used to obtain relative mRNA expression level.

Wild-type mice [8 week old, male, C57BL/6J, East China Normal University (ECNU) Laboratory Animal Center] were randomly divided into two groups. The semipermeable KrosFlo polyvinylidene fluoride hollow fiber membrane (Spectrum Laboratories Inc.; notably, the light-absorption properties of this material to lights of 300 to 1000 nm are almost the same) implants containing optogenetically engineered HEK-293 cells (pairs of 2.5-cm hollow fibers containing a total of 5 106 engineered cells) were subcutaneously implanted beneath the dorsal skin of the mice under anesthesia (two 2.5-cm hollow fibers in each mouse). At 1 hour after implantation, the mice were illuminated by FRL (10 mW/cm2; 730 nm; 2-min on, 2-min off, alternating, to avoid the thermal discomfort in mice caused by continuous illumination) for 4 hours once a day for 2 days. The control mice were kept in dark. Cells were then collected from the implanted hollow fibers at 48 hours after the first illumination, and the genomic DNA was extracted for mismatch-sensitive T7E1 assay to quantify the indel mutations of the endogenous gene CCR5.

The transgenetic Ai14 tdTomato reporter mice [6 week old, female, Gt(ROSA)26Sortm14(CAG-tdTomato)Hze, from the Jackson laboratory; Ai14 is a Cre reporter allele designed to have a loxP-flanked stop cassette, preventing the transcription of a CAG promoterdriven red fluorescent tdTomato, all inserted into the Gt(ROSA)26Sor locus] were randomly divided into three groups (vehicle, FAST without illumination, and FAST with FRL). The minicircle DNA vectors encoding the FAST system {pYH412 (PhCMV-p65-VP64-BldD-pA::PhCMV-BphS-P2A-YhjH-pA, 81 g), pYH413 [PU6-sgRNA (tdtomato stop cassette)::PhCMV-DocS-Linker-Cas9(C)-NES-pA, 173 g], and pYH414 [PFRL-NLS-Cas9(N)-Linker-Coh2-pA, 46 g]} were dissolved in Ringers solution [NaCl (8.6 g/liter), KCl (0.3 g/liter), and CaCl2 (0.28 g/liter)] and injected into mices tail vein by hydrodynamic injection. The injection volume of the DNA mixture solution was 100 l per mouse weight (gram). Twenty-four hours after injection, mice were illuminated with FRL (10 mW/cm2; 730 nm; 2-min on, 2-min off, alternating, to avoid the thermal discomfort in mice caused by continuous illumination) for 4 hours per day for 3 days (according to the time schedule in Fig. 5A). A second-round injection of the minicircle-based FAST system was performed on the fifth day, followed by 4 hours of daily illumination for three additional days. On the 15th day after the first hydrodynamic injection, mice were euthanized, and the livers were isolated for fluorescence imaging or histological analysis. The tdTomato signal from isolated liver was detected using IVIS Lumina II in vivo imaging system (PerkinElmer, USA) and frozen tissue section histological analysis.

First, dissected liver tissue blocks were soaked in 4% paraformaldehyde for 2 hours. Subsequently, the tissue blocks were stepwise dehydrated with 15% sucrose solution overnight and then soaked in 30% sucrose solution for another 3 hours. After being washed three times with PBS, freshly dissected tissue blocks (<5 mm thick) were placed on to a prelabeled tissue base mold and embedded in Tissue-Tek optimal cutting temperature (O.C.T.) compound (catalog no. 4583; Sakura). These tissue blocks were stored at 80C for freezing until ready for sectioning. The tissues were sliced into frozen sections with 5-m thickness using Cryostat Microtome (Clinical Cryostat; CM1950; Leica) for further processing or stored at 80C ultralow-temperature freezer.

A total of 5 106 of A549 cells were suspended in 0.2 ml of sterile PBS and subcutaneously injected onto the back of the 6-week-old female BALB/c nude mice (ECNU Laboratory Animal Center). When the tumor size reached about 80 to 100 mm3, APC/FAST complex containing 20 l of APC and the minicircle iteration of the FAST system {pYH412 (PhCMV-p65-VP64-BldD-pA::PhCMV-BphS-P2A-YhjH-pA, 2.7 g), pYH414 [PFRL-NLS-Cas9(N)-Linker-Coh2-pA, 1.5 g], and pYH420 [PU6-sgRNA (PLK1)::PhCMV-DocS-Linker-Cas9(C)-NES-pA, 5.8 g]} were injected intratumorally. These injected mice were randomly divided into two groups (dark and illumination). Injections were conducted under anesthesia once every 2 days for five times. Twenty-four hours after every injection, mice were illuminated with FRL (10 mW/cm2; 730 nm; 2-min on, 2-min off, alternating, to avoid the thermal discomfort in mice caused by continuous illumination) according to the time schedule in Fig. 6A or kept in dark. Mice of the vehicle control group were intratumorally injected with 20 l of APC and 50 l of PBS and were then illuminated with FRL (10 mW/cm2; 730 nm; 2-min on, 2-min off), as indicated in Fig. 6A. The tumor sizes and the body weights of mice were measured every 2 days. On the 15th day after the first intratumor injection, all mice were sacrificed and tumor weights were recorded. The tumor volumes were measured using a digital caliper and calculated by the following formula: tumor volume = [length of tumor (width of tumor)2]/2. Then, tumors were isolated for indel mutation analysis and tumor apoptosis detection by hematoxylin and eosin (H&E) staining, TUNEL, and caspase-3labeling assays.

Glass slides that hold the frozen tissue sections were washed with PBS three times for 5 min each time, transferred to 0.5% Triton X-100 (dissolved in PBS; Sigma-Aldrich) for 10 min, and washed with PBS twice for 5 min each time. The slides were rinsed in running tap water at room temperature for 1 min. The samples were then stained in hematoxylin staining solution (catalog no. E607317; Sangon Biotech Inc.) for 8 min and washed in running tap water for 10 min. Next, the samples were differentiated in 1% acid alcohol for 10 s, washed in running tap water for 30 min, and were then counterstained in eosin staining solution (catalog no. E607321; Sangon Biotech Inc.) for 30 s to 1 min and washed in running tap water for 10 min. Last, the tissue sections were sealed by a drop of mounting medium over the tissue and then covered by a coverslip. The prepared slides were then observed by a microscope (DMI8; Leica) equipped with an Olympus digital camera (Olympus DP71; Olympus).

A TUNEL Apoptosis Assay Kit (catalog no. 30063; Beyotime Biotechnology Inc.) was used to evaluate tumor tissue apoptosis according to the manufacturers instructions. After washing three times with PBS, the slides were incubated with 4,6-diamidino-2-phenylindole (DAPI) solutions (5 g/ml; catalog no. C1002; Beyotime Inc.) for 2 to 5 min at room temperature. The slides were further washed three times with PBS and mounted with the antifade mounting media. Last, the slides were sealed and observed by a fluorescence microscope (DMI8; Leica) equipped with an Olympus digital camera (Olympus DP71; Olympus). TUNEL-positive nuclei were stained green, and all other nuclei were stained blue.

Isolated tumor frozen tissue sections were thawed at room temperature for 15 min and rehydrated in PBS for 10 min. The tissue samples were surrounded with a hydrophobic barrier using a barrier pen after draining the excess PBS. Then, the slides were soaked in 0.5% Triton X-100 (dissolved in PBS; catalog no. 9002-93-1; Sigma-Aldrich) for 20 min. Nonspecific staining between the primary antibodies and the tissue samples was blocked by incubating sections in the block buffer (1% FBS in PBS) for 1 hour at room temperature. After incubating with the anticaspase-3 antibody (1:100; catalog no. ab32351; Abcam) overnight at 4C, the slides were washed three times for 15 min each time in PBS and then incubated with the Alexa Fluor 555 goat anti-rabbit immunoglobulin G antibody (1:500; catalog no. ab150078; Abcam) for 1 hour at room temperature. After washing three times with PBS, the slides were incubated with DAPI solutions (5 g/ml; catalog no. C1002; Beyotime Inc.) for 2 to 5 min at room temperature. The slides were further washed three times with PBS and mounted with the antifade mounting media. Last, the slides were sealed and observed by a fluorescence microscope (DMI8; Leica) equipped with an Olympus digital camera (Olympus DP71; Olympus). Caspase-3positive cytoplasm was stained red, and all nuclei were stained blue.

All experiments involving animals were conducted in strict adherence to the guidelines of the ECNU Animal Care and Use Committee and in direct accordance with the Ministry of Science and Technology of the Peoples Republic of China on Animal Care. The protocols were approved by the ECNU Animal Care and Use Committee (protocol IDs, m20180105 and m20190607). All mice were euthanized after the termination of the experiments.

All in vitro data represent means SD and are described separately in the figure legends. For the animal experiments, each treatment group consisted of randomly selected mice (n = 3 to 5). Comparisons between groups were performed using Students t test, and the results are expressed as means SEM. GraphPad Prism software (version 6) was used for statistical analysis.

Acknowledgments: We are grateful to all the laboratory members for cooperation in this study, especially J. Jiang, S. Zhu, and X. Yang. Funding: This work was financially supported by the grants from the National Key R&D Program of China, Synthetic Biology Research (no. 2019YFA0904500), the National Natural Science Foundation of China (NSFC; no. 31971346 and no. 31861143016), the Science and Technology Commission of Shanghai Municipality (no. 18JC1411000), the Thousand Youth Talents Plan of China, and the Fundamental Research Funds for the Central Universities to H.Y. This work was also partially supported by NSFC no. 31901023 to N.G. We also thank the ECNU Multifunctional Platform for Innovation (011) for supporting the mouse experiments and the Instruments Sharing Platform of School of Life Sciences, ECNU. Author contributions: H.Y. conceived the project. H.Y. and Y.Y. designed the experiment, analyzed the results, and wrote the manuscript. Y.Y., X.W., J.S., H.L., and Y.C. performed the experimental work. Y.P., D.L., and N.G. analyzed the results and revised the manuscript. All authors edited and approved the manuscript. Competing interests: The authors declare that they have no competing interests. Data and materials availability: All data needed to evaluate the conclusions in the paper are present in the paper and/or the Supplementary Materials. Additional data related to this paper may be requested from the authors. All genetic components related to this paper are available with a material transfer agreement and can be requested from H.Y. (hfye{at}bio.ecnu.edu.cn).

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Engineering a far-red lightactivated split-Cas9 system for remote-controlled genome editing of internal organs and tumors - Science Advances

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Molecular Probes Market 2020 Global Industry Analysis, Opportunities, Major Applications and Forecast to 2027 – Cole of Duty

Friday, July 10th, 2020

Molecular probes are the part of small RNA or DNA which recognizes the complementary sequences in DNA and RNA molecules. Molecular probes are used in identification and isolation of specific RNA or DNA sequences from organism. Molecular probes offers as the resources for various applications such as chromosomal mapping, molecular cytogenetics, and DNA fingerprinting. Also, molecular probes are used in various fields such as physiology, embryology, scientific classification, and hereditary building.

Increase in development of map-based cloning of agronomical important genes, marker based gene tags, phylogenetic analysis is expected to boost the global molecular probes market growth. Furthermore, continuous development in genetic engineering technology will have the positive impact on global molecular probes market growth. Molecular probes are developed and designed for genetic engineering research and widely used for diagnosis of infectious diseases. Moreover, increase in government initiatives for clinical investigations in molecular probes, it is expected to propel the growth of molecular probes market during this forecast period.

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However, lack of robust reimbursement framework for customized and genomic medicine is the major restraining factor which is expected to hinder the growth of global molecular probes market.

Market Key Players

Various key players are discussed in this report such as BioRad Laboratories, Hologic, Sysmex Corporation,Dako, Danaher, Thermo Fisher Scientific, and bioMerieux SA.

Market Taxonomy

By Product

By Application

By End User

By Region

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Molecular Probes Market 2020 Global Industry Analysis, Opportunities, Major Applications and Forecast to 2027 - Cole of Duty

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Israel Innovation Authority to invest almost $4 million in bio-convergence R&D programs – CTech

Friday, July 10th, 2020

The Israel Innovation Authority (IIA) will invest nearly $4 million in a new call for proposals in the field of bio-convergence. The IIA announced on Thursday that it is inviting researchers in academia, hospitals and commercial companies to submit requests for R&D funding to develop programs commercializing academic knowhow for medical innovation in bio-convergence, an approach that integrates biology with additional disciplines from engineering such as electronics, AI, physics, computer science, nanotechnology, material science, and advanced genetic engineering. The total budget for the project will be NIS 13.5 million (approximately $3.92 million)

"Given that bio-convergence is still a burgeoning technological field, most relevant expertise in the area remains concentrated in academic institutions," said Aharon Aharon, CEO of the Israel Innovation Authority. "The Israel Innovation Authoritys call for proposals will help in developing R&D programs with the potential to contribute to the commercial application of this technology. This synthesis of academia and industry is part of an overall attempt to develop an innovative ecosystem that will be an engine of growth for Israeli industry."

This is the IIAs first call for proposals from academia and industry in the field of bio-convergence in 2020, with the Israeli government's tech investment arm hoping this will pave the way for commercial deployment through two separate tracks.

In the first track, the proposal must relate to applied multidisciplinary research in medicine, joining a top researcher in the life sciences with at least one leading researcher in the field of engineering, computer sciences, math, or physics. In the second track, the proposal will be for commercialization of medical expertise, developed through multidisciplinary life sciences research integrating engineering, computer science, mathematics or physics.

The proposals must be submitted by September 21, with the results to be finalized in December 2020.

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Israel Innovation Authority to invest almost $4 million in bio-convergence R&D programs - CTech

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PM Imran orders distribution of wheat from government warehouses – The Express Tribune

Friday, July 10th, 2020

ISLAMABAD:

Prime Minister Imran Khan on Friday ordered distribution of wheat from government warehouses in Punjab to the local markets to mitigate the effects of an impending flour crisis.

The bureaucracy had advised the premier to distribute wheat stocks from government warehouses in October.

However, the premier said, You should immediately bring wheat to the market and provide it at a cheaper price by setting up markets and sale points.

The premier added that if need be, wheat would be imported in October if needed.

Earlier, on Jun 9 it was reported that Pakistan is facing a shortfall of 1.4 million tons of wheat because of a decrease in yield, a development that is set to aggravate the existing flour crisis in the coming months.

The Federal Committee on Agriculture (FCA) was informed about the impending crisis during a meeting held on Wednesday, June 9, to review the Khareef season.

The wheat production target last year was set at 27 million tonnes. This year, there is a shortfall of 1.4 million tonnes and 79.95pc of the procurement target has been achieved.

Speaking during the meeting, Federal National Food Security and Research Minister Syed Fakhar Imam stressed the need to increase wheat production.

We need a breakthrough in high-yield wheat variety through genetic engineering, he added.

Our country has the best irrigation system which is not being used properly. Wheat is grown on 36pc of the countrys cultivated area.

Food Security Commissioner Dr Waseem informed the participants of the meeting that after many years, the country had exceeded the chickpea production target of 540,000 tonnes.

This year, there will be saving of Rs87 million as there will be less chickpea import, he added.

Potato production for the current year is 4.43 million tonnes against 4.4 million tonnes recorded last year. Balochistan also recorded a bumper crop of tomato this year.

Imam said there was a need to increase the production of oil seeds (sunflower, canola, rosehip and mustard).

The Indus River System Authority representative informed the participants of the meeting that there would 9pc more water available for Khareef season this year.

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PM Imran orders distribution of wheat from government warehouses - The Express Tribune

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Genetically Modified Crops: The solution to global food insecurity – GhanaWeb

Friday, July 10th, 2020

Opinions of Thursday, 9 July 2020

Columnist: Joy Adzovie

File photo: Some GM crops

Genetically Modified Crops (GM crops) have generated a lot of controversies over the years. They have sparked debates among farmers and consumers alike with people always particularly paying attention to labelled GM and non-GM commodities on the market.

Some describe it as genetic modification. Some call it genetic engineering. Some call them genetically modified organisms (GMOs). Others describe them as biotechnology products, although biotechnology is a broader term. But all of them refer to the same thing.

A lot of ethical concerns have arisen about GM technology over the years. A very common claim made by some anti-GM activists is that you cannot play God which implies that scientists are defying the natural order of creation. Others are concerned about possible health risks associated with the consumption of GM foods although they have been proven scientifically to be safe, 20 years after their introduction.

In fact, in countries like USA, Brazil and South Africa, more than 80% of all soya beans, maize and cotton are GM crops. But there has been no single evidence of any of these crops negatively impacting the health of consumers in those countries. Before GM food is released for consumption, it is subjected to rigorous scrutiny which has zero tolerance for errors.

So, what exactly are GM crops?

In a bid to optimize yield, farmers have been breeding suitable varieties of crops through conventional selection for several centuries. This has made most wild ancestors of crops such as teosinte of maize go into extinction leaving the elite cultivars which look bigger and develop more desirable traits over the generations.

This method of breeding is known as selective breeding or artificial selection which is globally accepted but currently inefficient to feed a fast-growing population anticipated to reach 9.6 billion in the next couple of decades.

The exponential rise in population is inversely related to available land area hence the need for a more strategic approach to efficiently utilize the limited land resource to feed the growing global population. Also, pests and diseases, climate change, amidst other abiotic factors severely constrain crop production.

Biotechnology (which includes genetic modification) is an applied science that harnesses the natural biological capabilities of microbial, plants and animal cells for the benefit of mankind. It has changed the quality of life through improved medicine, diagnostics, agriculture and waste management, as well as offered opportunities for innovation and discoveries.

Genetic engineering is used to efficiently and precisely modify targeted plants using advanced biotechnological techniques. Advances in molecular biology have helped eliminate certain gaps in breeding such as reducing time to successfully introduce (introgress) a gene of interest into a commercial crop variety through a process called speed breeding and eradicating linkage drags associated with conventional breeding. The principle is a simple one.

To genetically improve or enhance a crop such as sweet potato which is susceptible to nematode attack, another crop such as tomato that is resistant to nematode attack is identified and the gene of interest is isolated. The gene isolated from the tomato is then introduced into the sweet potato. The host plant becomes a transgenic or genetically modified plant which expresses the desired trait (resistance to nematode) in subsequent generations.

Genetic engineering has had several uses such as in biofortification of crops to increase the concentration and availability of nutrients in crops hence solving hidden hunger problem faced by several African countries. The technology has also been used in the enhancement of plant architecture to optimize land usage and increase yield per area of land cultivated; and improved crops with heightened tolerance or resistance to both biotic and abiotic stresses including diseases and weather.

Benefits of GM crops

Some analysis shows that between 1996 and 2015, GM technology increased global production of corn by 357.7 million tons, soybean by 180.3 million tons, cotton fiber by 25.2 million, and canola by 10.6 million tons. GM crops also significantly reduced the use of agricultural land due to this higher productivity.

In 2015 alone, they prevented almost 20 million hectares from being used for agricultural purposes, thus reducing the environmental impact of cultivating forests or wildlands. This is a great environmental benefit derived from higher agricultural yield.

Unfortunately, in Africa, only a few countries including South Africa and South Sudan have allowed for the growing of GM crops and are enjoying from these benefits. Ghana has not allowed for the local production of GM crops although parliament passed a law in 2011 to allow for their introduction.

Genetic engineering is a viable way to eradicate hunger and ensure food security in the coming decades hence is pivotal to achieving Sustainable Development Goal (SDG) 2 on eliminating hunger. Yield losses due to changing or fluctuating climate, pests, and diseases, drought, acidic or saline soils and, heat stress can all be remedied by growing genetically modified crops. GM technology is a blessing to mankind and promises a hunger-free future especially in such unsettling times with the COVID-19 pandemic. Lets embrace it.

Joy Adzovie

Teaching and Research Assistant - University of Ghana

BSc. Agriculture- University of Ghana

GhanaWeb is not responsible for the reportage or opinions of contributors published on the website. Read our disclaimer.

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Genetically Modified Crops: The solution to global food insecurity - GhanaWeb

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PM orders to bring wheat from government warehouse to general ma – The Express Tribune

Friday, July 10th, 2020

ISLAMABAD:

Prime Minister Imran Khan on Friday ordered distribution of wheat from government warehouses in Punjab to the local markets to mitigate the effects of an impending flour crisis.

The bureaucracy had advised the premier to distribute wheat stocks from government warehouses in October.

However, the premier said, You should immediately bring wheat to the market and provide it at a cheaper price by setting up markets and sale points.

The premier added that if need be, wheat would be imported in October if needed.

Earlier, on Jun 9 it was reported that Pakistan is facing a shortfall of 1.4 million tons of wheat because of a decrease in yield, a development that is set to aggravate the existing flour crisis in the coming months.

The Federal Committee on Agriculture (FCA) was informed about the impending crisis during a meeting held on Wednesday, June 9, to review the Khareef season.

The wheat production target last year was set at 27 million tonnes. This year, there is a shortfall of 1.4 million tonnes and 79.95pc of the procurement target has been achieved.

Speaking during the meeting, Federal National Food Security and Research Minister Syed Fakhar Imam stressed the need to increase wheat production.

We need a breakthrough in high-yield wheat variety through genetic engineering, he added.

Our country has the best irrigation system which is not being used properly. Wheat is grown on 36pc of the countrys cultivated area.

Food Security Commissioner Dr Waseem informed the participants of the meeting that after many years, the country had exceeded the chickpea production target of 540,000 tonnes.

This year, there will be saving of Rs87 million as there will be less chickpea import, he added.

Potato production for the current year is 4.43 million tonnes against 4.4 million tonnes recorded last year. Balochistan also recorded a bumper crop of tomato this year.

Imam said there was a need to increase the production of oil seeds (sunflower, canola, rosehip and mustard).

The Indus River System Authority representative informed the participants of the meeting that there would 9pc more water available for Khareef season this year.

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PM orders to bring wheat from government warehouse to general ma - The Express Tribune

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Nema To Draft Biosafety Regulations And Guidelines – New Vision

Friday, July 10th, 2020

The National Environment Management Authority (NEMA) plans to draft regulations that will guide the environmental release of genetically modified organisms.

Kasese district chairman leading a team that visited Mubuku GM cassava trial garden. PHOTOS: Prossy Nandudu

The National Environment Management Authority (NEMA) plans to draft regulations that will guide the environmental release of genetically modified organisms.

Under the revised Act of 2019, NEMA was given the mandate to regulate GMOs in the environment although the regulations were not made, until the Genetic Engineering Regulatory Act (GERA) that is before parliament is passed into law to give details on the regulatory process.

This was revealed by the executive director NEMA, Dr.Tom Okurut during a meeting organised by the Science Foundation for Livelihoods and Development (SCIFODE) at a monthly media bio cafe, on NEMA Act 2019 emerging regulations and guidelines on Wednesday.

"In the absence of a specific law for GMO regulation, we should move to draft regulations and guidelines, we didn't want to go first, now that it has stayed, we cannot delay, we must start because GMOs are already with us," said Okurut.

To ensure that the process takes shape, Okurut said they're in talks stakeholders such as the Ministry of Science Technology and Innovations (MOSTI), Uganda National Council for Science and Technology (UNCST), researchers among others to secure funding for the process.

According to Okurut, the NEMA Act 1995 had omissions especially on aspects such as oil and gas industry waste, electronic waste, and management of GMOs.

He, however, adds that these have since been catered for in the amended act of 2019, apart from the aspect of GMOs that we are supposed to make laws that will regulate it. But for NEMA to make the regulations, they had to wait for the GERA bill to be passed into law, an issue which is not yielding results.

"There are still pseudo scientists peddling lies about the technology without taking time to understand the basic science used by researchers in developing these products and we need the law to regulate the use, entry, consumption of all products from GMOs," Okurut said.

Okurut was backed by the director of regulation and biosafety at the Ministry of Science Technology and Innovations, Dr.James Kasigwa who seconded NEMA to use the amended act and regulate GMOs.

"Since we don't have a dedicated law, we can make use of NEMA act to have a stop-gap, issues of GMOs are real. Kenya now plants genetically modified cotton, they are about to release cassava and our borders are porous, what is in Kenya, will find its way into Uganda. Let us leverage any provisions in NEMA to have anything workable to put in place a regulatory framework," added Kasigwa.

Dr. Kasigwa noted that MOSTI is willing to cooperate with NEMA to ensure that a regulatory framework is in place

Currently, the agriculture sector is faced with the challenge of pests and diseases and climate change which are threatening many crops like bananas devastated by the bacterial wilt, Maize production suffers from drought-related insect pests among others.

"Fortunately many of these have been addressed through biotechnology and are in research fields waiting for regulation to be availed to the farming community to improve our productivity and competitiveness," added Isaac Ongu, the executive director of Scifode.

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Nema To Draft Biosafety Regulations And Guidelines - New Vision

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Genome Editing Market Emerging Trends, Business Opportunities, Segmentation, Production Values, Supply-Demand, Brand Shares and Forecast 2020-2027 |…

Friday, July 10th, 2020

The Genome Editing market report by Reports and Data provides an extensive overview of the vital elements of the Genome Editing market and factors such as drivers, restraints, latest trends, regulatory scenario, competitive landscape, technological advancements, and others. This is the latest report covering the current COVID-19 scenario. The coronavirus pandemic has greatly affected every industry worldwide. It has brought along various changes in market conditions. The rapidly changing market scenario and the initial and future assessment of the impact are covered in the research report. The report discusses all the major aspects of the market with expert opinions on the current status, along with historical data.

Get FREE Sample Copy with TOC of the Report to understand the structure of the complete [emailprotected] https://www.reportsanddata.com/sample-enquiry-form/1052

In market segmentation by manufacturers, the report covers the following companies-

Thermo Fisher Scientific Inc., Merck KGaA, GenScript, Horizon Discovery Group Plc, Integrated DNA Technologies, Inc, Lonza, New England Biolabs and Sangamo Therapeutics, Inc.

The report also emphasizes the initiatives undertaken by the companies operating in the market including product innovation, product launches, and technological development to help their organization offer more effective products in the market. It also studies notable business events, including corporate deals, mergers and acquisitions, joint ventures, partnerships, product launches, and brand promotions.

Key Factors Explained In The Report:

Genome Editing product types, applications, geographies, and end-user industries are the key market segments that are comprised in this study. The report speculates the prospective growth of the different market segments by studying the current market standing, performance, demand, production, sales, and growth prospects existing in the market.

The segmentation included in the report is beneficial for readers to capitalize on the selection of appropriate segments for the Genome Editing sector and can help companies in deciphering the optimum business move to reach their desired business goals.

In market segmentation by types of Genome Editing , the report covers-

In market segmentation by applications of the Genome Editing , the report covers the following uses-

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Geographically, this report studies the top producers and consumers in these key regions:

North America

Europe

China

Japan

Southeast Asia

India

Objectives of the study:

Our panel of expert analysts specializing in the value chain has conducted an exhaustive, industry-wide study to offer readers accurate insights into the future of the Genome Editing market and give key market players authentic information derived via both primary and secondary sources of data collection. Additionally, the report also comprises of inputs from our consultants, which can help companies make the most of the available market opportunities. It also offers a detailed breakdown of the sales of Genome Editing and the factors that could potentially influence the growth of the industry. The information provided in this report will be able to help readers capitalize on the available growth prospects.

The Genome Editing market research covers a detailed analysis of the following data:

BROWSE THE COMPLETE REPORT AND TABLE OF [emailprotected] https://www.reportsanddata.com/report-detail/genome-editing-market

Key Questions Answered:

Inconclusion, the Genome Editing Market report is a reliable source for accessing the Market data that will exponentially accelerate your business. The report provides the principal locale, economic scenarios with the item value, benefit, supply, limit, generation, request, Market development rate, and figure and so on. Besides, the report presents a new task SWOT analysis, speculation attainability investigation, and venture return investigation.

David is an Experience Business writer who regularly contribute to the blog, He specializes in manufacturing news

Tags: Genome Editing IndustryGenome Editing MarketGenome Editing Market 2020Genome Editing Market forecastGenome Editing Market growthGenome Editing Market shareGenome Editing Market sizeGenome Editing Market trend

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Genome Editing Market Emerging Trends, Business Opportunities, Segmentation, Production Values, Supply-Demand, Brand Shares and Forecast 2020-2027 |...

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Brain Benefits of Exercise Can Be Gained with a Single Protein – UCSF News Services

Thursday, July 9th, 2020

A little-studied liver protein may be responsible for the well-known benefits of exercise on the aging brain, according to a new study in mice by scientists in the UC San Francisco Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research.

The findings could lead to new therapies to confer the neuroprotective effects of physical activity on people who are unable to exercise due to physical limitations.

Exercise is one of the best-studied and most powerful ways of protecting the brain from age-related cognitive decline and has been shown to improve cognition in individuals at risk of neurodegenerative disease such as Alzheimers disease and frontotemporal dementia even those with rare gene variants that inevitably lead to dementia.

But many older adults are not able to exercise regularly due to physical limitations or disabilities, and researchers have long searched for therapies that could confer some of the same neurological benefits in people with low physical activity levels.

The new study, published July 9, 2020, in Science, showed that after mice exercise, their livers secrete a protein called Gpld1 into the blood. Levels of this protein in the blood correspond to improved cognitive function in aged mice, and a collaboration with the UCSF Memory and Aging Center found that the enzyme is also elevated in the blood of elderly humans who exercise regularly. But the researchers showed that simply increasing the amount of Gpld1 produced by the mouse liver could confer many of the same brain benefits as regular exercise.

If there were a drug that produced the same brain benefits as exercise, everyone would be taking it. Now our study suggests that at least some of these benefits might one day be available in pill form, said study senior author Saul Villeda, PhD, a UCSF assistant professor in the departments of Anatomy and of Physical Therapy and Rehabilitation Science.

Villedas lab has previously shown that biological factors present in the blood of young mice can rejuvenate the aging mouse brain, and conversely, factors in the blood of older mice can bring on premature age-related cognitive decline in young mice.

These previous results led Villeda lab graduate student Alana Horowitz and postdoctoral researcher Xuelai Fan, PhD, to pursue blood-borne factors that might also confer the benefits of exercise, which is also known to rejuvenate the aging brain in a similar fashion to what was seen in the labs young blood experiments.

Horowitz and Fan took blood from aged mice who had exercised regularly for seven weeks and administered it to sedentary aged mice. They found that four weeks of this treatment produced dramatic improvements in learning and memory in the older mice, similar to what was seen in the mice who had exercised regularly. When they examined the animals brains, they found evidence of enhanced production of new neurons in the region known as the hippocampus, a well-documented proxy for the rejuvenating benefits of exercise.

To discover what specific biological factors in the blood might be behind these effects, Horowitz, Fan and colleagues measured the amounts of different soluble proteins in the blood of active versus sedentary mice. They identified 30 candidate proteins, 19 of which, to their surprise, were predominantly derived from the liver and many of which had previously been linked to functions in controlling the bodys metabolism. Two of these proteins Gpld1 and Pon1 stood out as particularly important for metabolic processes, and the researchers chose to study Gpld1 in more detail because few previous studies had investigated its function.

We figured that if the protein had already been investigated thoroughly, someone would have stumbled upon this effect, Villeda said. I like to say if youre going to take a risk by exploring something new, you might as well go big!

The team found that Gpld1 increases in the blood circulation of mice following exercise, and that Gpld1 levels correlate closely with improvements in the animals cognitive performance. Analysis of human data collected as part of the UCSF Memory and Aging Centers Hillblom Aging Network study showed that Gpld1 is also elevated in the blood of healthy, active elderly adults compared to less active elders.

If there were a drug that produced the same brain benefits as exercise, everyone would be taking it. Now our study suggests that at least some of these benefits might one day be available in pill form.

Saul Villeda, PhD

To test whether Gpld1 itself could drive the observed benefits of exercise, the researchers used genetic engineering to coax the livers of aged mice to overproduce Gpld1, then measured the animals performance in multiple tests that measure various aspects of cognition and memory. To their amazement, three weeks of the treatment produced effects similar to six weeks of regular exercise, paired with dramatic increases in new neuron growth in the hippocampus.

To be honest, I didnt expect to succeed in finding a single molecule that could account for so much of the benefits of exercise on the brain. It seemed more likely that exercise would exert many small, subtle effects that add up to a large benefit, but which would be hard to isolate. Villeda said. When I saw these data, I was completely floored.

Through this protein, the liver is responding to physical activity and telling the old brain to get young, Villeda added. This is a remarkable example of liver-to-brain communication that, to the best of our knowledge, no one knew existed. It makes me wonder what else we have been missing in neuroscience by largely ignoring the dramatic effects other organs might have on the brain, and vice versa.

Further laboratory experiments have shown that Gpld1 produced by the liver does not pass through the so-called blood-brain barrier, which protects the brain from toxic or infectious agents in the blood. Instead, the protein appears to exert its effects on the brain via pathways that reduce inflammation and blood coagulation throughout the body. Both blood coagulation and inflammation are known to be elevated with age and have been linked to dementia and age-related cognitive decline.

The lab is now working to better understand precisely how Gpld1 interacts with other biochemical signaling systems to produce its brain-boosting effects, in hopes of identifying specific targets for therapeutics that could one day confer many of the protective benefits of exercise for the aging brain.

Authors: Additional authors on the study were Gregor Bieri, Lucas Smith, Cesar Sanchez-Diaz, Adam Schroer, and Geraldine Gontier of the UCSF Department of Anatomy; Kaitlin Casaletto and Joel Kramer of the UCSF Memory and Aging Center; and Katherine E. Williams of the UCSF Sandler-Moore Mass Spectrometry Core Facility.

Funding: The research was funded by Hillblom Foundation predoctoral and postdoctoral fellowships, Irene Diamond AFAR postdoctoral fellowship, the National Institutes of Health (NIH) National Institute on Aging (NIA) (AG064823, AG058752, AG023501, AG053382, AG055797), and a gift from Marc and Lynne Benioff.

Disclosures: The authors declare no conflict of interest. Horowitz, Fan, and Villeda are named as inventors on a patent application arising from this work.

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Business Market Insights Launches Affordable Subscription Plans to Serve the Increasing Demand for Overall Genome Editing Market Research – Jewish…

Thursday, July 9th, 2020

The Europe genome editing market on the basis of application is segmented into genetic engineering, cell line engineering and others. The cell line engineering segment is anticipated to grow at a CAGR of 17.5% during the forecast period. Moreover, the genetic engineering segment is expected to grow at the significant rate during the coming years owing to its sub segments such as animal genetic engineering and plant genetic engineering that are being carried out extensively.

Rising demand for aftermarket automotive parts is fueling the growth of the Genome Editing market. Moreover, the increase in the adoption of electric vehicles is anticipated to boost Genome Editing market growth in the forecast period. The aftermarket or replacement market plays an important role in Genome Editing market. With the increasing awareness of preventive maintenance as well as scheduled servicing of vehicles, consumers today are focusing on maximizing the lifespan value of their existing vehicles. This has significantly bolstered the growth of aftermarket parts and services demand and has generated new revenue opportunities for an extensive number of players operating in the automotive aftermarket industry.

Biotechnology is wide industry which is comprised of the enormous group of application that has enabled researchers and scientists to evolve the healthcare services and facilities for the humans, animals and plants. The wide range of application has also helped most of the industries to introduce the biotechnological products for commercialization and has generated so much of revenue and innovated novel products that have benefited the producers and consumers. The major market is contributed through the genome editing and the technologies have enabled to diagnosed and treat various chronic diseases.

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Gene therapy innovations: Sarepta and Codiak partner on exosomes – Pharmaceutical Technology

Thursday, July 9th, 2020

Exosomes could be used to improve precision medicine approaches in various disease areas. Credit: Shutterstock.

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Genetic medicine-focused Sarepta Therapeutics has signed a two-year research agreement with Codiak Biosciences in which they will develop engineered exosome-derived therapeutics for neuromuscular diseases with few or no treatment options.

The collaboration will leverage Codiaks exosomeengineering and manufacturing capabilities with Sareptas expertise in precision genetic medicineto develop next generationtherapeutics, states Sarepta spokesperson Tracy Sorrentino.

According to the terms of the agreement, Sarepta has the exclusive option to license five targets of interest that are identified as a result of using Codiaks proprietary exosome-focused engEx platform. In return, Codiak is eligible for up to $72.5m in upfront and near-term license payments, plus research funding.

Exosomes are essential to the intercellular communication system that facilitates the transfer of many molecular payloads between cells. They have a few benefits linked to them being endogenous and inherently nonimmunogenic, as Codiak spokesperson Kate Niazi-Sai explains.

Founded five years ago, Codiaks mission is to make precision exosome therapeutics a reality by solving engineering and manufacturing challenges to enable exosomes to deliver precise therapeutics in a targeted way, notes Niazi-Sai. To this end, the company developed its engEx platform.

Using this platform, Codiak can design exosomes with precisely engineered properties, incorporate various types of biologically active molecules and direct them to specific cell types and tissues, says Niazi-Sai.

Sarepta and Codiak are hopeful that exosomes will help overcome some general issues facing adeno-associated virus (AAV)-based gene therapies. Sorrentino notes: The agreement with Codiak is part of our broader strategy to build an enduring model by exploring non-viral delivery options and next-generation genetic medicines.

Exosomes being a non-viral targeteddelivery approach that is inherently non-immunogenic means they might open up avenues for more targeted deliveryand potential re-dosing, Sorrentino notes. Niazi-Sai agrees with this sentiment.

AAVs have some limitations namely they are one-time therapies with current approaches, adds Sorrentino. They cannot be re-dosed due to the post-administration development of neutralising antibodies (NAbs) where the body identifies the virus as foreign and begins to mount an attack, which can diminish the effectiveness of a gene therapy or cause side effects.

There is a significant need to identify non-viral delivery vehicles for rare disease, specifically in neuromuscular conditions where therapeutic doses are high, explains Niazi-Sai.

To solve this problem, exosomes have a unique tropism compared to other delivery systems, and we can alter the tropism by engineering the exosome surface, with the goal of specifically reaching diseases of the muscle, says Niazi-Sai. Sorrentino explains that tropism is the ability to guide a specific cargo to the cell of interest.

Neuromuscular diseases also make particular sense for this partnership since this is an area of expertise for Sarepta. The company has focused on Duchenne muscular dystrophy (DMD) and other limb-girdle muscular dystrophies (LGMD) for a long time; both of Sareptas approved products Vyondys and Exondys are for DMD.

This research agreement with Codiak represents Sareptas third deal in 2020. One of the other agreements is a research partnership with Selecta Biosciences to leverage its immune tolerance platform in DMD and LGMD, which may allow re-dosing of patients on gene therapy.

The other is a collaboration to develop next-generation AAV vectors for muscle diseases with Dyno Therapeutic, a company that focuses on using artificial intelligence and machine learning to improve gene therapy vectors.

These deals all play into Sareptas broader strategy to collaborate with leaders in their respective fields in an effort to help advance the science, providethe greatest benefit to more patients, improve the utility and benefit of gene-based therapies, and ultimately deliver on our mission to use precision medicine to transform the lives of people with rare diseases, explains Sorrentino.

Sorrentino adds: We recognise helping patients is a team approach, and achieving our mission often means bringing together the science, people and advocates with a shared mission and specific expertise.

In fact, Sarepta has now signed a fourth deal with Hansa Biopharma, a leader in immunomodulatory enzyme technology in rare immunoglobulin G mediated disease, which has developed imlifidase. Under the terms of the agreement, Sarepta will develop and promote imlifidase as a pre-treatment to its gene therapy administration in DMD and LGMD to allow more patients to be eligible for this precision medicine approach.

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Search for cure for common parasitic infection focus of $5.5 million NIH grant – Washington University School of Medicine in St. Louis

Thursday, July 9th, 2020

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Toxoplasma infection affects about 2 billion people globally

Parasitologist L. David Sibley, PhD (standing), the Alan A. and Edith L. Wolff Distinguished Professor of Molecular Microbiology at Washington University School of Medicine in St. Louis, talks with postdoctoral researcher Alex Rozenberg, PhD, (left) and staff scientist Joshua Radke, MD. The three are part of an international effort led by Sibley to find drugs to cure toxoplasmosis, a parasitic disease characterized by vision problems and brain complications.

L. David Sibley, PhD, the Alan A. and Edith L. Wolff Distinguished Professor of Molecular Microbiology at Washington University School of Medicine in St. Louis, has spent decades unraveling the secrets of Toxoplasma gondii, a parasite spread by cats and contaminated water and food. People infected with Toxoplasma can generally control the infection, but the parasite remains in their bodies for life and can reactivate to cause toxoplasmosis, a disease characterized by vision problems and life-threatening complications in the brain.

Sibleys discoveries have put him at the forefront of the field of parasite biology. A few years ago, he was busy fielding interview requests from journalists about his latest high-profile paper when he opened an email from a woman in Heidelberg, Germany.

I would like to ask you, wrote the woman, after explaining that her husband was dying of toxoplasmosis, how far (near?) is the possibility of human therapy based on your work?

To Sibley, the email was a wake-up call.

We always say that we do basic science so that one day there might be an improvement in human health, but we dont always push hard enough to convert our discoveries into benefits for patients, Sibley said. After thinking hard about this issue, my colleagues and I came up with the idea of trying to find chemical compounds that eliminate the chronic stages of the parasite, rather than just control it, like current drug therapies do. We know a lot about the biology of this parasite. My lab has spent 30 years figuring out all the tricks the parasite uses to block the immune system. We have developed sophisticated genetic tools and animal models to monitor infection. All this has led to a pile of high-profile papers, and recognition, but has not really had an impact on people who suffer from this infection. I thought, Why not see if we can identify small molecules that might lead to a curative drug?

That plaintive email eventually led Sibley and colleagues at the California Institute for Biomedical Research (Calibr) in La Jolla, Calif.; the Broad Institute in Cambridge, Mass.; and the International Centre for Genetic Engineering and Biotechnology in New Delhi, India to launch an effort to identify chemical compounds that eliminate the chronic stages of Toxoplasma and have the potential to be developed into drugs to eradicate the infection. As principal investigator, Sibley has received a $5.5 million grant from the National Institute of Allergy and Infectious Diseases of the National Institutes of Health (NIH) to support the research.

Toxoplasma is a parasite that naturally cycles between mice and cats. An infected cat excretes millions of the parasite in its feces in a form known as oocysts, contaminating the soil and water. A mouse gets infected by eating food such as fruit or seeds contaminated with oocysts, and a cat eats the mouse, completing the cycle.

Humans and other animals are accidental participants in this process. Herbivorous animals like cows and sheep can become infected as they graze. People become infected by eating undercooked meat from such animals or unwashed vegetables, or by drinking contaminated water. Some people become infected by failing to wash their hands after cleaning cats litter boxes. Once inside a persons digestive tract, the parasite emerges from the cyst, burrows through the intestinal wall and spreads to the muscle, heart, brain and eyes. There, it develops into a cyst form and remains for the rest of the persons life.

About a quarter of the worlds population is thought to be infected with Toxoplasma. Most people do not have symptoms because a healthy immune system keeps the parasite in check. In people with compromised immune systems, though, the parasites do not stay in their cysts and instead begin to multiply, causing debilitating, sometimes fatal, damage to the brain, eyes and other organs. Women who become infected during pregnancy may pass the infection to their fetuses, resulting in severe birth defects.

Drugs for toxoplasmosis only target the parasite in the active phase, leaving cysts untouched. Since parasites may emerge from the cysts at unpredictable times, people must continue taking the drugs for prolonged periods, sometimes more than a year. Even so, the risk of relapse is high. Supplementing current therapies with a drug that eliminates the cysts not only would speed up treatment, it would cure the infection.

Nobodys ever really looked for drugs that target the latent, cyst phase, Sibley said. You cant just take drugs that work against other microbial infections and repurpose them. Thats been tried and it doesnt work very well. Its hard to kill the cyst form. Thats why they form cysts: to protect themselves when they are in an inhospitable environment. Were going to have to really dig into the biology and thats difficult and takes time. Since the potential monetary payoff will likely be small, big pharma just isnt interested. If potential drugs are going to be found, they will have to be started by academic labs.

The research project is already underway. A group led by Stuart Schreiber, PhD, a chemical biologist at the Broad Institute, screened some 80,000 small molecules for their ability to inhibit parasite growth and identified several promising leads. A group of structural biologists at the International Centre for Genetic Engineering and Biotechnology led by Amit Sharma, PhD, is analyzing how the initial leads interact with their target enzyme. A detailed understanding of the molecular structure will inform efforts to optimize the compounds. Medicinal chemist Arnab Kumar Chatterjee, PhD, leads a group at Calibr that is creating new molecules based on the promising leads but with improved potency, safety, bioavailability and other features. And Sibleys lab at the School of Medicine is responsible for the biological testing, making sure the team stays focused on compounds that actually have the capacity to treat the cyst stage.

The compounds weve started working on may not ultimately lead to a drug that works, Sibley said. There are no guarantees in this kind of work. But I think what we can do is establish a path forward. We can identify appropriate targets, establish the potency, and define the safety profile that youd need for an effective clinical candidate. Then, maybe more people will pick up on our leads and do the very difficult work that is necessary to get drug candidates evaluated in humans and get one of those candidates approved as a medicine, so people dont have to suffer and die from this devastating illness.

Washington University School of Medicines 1,500 faculty physicians also are the medical staff of Barnes-Jewish and St. Louis Childrens hospitals. The School of Medicine is a leader in medical research, teaching and patient care, ranking among the top 10 medical schools in the nation by U.S. News & World Report. Through its affiliations with Barnes-Jewish and St. Louis Childrens hospitals, the School of Medicine is linked to BJC HealthCare.

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Ziopharm Oncology Announces Initiation of Phase 1 Trial Evaluating Rapid Personalized Manufacturing CAR-T Technology in Patients with Relapsed CD19+…

Thursday, July 9th, 2020

BOSTON, July 09, 2020 (GLOBE NEWSWIRE) -- Ziopharm Oncology, Inc. (Ziopharm or the Company) (Nasdaq:ZIOP), today announced the initiation of a phase 1 clinical trial to evaluate CD19-specific CAR-T, using its Rapid Personalized Manufacturing (RPM) technology, as an investigational treatment for patients with relapsed CD19+ leukemias and lymphomas. The trial is now open for enrollment at The University of Texas MD Anderson Cancer Center.

In this trial, the Company utilizes its non-viral Sleeping Beauty genetic engineering technology to infuse CAR-T the day after electroporation. Ziopharms RPM CD19-specific CAR-T therapy results from the stable, non-viral insertion of DNA into the genome of resting T cells to co-express the chimeric antigen receptor (CAR), membrane-bound IL-15 (mbIL15) and a safety switch.

We are pleased to expand the scope of our clinical development with MD Anderson, as we seek to evaluate our RPM technology using CD19-specific CAR-T cells, said Laurence Cooper, M.D., Ph.D., Chief Executive Officer of Ziopharm. RPM is a promising manufacturing solution, as T cells from the bloodstream are genetically reprogramed with DNA plasmids from the Sleeping Beauty system and then simply administered the next day.

Our CAR-T therapy can be administered at low cell doses, which may control cytokine release syndrome and is appealing for the treatment of patients including those with CD19-expressing malignancies that have relapsed after allogeneic bone marrow transplantation (BMT). There are limited effective treatment options for such patients as evidenced by the low rate of remission and poor long-term survival, Dr. Cooper added.

Up to 24 patients with advanced CD19+ leukemias and lymphomas who have relapsed after allogeneic BMT will be enrolled in this investigator-initiated trial (NCT03579888). The primary endpoint of the study is to determine the safety and maximum tolerated dose of donor-derived genetically modified CD19-specific T cells manufactured using the RPM process. An additional study is planned through Ziopharms joint venture with Eden BioCell to evaluate the RPM technology using patient-derived (autologous) CD19-specific CAR-T in Greater China.

Research reveals three-year survival for adults with CD19+ acute lymphoblastic leukemia after allogeneic BMT ranges from 30% to 65%.1 For patients with other CD19+ cancers, allogeneic BMT can provide three-year survival rates between 30% to 75%.1 Few patients experience a durable remission following allogeneic BMT, regardless of the treatment modality, with some having a median survival of only 2 to 3 months.2

About Ziopharm Oncology, Inc.Ziopharm is developing non-viral and cytokine-driven cell and gene therapies that weaponize the bodys immune system to treat the millions of people globally diagnosed with a solid tumor each year. With its multiplatform approach, Ziopharm is at the forefront of immuno-oncology with a goal to treat any type of solid tumor. Ziopharms pipeline is built for commercially scalable, cost effective T-cell receptor T-cell therapies based on its non-viral Sleeping Beauty gene transfer platform, a precisely controlled IL-12 gene therapy, and rapidly manufactured Sleeping Beauty-enabled CD19-specific CAR-T program. The Company has clinical and strategic collaborations with the National Cancer Institute, The University of Texas MD Anderson Cancer Center and Regeneron Pharmaceuticals. For more information, please visit http://www.ziopharm.com.

Forward-Looking Statements DisclaimerThis press release contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts, and in some cases can be identified by terms such as "may," "will," "could," "expects," "plans," "anticipates," and "believes." These statements include, but are not limited to, statements regarding the progress, design and timing of the Company's research and development programs, the potential benefits of the Companys therapies, and the Companys expectations regarding the number of patients in its clinical trials. Although Ziopharms management team believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Ziopharm, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, changes in our operating plans that may impact our cash expenditures, the uncertainties inherent in research and development, future clinical data and analysis, including whether any of Ziopharms product candidates will advance further in the preclinical research or clinical trial process, including receiving clearance from the U.S. Food and Drug Administration or equivalent foreign regulatory agencies to conduct clinical trials and whether and when, if at all, they will receive final approval from the U.S. FDA or equivalent foreign regulatory agencies and for which indication; the strength and enforceability of Ziopharms intellectual property rights; competition from other pharmaceutical and biotechnology companies as well as risk factors discussed or identified in the public filings with the Securities and Exchange Commission made by Ziopharm, including those risks and uncertainties listed in Ziopharms Quarterly Report on Form 10-Q filed by Ziopharm with the Securities and Exchange Commission. We are providing this information as of the date of this press release, and Ziopharm does not undertake any obligation to update or revise the information contained in this press release whether as a result of new information, future events or any other reason.

Investor Relations Contacts:Ziopharm Oncology:Chris TaylorVP, Investor Relations and Corporate CommunicationsT: 617.502.1881E: ctaylor@ziopharm.com

LifeSci Advisors:Mike MoyerManaging DirectorT: 617.308.4306E: mmoyer@lifesciadvisors.com

Media Relations Contact:LifeSci Communications:Patrick BurseyT: 646.876.4932E: pbursey@lifescicomms.com

1 D'Souza A, Fretham C. Current Uses and Outcomes of Hematopoietic Cell Transplantation (HCT): CIBMTR Summary Slides, 2018. Available at https://www.cibmtr.org

2 Keil F, Prinz E, Kalhs P, et al. Treatment of leukemic relapse after allogeneic stem cell transplantation with cytotoreductive chemotherapy and/or immunotherapy or second transplants. Leukemia 2001; 15:355-361.

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Joy Adzovie: Genetically Modified Crops is the solution to global food insecurity – Myjoyonline.com

Thursday, July 9th, 2020

Genetically Modified Crops (GM crops) have generated a lot of controversies over the years. They have sparked debates among farmers and consumers alike with people always particularly paying attention to labeled GM and non-GM commodities on the market.

Some describe is as genetic modification. Some call it genetic engineering. Some call them genetically modified organisms (GMOs). Others describe them as biotechnology products, although biotechnology is a broader term. But all of them refer to the same thing.

A lot of ethical concerns have arisen about GM technology over the years. A very common claim made by some anti-GM activists is that you cannot play God which implies that scientists are defying the natural order of creation. Others are concerned about possible health risks associated with the consumption of GM foods although they have been proven scientifically to be safe, 20 years after their introduction.

In fact, in countries like USA, Brazil and South Africa, more than 80% of all soya beans, maize and cotton are GM crops. But there has been no single evidence of any of these crops negatively impacting the health of consumers in those countries. Before GM food is released for consumption, it is subjected to rigorous scrutiny which has zero tolerance for errors.

So, what exactly are GM crops?

In a bid to optimize yield, farmers have been breeding suitable varieties of crops through conventional selection for several centuries. This has made most wild ancestors of crops such as teosinte of maize go into extinction leaving the elite cultivars which look bigger and develop more desirable traits over the generations. This method of breeding is known as selective breeding or artificial selection which is globally accepted but currently inefficient to feed a fast-growing population anticipated to reach 9.6 billion in the next couple of decades. The exponential rise in population is inversely related to available land area hence the need for a more strategic approach to efficiently utilize the limited land resource to feed the growing global population. Also, pests and diseases, climate change, amidst other abiotic factors severely constrain crop production.

Biotechnology (which includes genetic modification) is an applied science that harnesses the natural biological capabilities of microbial, plants and animal cells for the benefit of mankind. It has changed the quality of life through improved medicine, diagnostics, agriculture and waste management, as well as offered opportunities for innovation and discoveries.

Genetic engineering is used to efficiently and precisely modify targeted plants using advanced biotechnological techniques. Advances in molecular biology have helped eliminate certain gaps in breeding such as reducing time to successfully introduce (introgress) a gene of interest into a commercial crop variety through a process called speed breeding and eradicating linkage drags associated with conventional breeding.

The principle is a simple one. To genetically improve or enhance a crop such as sweet potato which is susceptible to nematode attack, another crop such as tomato that is resistant to nematode attack is identified and the gene of interest is isolated. The gene isolated from the tomato is then introduced into the sweet potato. The host plant becomes a transgenic or genetically modified plant which expresses the desired trait (resistance to nematode) in subsequent generations.

Genetic engineering has had several uses such as in biofortification of crops to increase the concentration and availability of nutrients in crops hence solving hidden hunger problem faced by several African countries. The technology has also been used in the enhancement of plant architecture to optimize land usage and increase yield per area of land cultivated; and improved crops with heightened tolerance or resistance to both biotic and abiotic stresses including diseases and weather.

Benefits of GM crops

Some analysis shows that between 1996 and 2015,GM technology increased global production of corn by 357.7 million tons, soybean by 180.3 million tons, cotton fiber by 25.2 million, and canola by 10.6 million tons. GM crops also significantly reduced the use of agricultural land due to this higher productivity. In 2015 alone, they prevented almost 20 million hectares from being used for agricultural purposes, thus reducing the environmental impact of cultivating forests or wild lands. This is a great environmental benefit derived from higher agricultural yield.

Unfortunately, in Africa, only a few countries including South Africa and South Sudan have allowed for the growing of GM crops and are enjoying from these benefits. Ghana has not allowed for the local production of GM crops although parliament passed a law in 2011 to allow for their introduction.

Genetic engineering is a viable way to eradicate hunger and ensure food security in the coming decades hence is pivotal to achieving Sustainable Development Goal (SDG) 2 on eliminating hunger. Yield losses due to changing or fluctuating climate, pests, and diseases, drought, acidic or saline soils and, heat stress can all be remedied by growing genetically modified crops. GM technology is a blessing to mankind and promises a hunger-free future especially in such unsettling times with the COVID-19 pandemic. Lets embrace it.

The author is a Teaching Assistant at the University of Ghana, Graduate, Faculty of Agriculture.

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Joy Adzovie: Genetically Modified Crops is the solution to global food insecurity - Myjoyonline.com

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Genetically Modified Crops: The Solution To Global Food Insecurity – Modern Ghana

Thursday, July 9th, 2020

Genetically Modified Crops (GM crops) have generated a lot of controversies over the years. They have sparked debates among farmers and consumers alike with people always particularly paying attention to labeled GM and non-GM commodities on the market.

Some describe it as genetic modification. Some call it genetic engineering. Some call them genetically modified organisms (GMOs). Others describe them as biotechnology products, although biotechnology is a broader term. But all of them refer to the same thing.

A lot of ethical concerns have arisen about GM technology over the years. A very common claim made by some anti-GM activists is that you cannot play God which implies that scientists are defying the natural order of creation. Others are concerned about possible health risks associated with the consumption of GM foods although they have been proven scientifically to be safe, 20 years after their introduction.

In fact, in countries like the USA, Brazil, and South Africa, more than 80% of all soya beans, maize and cotton are GM crops. But there has been no single evidence of any of these crops negatively impacting the health of consumers in those countries. Before GM food is released for consumption, it is subjected to rigorous scrutiny which has zero tolerance for errors.

So, what exactly are GM crops?

In a bid to optimize yield, farmers have been breeding suitable varieties of crops through conventional selection for several centuries. This has made most wild ancestors of crops such as teosinte of maize go into extinction leaving the elite cultivars which look bigger and develop more desirable traits over the generations. This method of breeding is known as selective breeding or artificial selection which is globally accepted but currently inefficient to feed a fast-growing population anticipated to reach 9.6 billion in the next couple of decades. The exponential rise in population is inversely related to available land area hence the need for a more strategic approach to efficiently utilize the limited land resource to feed the growing global population. Also, pests and diseases, climate change, amidst other abiotic factors severely constrain crop production.

Biotechnology (which includes genetic modification) is an applied science that harnesses the natural biological capabilities of microbial, plants and animal cells for the benefit of mankind. It has changed the quality of life through improved medicine, diagnostics, agriculture and waste management, as well as offered opportunities for innovation and discoveries.

Genetic engineering is used to efficiently and precisely modify targeted plants using advanced biotechnological techniques. Advances in molecular biology have helped eliminate certain gaps in breeding such as reducing time to successfully introduce (introgress) a gene of interest into a commercial crop variety through a process called speed breeding and eradicating linkage drags associated with conventional breeding.

The principle is a simple one. To genetically improve or enhance a crop such as sweet potato which is susceptible to nematode attack, another crop such as tomato that is resistant to nematode attack is identified and the gene of interest is isolated. The gene isolated from the tomato is then introduced into the sweet potato. The host plant becomes a transgenic or genetically modified plant which expresses the desired trait (resistance to nematode) in subsequent generations.

Genetic engineering has had several uses such as in biofortification of crops to increase the concentration and availability of nutrients in crops hence solving hidden hunger problem faced by several African countries. The technology has also been used in the enhancement of plant architecture to optimize land usage and increase yield per area of land cultivated; and improved crops with heightened tolerance or resistance to both biotic and abiotic stresses including diseases and weather.

Benefits of GM crops

Some analysis shows that between 1996 and 2015, GM technology increased global production of corn by 357.7 million tons, soybean by 180.3 million tons, cotton fiber by 25.2 million, and canola by 10.6 million tons. GM crops also significantly reduced the use of agricultural land due to this higher productivity.

In 2015 alone, they prevented almost 20 million hectares from being used for agricultural purposes, thus reducing the environmental impact of cultivating forests or wildlands. This is a great environmental benefit derived from higher agricultural yield.

Unfortunately, in Africa, only a few countries including South Africa and South Sudan have allowed for the growth of GM crops and are enjoying these benefits. Ghana has not allowed for the local production of GM crops although parliament passed a law in 2011 to allow for their introduction.

Genetic engineering is a viable way to eradicate hunger and ensure food security in the coming decades hence is pivotal to achieving Sustainable Development Goal (SDG) 2 on eliminating hunger. Yield losses due to changing or fluctuating climate, pests, and diseases, drought, acidic or saline soils and, heat stress can all be remedied by growing genetically modified crops. GM technology is a blessing to mankind and promises a hunger-free future especially in such unsettling times with the COVID-19 pandemic. Lets embrace it.

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Genetically Modified Crops: The Solution To Global Food Insecurity - Modern Ghana

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LA’s ‘Wet Markets’ Could Be On The Chopping Block – LAist

Thursday, July 9th, 2020

A cashier at L.A. Fresh Poultry weighs some chicken. (Chava Sanchez/LAist)

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Zoila Isabel Sandoval sits on a hard, wooden chair in front of the spice rack at L.A. Fresh Poultry, waiting to place her order with a clerk. The basket of her rolling walker is piled with groceries. She's in a good mood. Today is her son's 40th birthday and they're going to celebrate with a big family lunch. She plans to make several Guatemalan-style dishes, including arroz con pollo chapina and pollo en jocon, a tomatillo-based stew. To do that, she needs six freshly slaughtered chickens.

Sandoval grew up in the farm town of San Rafael Las Flores in southern Guatemala, where she and her mother raised chickens and pigs at home.

"I liked seeing them grow, especially when they had little chicks or piglets," Sandoval says in Spanish.

After moving to Los Angeles two decades ago, she struggled to find a place where she could buy freshly slaughtered chickens.

"I have been eating like this ever since I was in my mother's womb," she says with a laugh.

When she discovered L.A. Fresh Poultry, a 2,000-square-foot market not far from her MacArthur Park apartment, she felt a sense of relief.

The store sells live chickens, turkeys, quails, ducks, squabs and rabbits, which its butchers will slaughter on site. In the eyes of the law, this will probably make L.A. Fresh Poultry a "wet market" a business that may soon be forbidden in the city of Los Angeles.

On June 10, the Los Angeles City Council passed a motion that could signal the beginning of the end for wet markets. The motion asks the L.A. Department of City Planning, the Department of Building and Safety and the City Attorney's office to come up with "a precise definition" of "wet market" and provide recommendations about which "establishments and practices should be prohibited."

Bob Blumenfield, one of the two city councilmembers who sponsored the motion, told us the information he's requesting is not an outright wet market ban yet. Rather, it's a "report on the feasibility of such an ordinance." But, he added, "It's the first step to prohibit the sale of living creatures for human consumption in the city of Los Angeles."

Although city officials haven't provided a definition for "wet market," the state of California defines "live animal market," an equivalent term, as "a retail food market where, in the regular course of business, animals are stored alive and sold to consumers for the purpose of human consumption." A further explanation, spelled out in California Penal Code PEN 597.3, says, "'Animal' means frogs, turtles, and birds sold for the purpose of human consumption, with the exception of poultry."

L.A. city officials are still in the process of working with L.A. City Attorney Mike Feuer to write the ordinance, according to Councilmember Paul Koretz, the motion's other sponsor. "The focus is primarily on animals that have unknown implications in terms of diseases they could spread," Koretz told us, although he acknowledges there is no guarantee the ordinance would be limited to animals that are commonly tied to illnesses.

Although no wet market or butcher shop has been the source of a COVID-19 outbreak in L.A., "There may be hygienic questions in terms of how they operate, and questions of animal cruelty in terms of how [animals] are kept and slaughtered," Koretz said. He told us he has no firsthand experience shopping at wet markets in L.A.

Ren Rowland, the chairwoman of animal rights organization PawPAC, supports the motion. She told us that whether wet market animals are wild (think bullfrogs or turtles) or domestic (think chickens, ducks, rabbits), "They also endure these terrible experiences of being transported and trafficked in these different containers in cages, in trucks and planes."

"We don't advocate for any markets to close for business," Rowland said. "We just believe that we need to stop the practice of the on-site slaughter."

The city of L.A., which has approximately 4 million residents, has maybe two dozen stores that slaughter and sell animals on their premises, according to a list provided by Blumenfield's staff. Blumenfield says the list isn't exhaustive and could potentially include businesses that are not wet markets. Regardless, these businesses make up a tiny fraction of L.A.'s nearly 1,200 markets and grocery stores.

Koretz told us he doesn't know of any major food-borne illness outbreaks that began at L.A. wet markets, "but there are some people that have become sick from eating some of the more exotic foods." He added that his knowledge of cruelty issues is secondhand.

So why the motion that could put an end to wet markets? And why do it now? One word: coronavirus.

"The fact that this virus potentially started in a wet market [in China] caused us to look at ourselves in Los Angeles, and do we have these kinds of wet markets that are cruel and potentially dangerous," Blumenfield said.

No one has conclusively determined the origins of COVID-19. Many scientists believe it originated in nature in one animal species (possibly bats) then jumped to another species (such as pangolins) before wreaking havoc on humans. In one theory, that transfer happened in a seafood and animal market near Wuhan, China.

The phrase "wet market" can mean a lot of things. Most of them merely sell fresh meat, fish and other perishable food. Others, like the one near Wuhan, also sell wild animals such as bats and civets. Although scientists may never be able to pinpoint the virus's origin, that hasn't stopped politicians or conspiracy theorists or racists from making "wet market" a pejorative term and blaming people or cultures commonly associated with them for the coronavirus pandemic.

President Donald Trump has repeatedly used the term "Chinese virus" to describe the COVID-19. As hate crimes against Asian Americans continue to rise, White House press secretary Kayleigh McEnany recently defended Trump's use of the term "kung flu," saying, "It's not a discussion about Asian Americans, who the president values and prizes as citizens of this great country. It is an indictment of China for letting this virus get here."

At the start of 2020, most Americans had never heard of wet markets. A few months later, they were Public Health Enemy #1. Even Canadian Lite Rocker Bryan Adams got in on the action.

By April, the Asian Pacific Policy & Planning Council's Hate Tracker had received more than 1,400 reports of verbal abuse, assault and shunning directed at Asian Americans, or people who look Asian.

Racism triggered by the so-called wet market-coronavirus connection even trickled down to the business sector. In late January, as the coronavirus became a growing global concern, Chinese restaurants started to see a major slump in customers.

The L.A. City Council's motion to ban wet markets which only applies within the city's boundaries and not in the San Gabriel Valley, where there are about a dozen such markets won't only impact Asian Americans. It will impact Muslims, Latinos, Armenians and anyone else who prefers meat from freshly slaughtered animals.

Koretz says he understands how the motion could be seen as discriminatory, but he views that interpretation as the result of a top-down leadership problem. "My only discomfort is with President Trump unnecessarily trying to utilize the hate against anybody different," he said, adding that Trump's divisive and racist language is an "unfortunate side element to this issue."

But Koretz maintains that there's a valid reason for the motion: "We're seeing how devastating this particular virus can be. And this practice, even though it is culturally associated with certain communities, the potential diseases will not be associated with any community. This is targeted towards health."

To Zoila Sandoval, the idea of buying meat that has been slaughtered elsewhere then frozen, swathed in plastic and shipped from hundreds of miles away is hard to accept.

Two times a week since L.A. Fresh Poultry opened 14 years ago, she has made the 20-minute walk from her home on Vermont Avenue to the store. The chance to buy freshly slaughtered animals is precisely why she comes here.

"It's killed here," she says. "It's not frozen and stored for I don't know how long. It's fresh and healthier."

She's not alone. Outside of wet markets, there's plenty of demand for freshly slaughtered, non-factory-farmed, humanely killed animals, whether it's the organic steaks of Belcampo Meat Co. or the organic, air-chilled thighs of Mary's Free-Range Chicken. Never mind the urban hipsters who home-raise chickens, sometimes for food.

Aside from a giant fiberglass rooster (and his small rabbit companion) perched on the roof, L.A. Fresh Poultry is an unassuming store next to the Virgil Avenue on-ramp of the 101. Behind the counter, bills from different countries have been stuck to the wall around a sign that reads, "I love Egypt."

Painted on another wall outside the store, a colorful parade of creatures including Daffy Duck and Bugs Bunny beckons potential customers. "Why buy frozen when you can buy fresh?" reads the mural. Indeed, in addition to the foodstuffs that any such store carries, L.A. Fresh Poultry has a live animal storage room, where chickens, rabbits and quails are kept in cages.

The market has been a neighborhood staple since opening in 2006. It serves customers seven days a week, from 8:30 a.m. until 6 p.m. This is owner Abdel Salam Elhawary's second such store. The first, Al Salam Pollera in East L.A., opened nearly 40 years ago, and is still thriving. He says approximately 80% to 85% of his customers are Mexican immigrants and the rest originally come from Guatemala or El Salvador. Elhawary also has a third store, Van Nuys Live & Fresh Poultry, which he opened in 2012.

A 68-year-old Egyptian immigrant who once taught French in his home country, Elhawary came to Los Angeles in 1980 and worked in a bank for nearly a decade before getting into the grocery game.

He started his business so Muslims could have more access to halal meats. For meat to be certified halal, whoever is doing the slaughtering must follow certain rules. The animal can't be unconscious. The butcher needs to use an extremely sharp instrument to prevent snags and the prolonging of any suffering. Allah's name must be said during the slaughter. Then, the animal must be hung upside down so the blood can drain. (By way of comparison, in industrial slaughterhouses, chickens might be shackled then electrocuted to death while sheep and pigs might be gassed into unconsciousness before they're slaughtered.)

"We have a Muslim community," Elhawary says, "it's about 40,000 to 50,000 Muslims around the [Koreatown] area. Mostly, the Bangladesh people come, and the Middle Eastern and others."

Hollywood resident Haji Ceesay, 53, is one of the market's many customers. Ceesay, a Muslim who comes from The Gambia, moved to Los Angeles in 1991. Ceesay prefers to consume freshly slaughtered animals for religious and cultural reasons.

"Back home that's what we do," Ceesay says. "We buy live chicken and it's different than the frozen ones here."

Ceesay left the store that day with six chickens.

These days, Elhawary says Muslims make up about 40% of his customers. He says the rest of his clients are Angelenos who originally came from Mexico, Central America, Armenia or Korea. He's as surprised as anyone by the diversity of his clientele, but he's happy to have the customers.

After 40 years in business, Elhawary isn't upset about the provision in the ordinance that would require him to stop selling live birds, such as quail and squab. Demand is low. The provision that would require him to stop slaughtering is another matter.

If that goes into effect, "I am gonna die," Elhawary says. "All my life is doing this. It's not only my shop. It's all over. Millions of people love to eat the fresh one."

"Millions" may be a bit of an exaggeration, but it's undeniable that live animal markets fill a need for thousands of residents, most of whom, by almost any account, are immigrants and/or people of color.

Sam Sammars, an L.A. Fresh Poultry customer who lives in East L.A., says he discovered the market in 2014 and has been coming once or twice a week since then. For him, it's worth the trip. The meat here is fresher than store-bought factory meat, and the prices are good $15 to $16 for a large, freshly slaughtered chicken.

"It tastes so natural, as if you're in the farm," he said while waiting in line to place his order.

Sammars grew up on a farm in Columbus, Ohio, where there weren't many supermarkets in the area, so he got used to the taste of fresh everything fresh fruits, fresh vegetables and fresh meat. Now 35, he says conventional farming and meat production, with their pesticides, genetic engineering, hormones and antibiotics, produce food that isn't as nutritious.

He said that if markets are prohibited from selling live and freshly slaughtered animals without the law making any distinction between chickens and ducks vs. frogs, exotic birds and wild animals, "It would be very strongly devastating."

At typical grocery stores and supermarkets, most meat comes from livestock that has been raised on "factory farms" (or what the USDA calls Concentrated Animal Feeding Operations), then slaughtered at industrial slaughterhouses and transported to markets by refrigerated trucks.

"Wet markets are selling a live animal or slaughtering it in front of you. That's very different," Blumenfield says. "When animals are just brought in and killed for human consumption, it completely avoids the regulatory system."

In fact, the state of California regulates how live animal markets, custom slaughterhouses and retail poultry plants can operate. The facilities are inspected by the California Department of Food and Agriculture to make sure they abide by health and safety regulations, which are designed to prevent the inhumane treatment of animals and the spread of diseases. The L.A. County Department of Public Health, for its part, regulates the retail portion of such businesses in accordance with the California Retail Food Code.

Regardless of the oversight process, Blumenfield also points out that the motion stems from a "cruelty issue."

"The idea is: Can we stop this cruel practice in Los Angeles?" he says, referring to slaughtering of rabbits, frogs and birds on site. "A wet market is the opposite of what you would find in a humane society."

Chef Wes Avila doesn't see wet markets that way. He says he used to buy 50 to 80 chickens per week from wet markets in Chinatown when he launched Guerrilla Tacos as a food truck, in 2014.To Avila, the complaints about wet markets aren't about ethics, they're about aesthetics. They just make some people uncomfortable.

"People want to pretend that meat comes from some magic pig tree or chicken tree. That's not the way it happens. It has to come from somewhere."

According to Elhawary, the chickens at his markets come from farms in Fresno or Ramona and he makes sure all the animals he sells are healthy.

"When they have bruises from the transportation, we trim it and throw the bad parts away. We use sharp knives, and we do the chicken fast and accurately. We don't let the chicken suffer," Elhawary says.

Nevertheless, activists who support the closure of wet markets prioritize another concern the transportation process. Rowland, of PawPAC, says people who want to maximize their profits will transport as many live animals as possible in trucks or planes, which is dangerous and inhumane.

Rowland says she doesn't believe slaughtering animals in industrial slaughterhouses then transporting the meat to grocery stores is necessarily more humane, safer or healthier.

But, she says, "There are no factory farms in the city of Los Angeles and so because of that, we don't have to address that issue."

The proposal to ban wet markets in L.A. is one part of Rowland's larger goal: putting a stop to any activities that cause animals suffering or torture. She says she's starting with California but wants that message to sweep the world.

Councilman Koretz, for his part, is waiting on the report so he can decide "whether it's a practical thing to pursue."

Although the report was supposed to come out by July 10 30 days after the motion was passed it has not yet been completed. A staffer at Councilman Koretz's office said the city expects to see the report in late July or early August.

If officials want to move forward with the proposal, the City Council will have to pass another motion directing City Attorney Feuer to draft the law.

While officials wait for the city's feasibility report, Elhawary worries. If the proposed measure moves forward, he says he may organize a demonstration with his customers. He fears that if he has to stop selling freshly slaughtered poultry, his three markets will go out of business.

In the meantime, Zoila Sandoval has been watching as the workers at L.A. Fresh Poultry process her order. After she's requested her six chickens at the counter, two licensed butchers grab them from the cages that are not visible to customers. They take the birds to the killing room, where they're slaughtered, drained and plucked. Then, two more workers remove the giblets, wash the chickens and pass them through an open doorway to a clerk.

One of the shop's two butchers, Merare Nataneal, has spent 12 years honing his craft. At 66, he worries the ordinance, if passed, will put him on the unemployment line.

"This is my work, and I don't want to lose it," Nataneal says in Spanish. "It's an uncomfortable position knowing that they might want to close this type of business down."

Behind the counter, a clerk weighs, wraps and bags the freshly killed birds. After paying at the register, Sandoval leaves L.A. Fresh Poultry under the gaze of Foghorn Leghorn, six still-warm birds piled in the basket of her walker as she rolls down Virgil Ave, heading home to make lunch for her son.

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LA's 'Wet Markets' Could Be On The Chopping Block - LAist

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Perspective on Pharma: Moving from academia to industry – EPM Magazine

Thursday, July 9th, 2020

In this Perspective on Pharma feature, Jung Doh, market development scientist at Beckman Coulter Life Sciences, explains how they entered the pharmaceutical industry after an unexpected opportunity arose.

As an early career scientist with a good number of years of graduate and post-doctoral training (two post-docs, actually), I made an unexpected leap: from academiawhere I thought I would spend my entire professional lifeto industry. And though it wasnt a move Id initially planned, Im the first to say that Im incredibly happy to have ended up here, since its afforded me research and personal growth opportunities I didnt even know I wanted.

After I received my doctorate in biology, I completed a post-doc in HIV research and a second, NASA-funded post-doc in the effects of microgravity on genomes. My dreamand a very concrete goal for many yearswas to become a professor at a research university, running my own lab in an area I was passionate about.

But then life intervened: my wife was offered a teaching position in Indianapolis that she couldnt pass up, so we relocated. After a few months of fruitless application to teaching and research positions at local universities, I started looking elsewhere. There are a lot of pharma and biotech companies in Indianapolis, so I started exploring some of them. In the interview process, (and much to my surprise), I discovered that they shared many of the same passions and goals I did: to benefit human health and life in fundamental and lasting ways.

The company where I ended up and still work, Beckman Coulter Life Sciences, was particularly interesting to me, since one of their key focuses was on next generation sequencing (NGS). Toward the end of my Ph.D. and in my post-doc training, NGS was becoming more routine, and I was fortunate to be able to learn and apply the techniques in my own research.

So I joined Beckman Coulter Life Sciences, which offers a range of scientific research instruments used to study complex biological problems and to advance scientific breakthroughs, first as a marketing application scientist, and then expanding into a dual role as application scientist and proof of principle scientist. In the latter, I worked with customers to develop modified protocols and tools to help research be done more efficiently. I then became product manager for our genomics product line, and as of this year, I have yet another new role, as market development scientist. In this role, I engage with the scientific community to learn from them, as well as support them to perform research better, faster, and with superior results and outcomes. I also bring the learnings and techniques gained from these collaborations to create collateral to offer other labs, or help our internal team develop product offerings for a specific need.

After making the leap into industry, I never looked back. There are, of course, benefits to both sectors. In academia, theres a certain degree of freedom and job securityonce youre tenured, that is. But it takes a lot to get tenured these daysthe funding and grants and a constant stream of publicationsparticularly in biology and related disciplines.

Though industry may seem more constrained at first glance, in many ways, theres as much or more opportunity, since there are a plethora of techniques to learn and apply in novel ways. And since technology evolves so rapidly, especially in genetic engineering and diagnostics, it seems like there are always new methods to master.

Related to this aspect, and alluded to earlier, is the strong sense that my and my colleagues work is genuinely translating into helping people across the globe. I got an inkling of that in the interview process, but its also been a palpable part of my work here. With the current pandemic, for instance, the company came together, and, within a matter of weeks, we were able to offer labs RNA extraction solutions for the virus, which are so critical right now. I felt honoured to be part of a company doing such great work, with flexibility and speed. It definitely speaks to the versatility of the industry.

Beyond the scientific, Ive learned about areas seemingly outside of science, but that are actually integral parts of the business. When I was product manager, for instance, I learned how to manage people, run meetings, build financial models, approach marketing and sales, and many other facets of the business. I had no formal business training going in, but you learn by doing, from your manager and peers. I ended up really loving all these other parts of the business of sciencetheyre challenging, but incredibly rewarding, because they push you beyond your comfort zone into uncharted areas. For that, industry has opened up areas that I didnt even know would be important, let alone fun and rewarding.

Finally, Ive been surprised and heartened by the strong sense of family that exists within a company. Part of this is felt through the opportunities for development, which is evident in all the stages I went through and all the roles Ive had. Theres a sense that staff are supported to grow as scientists and as people, which has made my accidental leap into industry all the more fulfilling.

For young scientists, theres a lot to think about when making decisions about what to study and what track to follow. I would encourage people to not get too hung up on tracks, but to stay open to the possibilitiesin other words, dont get too stuck on academia as the only option just because its where youve done your training. What really matters is having a passion for what you do, and following your interests. Genetic engineering is an area thats exploded in recent years, and will likely grow in the coming years. Ive been lucky that my own work has translated so tangibly into helping people, and at a large scalebut the same is true for many other areas in medical science. So carry onyou may end up in a totally different place from where you started, and thats not a bad thing at all.

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Perspective on Pharma: Moving from academia to industry - EPM Magazine

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COVID-19 Research: Women Are Changing the Face of the Pandemic – Genetic Engineering & Biotechnology News

Thursday, July 9th, 2020

The pristine X-ray crystallography data gathered by Rosalind Franklin played a crucial role in the discovery of DNAs structure. Yet when the discovery was recognized by the Nobel Committee in 1962, the winners of the Nobel Prize did not include Franklin, who had died in 1958. Only recently has Franklin received some of the recognition that she deserves for her essential contribution to one of the biggest discoveries of the past century.

We still have a lot of work to do, unfortunately, notes Akiko Iwasaki, PhD, an immunologist at Yale School of Medicine and a fierce advocate for women in science. Things have definitely gotten better since [Franklins] days she tells GEN. But we still have a huge disparity in women representationespecially at the senior level. Iwasaki adds that we have to address what she thinks is the root cause of the problemthe academic culture and the unconscious (or conscious) bias against women and people of color that prevents these brilliant people from moving up the academic ladder.

To mark the centenary of Franklins birth, GEN sought to highlight scientists at the forefront of COVID-19 researchsome of the most influential research currently being conductedwho are women. In this article, GEN speaks with researchers who are leading efforts to track SARS-CoV-2 genomes, to uncover host factors influencing COVID-19 progression, to develop saliva-based COVID-19 tests, and more.

Working as a pediatrician in China, Qian Zhang, MD, wanted to understand why some children are more susceptible to infections than others. Children are exposed to hundreds of pathogens every day, Zhang tells GEN, but only a very small proportion get really severe infections. Zhang has been researching differences in susceptibility for the past decade. Notably, she performed postdoctoral work at the National Institute of Allergy and Infectious Diseases (NIAID) with Helen Su, MD, PhD. Afterward, Zhang became a postdoctoral fellow at the Rockefeller University, in the laboratory of Jean-Laurent Casanova, MD, PhD.

Working with patient samples, researchers in the Casanova laboratory look for rare, deleterious mutations that might govern susceptibility to infection. In particular, they look for monogenic variants, where a single defect makes an individual far more susceptible to infection. Zhangs hypothesis for COVID-19 is that patients who are susceptible to less virulent respiratory pathogens will also be susceptible to COVID-19. By taking an unbiased approach, Zhang and colleagues may find genetic factors that have never been identified before.

Normally, Zhang analyzes children because it is in childhood that people usually experience infection for the first time. But COVID-19 is different, she notes, because this infection is the first time for everyone.

Zhang previously led the influenza team in the Casanova laboratory. So, taking on COVID-19 is a natural shift. She adds that many commonalities between the two lung infections have been established, and that many tools developed for flu research can be used in COVID-19 work. Besides, there simply arent any more flu patients coming in.

Zhang asserts that her group, like others, has adapted its work to the pandemic. Investigators normally work on well-defined infections. COVID-19, however, isnt so well defined. Too little about it is known. For example, without key pieces of data such as a fatality rate, investigators who look for genetic lesions may be unaware of the lesions prevalence. We have to change our analysis while the data are coming in, Zhang explains.

How much hesitation did Akiko Iwasaki, PhD, have in moving into COVID-19 research? None, she says. I knew the importance of speed and urgency. She notes that she had learned the value of these attributes from her experience jumping into Zika.

Iwasaki, a professor of immunobiology and molecular, cellular, and developmental biology at the Yale School of Medicine and an investigator at the Howard Hughes Medical Institute, has spent the past few months trying to understand the immune response of COVID-19 patients. Iwasakis laboratory is working to develop real-time analyses of immune markers and cytokines that could sharpen patient assessments and even inform treatmentdecisions.

The biggest surprise, so far, has been the role of interferon (IFN) in this disease, asserts Iwasaki. For other viruses, such as influenza and rhinovirus, type 1 IFN has a protective role for the host. But SARS-CoV-2 seems different. Studies in a mouse model have shown that IFN contributes to the inflammatory response without shutting down viral replication. According to Iwasaki, this is unusual. In other viral infections, IFN can shut down the virus. But Iwasaki thinks that the IFN here is being induced a little bit too late or in too small of an amount.

Iwasakis main goal is to understand what type of immune response confers protective immunity versus the types that lead to disease. Because patients have diverse responses to SARS-CoV-2, the researchers are working to build disease trajectories that reflect patient-specific aspects of the immune responsecytokine or antibody production, T-cell response, viral load, etc. By conducting longitudinal sampling and following patients trajectories, the researchers hope to predict how patients will fare when they are admitted to the hospital. Ideally, she envisions a panel that could be ordered by a physician that would allow patients to be treated with a more personalized medicine approach, based on their immune profiles.

This analysis has never been done so extensively for an infectious disease, Iwasaki asserts, because we never had the urgency to do this for other viral pathogens. In 2020, thankfully, the technology exists to do this type of analysis in real time.

Another area Iwasaki has recently explored is sex differences in SARS-CoV-2 infection. By studying male and female immune responses, her group found one clue as to why males are reportedly more susceptible to COVID-19. In a preprint posted in medRxiv, Iwasaki and colleagues described how they investigated sex differences in viral loads, antibody titers, and cytokines in COVID-19 patients, and how they found that T-cell activation was significantly more robust in women than in men. Men who dont develop a good T-cell response have worse disease outcomes.

Emma B. Hodcroft, PhD, a postdoctoral researcher at the University of Basel, recalls agreeing to keep her supervisors project going while he traveled. She was to take charge in early February. Continuity was important because they had just started uploading sequences of SARS-CoV-2 into the online genomics engine Nextstraina collaboration started in 2014 to track flu virus diversity and help predict the next flu strain.

Because Nextstrain has hubs in Europe and the United States, the absence of data uploads at the University of Basel would hamper runs during the European daytime. She has, in her own words, never looked back.

The pipeline analysis that Nextstrain runs makes phylogeny from viral genome mutations. Phylogenetics is a field full of limitations, Hodcroft notes. She adds that the field is particularly troublesome because its beautifully dangerousthe picture that is drawn is always less certain than it looks. While it is tempting to start telling stories about these sequences, she says, one must be cautious. The roughly 40,000 cases currently in the system is a drop in the bucket compared to the number of COVID-19 cases. There is much more likelihood that we havent sampled someone than we have, she admits.

As borders reopen and travel resumes, continued genomic analysis, Hodcroft tells GEN, could uncover details about virus transmission, including transmission routes. She will be keeping a close watch while cautiously communicating new findings. These data are of interest to a large and growing audience, and members of this audience may misinterpret (intentionally or not) what they hear. Deciphering the uncertainty that surrounds the field of phylogenetics requires expertisesomething not all scientists who have ventured into the world of COVID-19 phylogenetics possess.

Hodcroft gets upset when misinterpreted data spark a storyline that needs to be debunked. I dont think that telling these false stories that panic the public helps anybody, she declares. There is plenty to be worried about with this virus.

COVID-19 is the second SARS epidemic Rachel Graham, PhD, has worked on since she started her graduate work in a coronavirus lab in 2002. Currently working in a large coronavirus laboratory at University of North Carolina (UNC) led by Ralph S. Baric, PhD, she says that Barics group has scaled up from what was a busy program to an extremely busy program.

Graham uses large sequence sets to study how the virus transcriptional program contributes to replication and virulence. As the virus mutates, its subgenomic RNAs are produced in different ways, indicating that the transcription itself may be a virulence factor. She says that as the population acquires more herd immunity, researchers may see a lot of transcriptional differences in the virus, and these differences could result in changes in virulence. SARS-CoV-2 will be the first virus where this relatively new idea in virology will be examined in detail.

Lisa Gralinski, PhD, assistant professor of epidemiology at UNC, has been studying coronaviruses for 12 years. Her current work centers around virus host interactions, specifically in animal models such as the humanized ACE2 transgenic mouse. The mouse was developed at UNC in the mid-2000s after the first SARS outbreak. Researchers had even started the paperwork to cryopreserve the mouse just before COVID-19 struck. Quickly adjusting to COVID-19, they changed course and started as many breeding pairs as possible.

Graham and Gralinski may be new to the UNC faculty, but they are veterans in a rapidly growing field. Gralinski notes that six months ago, few people worked in coronavirus. Unlike SARS, SARS-CoV-2 is not currently a select agentwhich means that more people are free to work on it. Both Graham and Gralinski welcome more hands on deck, but theyve been alarmed by some of the ways that people are working with SARS-CoV-2 in their Biological Safety Level 3 (BSL3) labs. SARS-CoV-2 requires special precautions and security due to the high titers used in experiments.

In early March, Anne L. Wyllie, PhD, an associate research scientist in epidemiology at Yale, was chatting with her colleague, Nathan D. Grubaugh, PhD, an assistant professor of epidemiology. He was lamenting the level of SARS-CoV-2 RNA detection in patient samples. Wyllie drew his attention to a method she had been using to detect Streptococcus pneumoniae from saliva samples of asymptomatic carriers.

Her method, which used Thermo Fishers MagMAX Kit for Nucleic Acid Extraction, had worked so well for Wyllie that she suggested that Grubaugh use it to test for SARS-CoV-2. Wyllie recalls that when Grubaugh and colleagues compared the methods, Wyllies method blew the other one out of the water. Ultimately, the MagMAX Kit and the King Fisher platform (which happens to be named Frankie in the lab, in honor of Rosalind Franklin) became the Grubaugh laboratorys method of choice. Wyllie is now co-lead on the COVID-19 project with Grubaugh.

Wyllie was the lead author on a preprint uploaded to medRxiv showing that saliva samples offer a more sensitive and consistent alternative to nasopharyngeal swabs for COVID-19 testing. Saliva samples, the paper argued, should be considered a viable alternative to nasopharyngeal swabs to alleviate COVID-19 testing demands. This could be key to meeting public testing demands.

We knew a pandemic would come and we knew we would have to be ready, says Viviana Simon, MD, PhD, professor of microbiology at Mount Sinai School of Medicine. A decade after starting her virology laboratory in 2006, Simon and her colleagues built the Virology Initiative in 2017, which allowed real-time access to samples from patients with viral infections. The goal, she explains, was to study emerging viruses in New York Cityviruses such as Zika, chikungunya, and dengue. Having the initiative established allowed the laboratory to spring into action when the pandemic hit. Simon notes that a virology infrastructure capable of such responsiveness would not be easy to build in the middle of a pandemic.

Simon remarks that there was never any doubt that there would be a pandemic: We thought that it would be a respiratory virus and figured that it would be an avian influenza strain. Any pandemic would almost certainly come through New York City, which serves as a gateway not just for people, but for viruses from all over, she says.

Simon tells GEN that her team heard rumors about a new virus in December and began preparing. The moment the first sequences were released in mid-January, she recalls, We ordered primers. And then? Simon and colleagues waited and waited, she says, for the first case to show up. The first COVID-19 case was diagnosed at Mount Sinai on February 29. Only then could the Simon team grow the virus and sequence it.

Simons team has analyzed the genetic diversity of SARS-CoV-2 circulation in New York City and how the virus was introduced. The team is also interested in assessing the durability of antibodies and determining the degree to which antibodies are protective.

The size of Simons laboratory has doubled, primarily due to a temporary influx of postdoctoral researchers and technicians, volunteers that come from laboratories shut down by COVID-19. This COVID task force jumped in to support the COVID-19 research being done at Mount Sinai. Simon remarks that when temporary personnel start returning to their own laboratories, she will be busy hiring more people.

The dedicated researchers highlighted in this article have been working almost nonstop for months, motivated by a shared passion to beat back a virus that has taken over the world. These researchers represent different scientific backgrounds, and they are tackling different facets of the virus. But they would no doubt recognize common elements in their professional development. For example, the challenges that come with being women in male-dominated fields. Hopefully, it will not take decades to recognize and celebrate the contributions of some of these outstanding scientists.

Original post:
COVID-19 Research: Women Are Changing the Face of the Pandemic - Genetic Engineering & Biotechnology News

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