Home Featured DNA may hold the key to protecting populations from COVID-19FeaturedGeneticsNeuroscience·April 30, 2020The test is based on technology developed through the DNA Zoo project, a global initiative that analyses DNA from different species to help researchers, leaders and policy-makers better understand species through their DNA as well as threats to their survival. Image is in the public domain. Summary: A new genetics test for COVID-19 has been developed by an international team of researchers. The full genome sequencing test can not only provide accurate results in less than two minutes, but it can also extract intricate and highly complex genetic data about the strain of the coronavirus infection. Source: University of Western Australia Scientists from The University of Western Australia’s Faculty of Science are part of a global team that is developing a new DNA test for COVID-19, which can provide faster and more detailed results than other tests. This test can be used to understand how COVID-19 is mutating, aid vaccine development and understand its journey across populations globally—for instance, how it adapts to a new host. It is currently being used for COVID-19 research, but once approved by the US Food and Drug administration it can be used for both the diagnostic testing of patients and to enable a better understanding of the virus. The test is based on technology developed through the DNA Zoo project, a global initiative that analyses DNA from different species to help researchers, leaders and policy-makers better understand species through their DNA as well as threats to their survival. Dr. Parwinder Kaur, from UWA’s School of Agriculture and Environment, who is the Australian project lead, said the new test would enable one person to process hundreds of samples a day, at a cost comparable to current tests. “Following full genome sequencing, the results can be processed rapidly in less than two minutes using local high-performance computing software through WA’s Pawsey Supercomputing Centre, Microsoft and the technology company DUG.” First author of the study, Brian St Hilaire, graduate student from The Aiden Lab—Baylor College of Medicine, said that the preliminary testing approach published on bioRxiv, provided more than just a positive or negative result for the virus. “Instead, this test extracts intricate and highly complex genetic data surrounding the strain of the virus and its behaviour,” he said. Project lead Dr. Aviva Presser Aiden, from the Baylor College of Medicine, said as COVID-19 continued to spread across the world, global healthcare systems faced significant challenges. “Extensive diagnostic testing is integral to disease control,” Dr. Aiden said. “This test will help us understand a number of unknowns about the disease and its transmission.” Dr. Kaur said because the test was able to detect low viral concentrations compared to other diagnostic tests, it could also be used to monitor COVID-19 through wastewater treatment plants to track its spread through communities. “We hope the test will provide important new insights into the infection by analysing the genetic makeup of the virus which will assist with disease control into the future,” she said. “For years to come, humans will be co-existing with animals that can transmit diseases like COVID-19, so understanding the genetic makeup and behaviour of these diseases is going to be vital in preparing us for pandemics in the future.”.See alsoauditory neuroscienceFeaturedNeuroscienceOpen Neuroscience Articles·May 12, 2020How the brain responds to the sudden sound of silent danger About this COVID-19 research article Source: University of Western Australia Media Contacts: Press Office – University of Western Australia Image Source: The image is in the public domain. Original Research: Closed access A rapid, low cost, and highly sensitive SARS-CoV-2 diagnostic based on whole genome sequencing”. by Brian Glenn St Hilaire et al. bioRxiv doi:10.1101/2020.04.25.061499 Abstract A rapid, low cost, and highly sensitive SARS-CoV-2 diagnostic based on whole genome sequencing Early detection of infection with SARS-CoV-2 is key to managing the current global pandemic, as evidence shows the virus is most contagious on or before symptom onset1,2. Here, we introduce a low-cost, high-throughput method for diagnosis of SARS-CoV-2 infection, dubbed Pathogen-Oriented Low-Cost Assembly & Re-Sequencing (POLAR), that enhances sensitivity by aiming to amplify the entire SARS-CoV-2 genome rather than targeting particular viral loci, as in typical RT-PCR assays. To achieve this goal, we combine a SARS-CoV-2 enrichment method developed by the ARTIC Network (https://artic.network/) with short-read DNA sequencing and de novo genome assembly. We are able to reliably (>95% accuracy) detect SARS-CoV-2 at concentrations of 84 genome equivalents per milliliter, better than the reported limits of detection of almost all diagnostic methods currently approved by the US Food and Drug Administration. At higher concentrations, we are able to reliably assemble the SARS-CoV-2 genome in the sample, often with no gaps and perfect accuracy. Such genome assemblies enable the spread of the disease to be analyzed much more effectively than would be possible with an ordinary yes/no diagnostic, and can help identify vaccine and drug targets. Using POLAR, a single person can process 192 samples over the course of an 8-hour experiment, at a cost of ~$30/patient, enabling a 24-hour turnaround with sequencing and data analysis time included. Further testing and refinement will likely enable greater enhancements in the sensitivity of the above approach. Feel Free To Share This Genetics News. 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