A University of York virologist is helping to analyze the genetic codes – or the blueprint – of the SARS-CoV-2 virus that causes COVID-19.
The findings will help researchers better understand how strains of the virus evolve and help identify new clusters of the virus.
Analyzing global data on the published genome sequences of this novel coronavirus will help fast track our understanding of this complex disease.
The researchers, from The Commonwealth Scientific and Industrial Research Organisation (CSIRO) in Australia, developed a novel visualization platform, underpinned by bioinformatics algorithms originally used to analyze the human genome, to pinpoint differences among the thousands of genetic sequences of the SARS-CoV-2 virus.
CSIRO Chief Executive Dr Larry Marshall said knowing the genetic code was vital.
Dr Marshall said: “The more we know about this virus, the better armed we’ll be to fight it. This highly complex analysis of the genome sequence of the SARS-CoV-2 virus has already helped to determine which strains of the virus are suitable for testing vaccines underway at the Australian Centre for Disease Preparedness in Geelong – the only high biocontainment facility of its kind in the Southern Hemisphere.”
Professor Seshadri Vasan – who holds an honorary chair at the University of York and is CSIRO’s Dangerous Pathogens Team Leader – is leading the SARS-CoV-2 virus work and vaccine evaluation studies and is the corresponding author of the study.
He said the first 181 published genome sequences from the current COVID-19 outbreak were analyzed to understand how changes in the virus could affect its behavior and impact.
Dr Vasan added: “This RNA virus is expected to evolve into a number of distinct clusters that share mutations, which is what we have confirmed and visualized. At this time, we do not expect it will affect the development and evaluation of COVID-19 vaccines, therapies and diagnostics, but it is important information to monitor as preclinical and clinical studies progress.
“To enable this, we are calling on the international research community to share de-identified details of case severity and outcome, and other relevant meta-data such as co-morbidities and smoking status, alongside the genomic sequences of the virus.”
CSIRO’s Bioinformatics Team Leader Dr Denis Bauer said as the virus evolves, this blueprint becomes increasingly important, effectively because it holds instructions about the behavior of the virus and what kind of disease it can cause.
First author, Dr Bauer said: “Globally there is now a huge amount of individual virus sequences. Assessing the evolutionary distance between these data points and visualizing it helps researchers find out about the different strains of the virus – including where they came from and how they continue to evolve.
“The advantage of the data visualization platform is that it highlights evolving genetic mutations of the virus as it continues to change and adapt to new environments.
“The more informed we are about the genetic differences and their likely consequences on the progression of the disease, the better we can tackle the disease with diagnostics and treatments.”
CSIRO’s Australian e-Health Research Centre CEO David Hansen said the work shows the importance of cross-collaboration between the established and emerging disciplines of bioinformatics, genomics, vaccinology and virology.
“Following the scientific process of peer-reviewed open publication such as this one is a vitally critical component of the CSIRO’s response.”
Bauer et al. (2020) Supporting pandemic response using genomics and bioinformatics: a case study on the emergent SARS‐CoV‐2 outbreak. Transboundary and Emerging Diseases. DOI: https://doi.org/10.1111/tbed.13588
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