‘Anatomy of Black Love’ creators want to change the narrative on relationships – Rolling Out

Sol Aponte and Jennia Fredrique-Aponte (Photo credit: Richard-Luc Elie)

We know what the statistics say. Marriage rates are low while the divorce rate is high. Even if you ignore the statistics, you wouldnt have to look very far on any social media platform before youll see explanations behind this discrepancy in the Black community. Because, although we smile fondly at images of Barack and Michelle Obama and aspire to have the business relationship of Beyonc and Jay-Z, many of us cant seem to create that type of synergy in our own relationships.

Black men and Black women are often on polarizing sides of the relationship conversation, with both sides crying victim on social media. Sol Aponte and Jennia Fredrique-Aponte, creators of Revolts popular documentary series, Anatomy of Black Love, want to change the narrative in the Black community when it comes to the importance of a happy and healthy relationship. Rolling out asked the fashion-forward married couple for their take on how couples can help change the negative narrative on relationships in our community.

How can the Black couples change the narrative on Black love so that more singles will let their guard down and embrace the idea of a healthy relationship?

Fredrique-Aponte: I think it is in our nature to love and want to be loved. Our work is to discern and educate ourselves on what works best for each of us. The term equally yoked should not be taken lightly.

Aponte: Changing the narrative takes action: action on the part of anyone wanting to see that change. In order to attract a healthy relationship, a person has to first begin with loving themselvesperiod. Next, a person has to be honest with themselves, about themselves. Oftentimes we think we show up in ways that we dont. Be honest about the feedback youve received from prior relationships and own your own -ish. When you are honest about who youve been, you can work on being the person youd want to attract.

For more information on Anatomy of Black Love visit http://www.revolt.com.

The principal behind Enchanted Branding & PR, a premier entertainment agency based in Atlanta. She also is a media trainer/ consultant and pop culture analyst. Self-proclaimed feminist and equestrian-in-training. You can see more of Christal on her website http:musiclivelifeshow.com

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'Anatomy of Black Love' creators want to change the narrative on relationships - Rolling Out

Before ‘Council of Dads,’ Michael O’Neill was the shooter on ‘Grey’s Anatomy’ – EW.com

Council of Dads' Michael O'Neill was the shooter on Grey's Anatomy | EW.com Top Navigation Close View image

Before Council of Dads, Michael O'Neill was the shooter on Grey's Anatomy

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How Did FBI And FBI: Most Wanted’s Crossover Compare To One Chicago And Grey’s Anatomy? – CinemaBlend

Oddly enough, I have mixed feelings. I'm left with the sense that FBI and FBI: Most Wanted are currently more similar to Grey's Anatomy and Station 19, and not just because the shows don't have a name for the shared universe, a la One Chicago or the Arrow-verse over on The CW. (For simplicity's sake, I'm going to just refer to the two CBS series as the FBI-verse.) Despite the parallels between the FBI-verse and Grey's/Station 19, however, I see the potential for the FBI-verse to become more like One Chicago down the line.

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How Did FBI And FBI: Most Wanted's Crossover Compare To One Chicago And Grey's Anatomy? - CinemaBlend

‘Grey’s Anatomy’ and other TV shows donate medical supplies to real doctors fighting coronavirus – Yahoo Lifestyle

As the coronavirus pandemic continues to grow worldwide, it looks like television's most popular medical shows are doing their part to help fight the spread of the virus specifically by lending a hand to health care workers who are increasingly facing a shortage of medical supplies amid the crisis.

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'Grey's Anatomy' and other TV shows donate medical supplies to real doctors fighting coronavirus - Yahoo Lifestyle

‘Grey’s Anatomy’ And Other Medical TV Shows Are Donating Their Masks And Gloves To Real Doctors Fighting Coronavirus – Simplemost

Medical supplies are high in demand and short in supply amid the global coronavirus crisis, and now, help is coming from an unexpected source: television shows.

Medical dramas including Greys Anatomy, Station 19 and The Resident are all donating surgical gloves and masks that are used as props on the shows to aid real-life doctors in the fight against the virus.

At Station 19, we were lucky enough to have about 300 of the coveted N95 masks which we donated to our local fire station, Krista Vernoff, executive producer of ABCs Greys Anatomy and Station 19 told Good Morning America in a statement. They were tremendously grateful. At Greys Anatomy, we have a back-stock of gowns and gloves which we are donating as well. We are all overwhelmed with gratitude for our healthcare workers during this incredibly difficult time, and in addition to those donations, we are doing our part to help them by staying home.

Amazon

While the United States has a stockpile of 13 million N95 respirator masks, the government predicts that as many as 1 billion masks might be needed in the next six months.

Other television shows that will be making similar donations include The Good Doctor and Filthy Rich, which will donate cleaning supplies and food pallets.

This kind of community support means so much to our #frontlineproviders who are making many sacrifices to staff our hospitals and care for our community, Dr. Karen L. Law, program director of Internal Medicine Residency Program at Emory University, told CNN of the donations her team received from The Resident.

She took to Instagram to express her gratitude:

View this post on Instagram

"Look for the helpers. You will always find people who are helping." . To the entire team @theresidentonfox, thank you for this incredibly generous donation of #PPE from your set, including gowns, masks, gloves, and all the things our healthcare workers need to provide safe care for our community during #COVID19. . Yesterday, I had a serious discussion with the residents about how, though supplies are low, a magical shipment of masks is unlikely to arrive. And yet, a magical shipment of masks DID arrive, in the form of this very generous gesture. This kind of community support means so much to our #frontlineproviders who are making many sacrifices to staff our hospitals and care for our community. . Thank you, @theresidentonfox and @foxtv for being helpers. We needed this kind of good news today. . PS: Sorry it's not a great pic, but the focus was not on the photo at the time. Similarly, the team @theresidentonfox are good citizens doing good deeds and not looking for a shout out. Though I encourage all to support The Resident and the great team behind the show and to pay their good deed forward any way you can. . #Hurstlife #residentlife #emoryIMresidents #lookforthehelpers #gratitude

A post shared by klaw (@karen.ll.law) on Mar 18, 2020 at 12:27pm PDT

Yesterday, I had a serious discussion with the residents about how, though supplies are low, a magical shipment of masks is unlikely to arrive, she wrote. And yet, a magical shipment of masks DID arrive, in the form of this very generous gesture.

This personal protective equipment is much needed right now to keep our health-care workers and first-responders safe! Kudos to these shows for pitching in however they can.

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'Grey's Anatomy' And Other Medical TV Shows Are Donating Their Masks And Gloves To Real Doctors Fighting Coronavirus - Simplemost

‘Grey’s Anatomy’ Star Caterina Scorsone Shares The Sweetest Video With Daughter Paloma on Instagram – Showbiz Cheat Sheet

Caterina Scorsone ofABCsGreys Anatomyrecently welcomed third daughter Arwen with husband Rob Giles on December 31. The newborn joins sisters Eliza, 7, and Paloma (whom they call Pippa), 3, keeping the star of themedical dramabusy with a full family life.

The Greys Anatomy actress has previously spoken on Pippas diagnosis of Down syndrome and how it changed her view of parenting. In celebration of World Down Syndrome Day, Scorsone and her 3-year-old recently took to social media to showcase the little girls alphabet skills.

Scorsone often does her part to shine a light on Down syndrome in the hopes of dispelling the misconceptions about the genetic disorder. In October, the actress posted an adorable pic of Pippa to spotlight Down Syndrome Awareness month and present a few facts on the condition and emphasize the importance of verbiage.

Heres a little info. 1 in 700 babies is born with Down syndrome, Scorsone captioned the close-up of Pippa on Instagram. Language is important. Parents dont have a 1 in 700 RISK of having a baby with Down syndrome. Parents have a 1 in 700 CHANCE of having a baby with Down syndrome, just like they have a 50 percent CHANCE of having a girl and a 50 percent CHANCE of having a boy. (With some beautiful variations in there as well).

The Greys Anatomy star went on to encourage people to choose their words carefully when talking about Down syndrome, sharing that children with the disorder are a blessing. Differences are beautiful. Language changes how people think, Scorsone wrote. Words are important. #hitthejackpot#theluckyfew#nothingdownaboutit#love

With Saturday being World Down Syndrome Day, Scorsone and Pippa decided to show off their alphabet skills in an Instagram video. With the actress leading the duo by signing each letter with her hands while Pippa announced them as they went along, the two celebrated when they got to Z.

Yay! Pippa is smart! Scorsone cheered her daughter while signing smart in sign language, inspiring Pippa to copy the gesture.

Happy World Down syndrome awareness day, everybody!! Scorsone captioned the heartwarming video, according to People. Sending love and alphabets from our family to yours!! .

The mom of three has previously shared how she felt unsure of the best way to parent Pippa when she was first diagnosed.

I dont know what Im supposed to do, I dont know what I am as a mother, how do I mother this child? Scorsone recalled on a Motherly podcast, according to Today.com. If my job isnt to equip her to compete or dominate socially, educationally or physically or economically if Im not just supposed to be helping her do that, what is a mother, what is my job?

Scorsone eventually had an epiphany on what her true role as a mother entailed, as well as what it meant to genuinely love others.

I had to confront that thought experiment of I dont know if [Pippa is] going to be clever, I dont know if shes going to be funny which, of course, she is, and nowthat I know more about Down syndrome, Im like, Oh, what a stupid thought I had, she said, according to People. But I didnt know, and it forced me to realize that I was loving my other daughter and everyone, including myself, for absolutely the wrong reason. I was loving people for their external qualities and not for their essence.

Scorsone shared that she feels extreme gratitude at being given the gift of parenting someone as special as Pippa. It shows you that, Okay, this is a totally different journey, but theres something mystically special about this journey, Scorsone said. You can embrace it in a way that is like, Wow, one in 700 people get to experience this and Im one of them.

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Bruker Announces Launch of CE-IVD Marked genesig Assay Kit for the Detection of the SARS-CoV-2 Virus – Yahoo Finance

Bruker Corporation (Nasdaq: BRKR) today announced a distribution agreement with Primer Design Ltd (UK), a subsidiary of Novacyt SA, for Bruker-Hain Diagnostics to distribute the CE-IVD-labeled genesig real-time PCR coronavirus (COVID-2019) assay, effective immediately. Bruker-Hain Diagnostics has a portfolio of DNA/RNA extraction and preparation systems and kits.

The genesig real-time PCR Coronavirus (COVID-2019) CE-IVD assay is validated for use on Bruker-Hain Diagnostics GenoXtract (GXT) automated nucleic acid extraction devices with associated extraction kits. Shipments to Spain, France, Germany and the UK have already started.

The genesig assay has been validated for respiratory samples (nasopharyngeal swabs, oropharyngeal swabs, sputum) on commonly available laboratory thermocyclers. The kit includes all necessary reagents to produce up to 96 results in under two hours. The genesig assay is designed for very high specificity for the 2019-nCoV virus strain that is implicated in COVID-19. The genesig test is CE-IVD marked and intended for in vitro diagnostic use in Europe.

Graham Mullis, CEO of Novacyt SA, stated: "With Bruker we have found a strong distribution partner with a Microbiology & Diagnostics business that has significant reach into a large number of European infectious disease laboratories. This will help to bring our genesig test into laboratories quickly, where its diagnostic results can help to prevent the further spreading of COVID-19."

Dr. Wolfgang Pusch, Executive Vice President Microbiology & Diagnostics at Bruker Daltonics, commented: "Bruker is joining the fight against COVID-19. In combination with our validated GenoXtract (GXT) products for nucleic acid extraction, we now offer a solution for preparation and detection of the SARS-CoV-2 virus. We have also seen accelerated orders of our MALDI Biotyper systems from Chinese CDC laboratories, e.g. to rule in or out bacterial infections in severe respiratory disease."

About Bruker-Hain Diagnostics

Bruker-Hain Diagnostics is focused on Molecular Diagnostics (MDx) products within Brukers Microbiology & Diagnostics business. Hain Lifescience GmbH is the legal manufacturer of the Fluorocycler XT, MTBDR 2.0 assay and of GXT nucleic acid preparation kits. For more information, please visit, http://www.hain-lifescience.de.

About Bruker Corporation (Nasdaq: BRKR)

Bruker is enabling scientists to make breakthrough discoveries and develop new applications that improve the quality of human life. Brukers high-performance scientific instruments and high-value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity and customer success in life science molecular research, in applied and pharma applications, in microscopy and nanoanalysis, and in industrial applications, as well as in cell biology, preclinical imaging, clinical phenomics and proteomics research and clinical microbiology. For more information, please visit: http://www.bruker.com.

View source version on businesswire.com: https://www.businesswire.com/news/home/20200324005721/en/

Contacts

Investor Contact: Miroslava MinkovaDirector of Investor Relations and Corporate DevelopmentT: +1 (978) 6633660, ext. 1479E: miroslava.minkova@bruker.com

Contact for Media and Customers: Philip PerryBruker DaltonicsT: +49-172-313-7216E: Philip.Perry@bruker.com

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A new AI system has enabled the discovery of a novel role for ‘smell-sensing’ genes in colon cancer – Healthcare IT News

Humans havearound400olfactorysmell-sensing genes the largest gene familyin humansthat are turnedon in the noseand other parts of the body, allowing us to smell at least one trillion different odours.Up until now, the role of theseolfactorygenes outside the nose has been largely unknown.

A recent study, published in Molecular Systems Biology, usedmultiple layers of artificial intelligence (AI) toidentifythesegenes involved inthe organisation ofcolon cancer cells. Thisrevealed thatsmell-sensinggenescancontribute to this cancer-associated processalong with keycoloncancer genesandhighlighted their potential role indisease spread andprognosis.

The discoverywas enabled by thedevelopmentof an innovativeAI system, calledKnowledge-and Context-driven Machine Learning (KCML)that enables researchers to studymicroscopy imagesin greater detail to understand more about the function of genes in specific context. KCML has first been applied to colon cancerbut is widely applicable in other diseases too.

The researchers usedcomputer vision algorithm to detect changes in cell appearance and organisation. The algorithm was fed information from robotic microscopy, in collaboration with researchers from the University of Zurich, to image millions of colon cancer cells.By reducing the expression of the smelling genes within these cells, they were able to understand more about the role they play in carcinogenesis.

Expression is whengenes are activated to produce certain proteinsand molecules. Researchers in this study found that reducing the expression of smell-sensing genes in colon cancer cells, a process known as perturbation,can inhibit cells from spreading, potentially by restraining the ability of cells to move. The same behaviour is also observed in the perturbation of key cancer genes.

Dr Heba Sailem,Sir Henry Wellcome Research Fellow at theInstitute of Biomedical Engineering in the UK, alead author on the study,explained: With all this big imaging data, we have a powerfulmeans tobetter understand how every single gene contributes to cancer cell behaviour. I have developed an AI system that is guided by prior knowledge of gene function that allows us to learn much more from this data than would be possible using existing methods.

When humans look atcomplex scenes, theyinterpret the images in light of their previous experience and visual memories (prior knowledge). However, computersjust seeimages asalargematrix of numbers, they will not see shapes and structures.Computer vision is about training the computer to see whatthe human can see. Through AI, we are able to identifyhow turning genes off affectsthe characteristics, shape and structureof cells and tissue. Usually, it is a very lengthy process for humans to interpret numbers from thousands of images, each with thousands of cells.Computer vision can achieve that in a few days,she added.

Dr Sailemswork has focussed on studying cells in culture, and the next step will beto link these findingsthroughto real patient data. She is also keen to apply her AI modelto study the behaviour of genes indifferent cancers, including prostrate, breast and lung.

WHY IT MATTERS

Colorectal cancer is the third most common cancer in the UK and the second most common cause of cancer deaths.

Professor Mark Lawler, chair in translational cancer genomics, Centre for Cancer Research and Cell Biology, Queens University Belfast and Bowel Cancer UK medical advisor,welcomed the application of the new AI model in colorectal cancer, commenting the study showed the power of data in revealing new mechanisms.

One of the biggest challenges in colorectal cancer is metastasis. This is the point at which most patients die. Something that tells us more about that and maybe indicates how this could be controlled is verypromising, he added.

Dr Sailem explained:Cancer is not one disease - itcan be classified intomany diseases depending ontissue type and origin. Wecan takecellsfrom diseased tissueand look at what the genes in theseparticular cellsare doing. We can then identify genes to target for therapy or genesfor which targeted therapies already exist.

THE LARGER TREND

AIand machine learningis increasingly being used to acceleratethe development oftargeted therapies in cancer and other diseases, with leading technology and pharmaceuticalcompanies forming high profile partnerships in recent months.

One such collaboration between Novartis and Microsoft was announced in October to transform medicine with AI. Vas Narasimhan, CEO of Novartis, said, As Novartis continues evolving into a focused medicines company powered by advanced therapy platforms and data science, alliances like this will help us deliver on our purpose to reimagine medicine to improve and extend lives. Pairing our deep knowledge of human biology and medicine with Microsofts leading expertise in AI could transform the way we discover and develop medicines for the world.

ON THE RECORD

Professor Tim Maughan,professor of clinical oncology at the University of Oxford and advisor to Bowel Cancer UK,saidDr Sailemsstudy linked to his own research into howcellswithin tumourstalkto each other.

He said: What they say to each other is determined by molecular make up but also by the conversation going on between the cells. The shape that the cellshave, theway that theyareorganised, the distance they are apart, how close the immune cells get into the cancer,is all a result of the conversation going on between the different cell types within a cancer

DrSailemin this study has found that inadditiontoidentifyingwhole new genes which are important in bowel cancer, she has also picked up that genes that are part of thatolfactorysmell system play a part of this conversation.

Commentingon the research, Professor Lawler said:It is saying something about why there areolfactorygenes in other parts of the body and how they might be responding to the microbiome in the gut. It will be interesting to see what stimulates these genes to upregulate or down regulate in their environment. From there we may be able to identify important biomarkers.

He added: Big data for better health makes sense. You can use that data to change lives, diagnose patients earlier, develop better treatment and improve their quality of life and above all, data can really save lives.

For more information on bowel cancer go to http://www.bowelcanceruk.org.uk.

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Meet a superhero that fights breast cancer, neurofibromin – Baylor College of Medicine News

It is well known that neurofibromin (NF1), a tumor suppressor produced by the NF1 gene, keeps cancer growth in check by repressing the activity of a cancer driver gene called Ras. It then follows that when NF1 is lost, Ras can drive cancer growth by promoting treatment resistance and metastasis. NF1, however, can do more than regulate Ras.

Drs. Eric C. Chang, Matthew Ellis and Zeyi Zheng at Baylor College of Medicine and their colleagues have discovered new insights into the function of neurofibromin that improve our understanding of breast cancer resistance and suggest novel therapeutic approaches to overcome it.

The team first studied the importance of neurofibromin loss in a study they published in 2018. In this study, they sequenced tumor DNA seeking for mutations that can promote resistance to tamoxifen, a drug commonly used to prevent relapses from estrogen receptor positive (ER+) breast cancer.

When we examined the mutational patterns in NF1, we observed that poor patient outcome only occurred when neurofibromin was lost, not through mutations that selectively affect Ras regulation. This suggested that neurofibromin may have more than one function, said Chang, co-corresponding author of this work and associate professor in the Department of Molecular and Cellular Biology and a member in the Dan L Duncan Comprehensive Cancer Centers Lester and Sue Smith Breast Center.

This thought triggered studies, spearheaded by Zheng in Changs lab, into the function of neurofibromin in ER+ breast cancer cells. One of his early experiments showed that when expression of NF1 is inhibited (to mimic neurofibromin loss in tumors), the resulting ER+ breast cancer cells were stimulated by tamoxifen instead of inhibited, as it usually happens. Furthermore, these neurofibromin-depleted cells became sensitive to a very low concentration of estradiol, a form of estrogen.

The clinical relevance of these findings was immediately apparent because it suggested that tamoxifen or aromatase inhibitors, which lower estrogen levels available to the cancer cells, would be the wrong choice for treatment when neurofibromin is lost by the tumor, said Ellis, co-corresponding author and professor and director of the Lester and Sue Smith Breast Center. Dr. Ellis also is a McNair Scholar at Baylor.

Follow-up gene expression studies all strongly suggested that neurofibromin behaves like a classic ER co-repressor.

A co-repressor must bind ER directly, but the group hesitated to conduct such an experiment without more evidence because it is not trivial to do so, Chang said.

A breakthrough came when Dr. Charles Foulds, a co-author on the paper and assistant professor at the Center for Precision Environmental Health at Baylor, searched the Epicome, a massive proteomic database created by Dr. Anna Malovannaya and Dr. Jun Qin, also at Baylor. This is a part of an effort by Dr. Bert OMalley, chancellor and professor of Baylors Department of Molecular and Cellular Biology to comprehensively document all the proteins associated with ER.

Foulds found neurofibromin in the database, which encouraged the team to ultimately investigate whether estrogen receptor and neurofibromin interacted directly. However, to seriously consider NF1 as an ER co-repressor, there was still another missing piece of the puzzle.

One day Charles casually asked me whether neurofibromin had a region rich in the amino acids leucine and isoleucine, because co-repressors use these regions or motifs to bind ER, and it dawned on me that neurofibromin indeed does, Chang said. In fact, neurofibromin has two such motifs that mediate ER binding in a cooperative manner. These motifs are frequently mutated in cancer, but are not required for Ras regulation.

Since tamoxifen or aromatase inhibitors were found to be ineffective for neurofibromin-deficient ER+ breast cancer tumors, the researchers worked with animal models to determine whether the ER-degrading drug fulvestrant was still effective. However, fulvestrant only temporarily inhibited tumor growth because secondary Ras-dependent fulvestrant resistance was induced by neurofibromin loss. This Ras-dependent growth phase could be inhibited with the addition of a MEK inhibitor, which shuts off a key signaling pathway downstream of Ras.

The team validated this combination treatment strategy using a patient-derived xenograft (PDX) mouse model. In this model, a section of a human tumor taken from a patient is directly transplanted into a mouse under conditions that maintain the genomics and drug response of the original human tumor from which it was derived (Cell Reports, 2013). In this case, this PDX was derived from a patient who failed several lines of endocrine therapy and had already developed fulvestrant resistance.

The results of the combination of fulvestrant to degrade ER and a MEK inhibitor (e.g., selumetinib or binimetinib) to inhibit Ras downstream signaling, were encouraging the tumor shrunk to almost undetectable levels, Chang said.

Our next goal is to test this combination therapy in clinical trials in order to determine its therapeutic potential in the clinic.

Neurofibromin is lost in at least 10 percent of metastatic ER+ tumors. As a result of these new data, we are now working on a clinical trial that combines a MEK inhibitor with fulvestrant, said Ellis, Susan G. Komen scholar and associate director of Precision Medicine at the Dan L Duncan Comprehensive Cancer Center at Baylor. Interestingly, MEK inhibitors are also being used to control peripheral nerve tumors in patients with neurofibromatosis, where a damaged NF1 gene is inherited. Our findings contribute to an understanding of why female neurofibromatosis patients also have a much higher incidence of breast cancer.

Other contributors to this work include Meenakshi Anurag, Jonathan T. Lei, Jin Cao, Purba Singh, Jianheng Peng, Hilda Kennedy, Nhu-Chau Nguyen, Yue Chen, Philip Lavere, Jing Li, Xin-Hui Du, Burcu Cakar, Wei Song, Beom-Jun Kim, Jiejun Shi, Sinem Seker, Doug W. Chan, Guo-Qiang Zhao, Xi Chen, Kimberly C. Banks, Richard B. Lanman, Maryam Nemati Shafaee, Xiang H.-F. Zhang, Suhas Vasaikar, Bing Zhang, Susan G. Hilsenbeck, Wei Li and Charles E. Foulds. The authors are affiliated with one or more of the following institutions: Baylor College of Medicine, Chongqing Medical University, Adrienne Helis Malvin Medical Research Foundation, Zhengzhou University and Guardant Health.

This work appears in Cancer Cell,

See the publication for a complete list of the sources of support for this work.

By Ana Mara Rodrguez, Ph.D.

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What India must do to break the Covid-19 chain – Economic Times

Early in March, India became the fifth country in the world to sequence the genome of the novel Coronavirus, or Covid-19, and share its data with the international community.

Pune-based National Institute of Virology, an institution under the Indian Council of Medical Research, the countrys nodal health research body, sent the first two data sets to an open database shared by researchers globally.

Labs, largely from China, the United States and the Netherlands, have so far contributed just over 1,100 samples to the database, which researchers across the world can use to analyse and work on tests, vaccines and drugs to combat the pandemic.

In India, the first set of genome data -- detailing the complete DNA of the virus came from individuals in Kerala who had contracted the virus.

The volume of the sample and the concentration of the virus play a crucial role during the sequencing of the virus genome. In some samples that we received, there was less virus concentration and in case of clinical samples, sometimes the volume was less. These were some of the challenges, says Professor Priya Abraham, Director of the National Institute of Virology.

The SARS-CoV2 genome, as it is formally known, has about 30,000 base pairs, somewhat like a long string with 30,000 places where each one of these occupy one of four chemicals called nucleotides. This long string, with its unique combination of nucleotides, is what uniquely identifies the virus and is called its genomic sequence. To put that in context, a human genome, which is more complex, has 3 billion base pairs.

Genome data is essential to build tests, find drugs and vaccines. It is also needed to figure out if there has been a mutation of the virus and how that will affect different populations. It is also key to finding measures to deal with its spread.

We need to know how the virus mutates, correlate sequence variation and its severity on patients, says Professor S Vijaya of the Department of Microbiology and Cell Biology at the Indian Institute of Science who has done extensive research on tuberculosis and the Japanese Encephalitis virus.

Scientists are of the view that India needs to sequence more strains as the virus mutates.

It is important to understand whether there are new variants, why is a cluster seeing more serious patients and some milder? Vijaya says. In Italy, the fatality rate is in 10% of the infected patients, in China it was 2%. We need to isolate strains that have a sequence variation that are more pathogenic, she adds.

The novel Coronavirus, whose initial host is suspected to be a bat, originated in Hubei province of China last December.

China was initially slow to realise the magnitude of the virus, which affects the respiratory organs. Since then, the contagious disease that spreads through droplets, either through saliva or when a person coughs or sneezes, has turned into a global pandemic.

There is no vaccine or drug yet for the outbreak that has killed thousands, largely people with underlying medical conditions such as cardiac, diabetes and respiratory problems.

So far, the most effective measure has been to isolate people who have tested positive, quarantine them and increase social distancing to contain its spread.

India has seen the disease enter the third phase of community spread -- people who have not had any contact with those infected, testing positive for the virus.

On Monday, the World Health Organisation warned that the pandemic was accelerating.

It took 67 days for cases to reach the 100,000 mark globally, 11 days to hit 200,000 and just four days to touch 300,000 cases.

So far, more than 6,000 people in Italy have died from the virus, surpassing even that of China. More than 16,500 people have died across the world.

Given the severity of the problem and the global lockdowns in place, India needs to do more sequencing of the virus before it spreads, researchers say.

Since reporting its first positive case on January 30, the country has seen that number swell to more than 500, and nine people dead so far.

If we do more sequencing, we can identify what is the rate of change in the virus, how it is spreading and the how much of the virus (based on its variations) is there in the population, says Chitra Pattabiraman, India Alliance Early Career Fellow at the Department of Neurovirology of the Bengaluru-based National Institute of Mental Health and Neurosciences (Nimhans).

Pattabiraman, a virologist who has done genome sequencing to identify pathogens in brain infections, says sequencing in the earliest phases of an outbreak is valuable because it helps in faster decision making on how to tackle its spread.

India should sequence more strains so that it can contribute to research globally, she says.

We need to develop more capacity and share more strains with the global network. We have forever used other peoples databases for our research, this provides us the opportunity to contribute to the world community, she says.

The country has around 40 labs, including at the Indian Institute of Science and Manipal University, that have the required bio-safety limits (BSL-3) for sequencing the virus, yet it has not opened up the samples to labs outside of the ICMR network.

If more labs are allowed to get into studying the strains, I think we can get more understanding of the virus, says Professor Vijay Chandru, cofounder of Strand Genomics, which was among the first private labs to receive permission to test samples of Covid-19 infections.

ICMR is cautious about opening up more labs for genome sequencing because of the stringent standards required to extract the strains, Chandru says.

Lots of people have capabilities, doing this right is important.

Availability of the Indian sequences will help in understanding the diversity of the viral sequences circulating in the country and its similarities with global strains, Abraham of NIV says.

This would further help in designing specific primers, develop vaccines and drugs that would work better, and local companies would benefit, she says.

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What India must do to break the Covid-19 chain - Economic Times