SARS-CoV-2 genetic diversity and stability in the presence of neutralising antibodies and antivirals

  • Funded by UK Research and Innovation (UKRI)
  • Total publications:3 publications

Grant number: BB/V013874/1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $154,513.57
  • Funder

    UK Research and Innovation (UKRI)
  • Principal Investigator

    DA Matthews
  • Research Location

    United Kingdom
  • Lead Research Institution

    University of Bristol
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Pathogen genomics, mutations and adaptations

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

We want to understand how the SARS-CoV-2 virus (which causes COVID-19) might mutate when it is placed under what is known as selective pressure. At the moment the virus is spreading around the globe and it is mutating relatively slowly. That is likely to be because nobody has any pre-existing immunity top the virus and we have limited effective drugs that target the virus and even the one drug we do have that targets the virus (Remdesivir) has not been widely used. Over time we anticipate that more and more people will become immune because they have had the virus or because they have had a vaccine. At the same time, we believe that drugs that directly target the virus will become available and more widely used. Once this happens the virus will find it harder to spread and cause serious disease and when that happens it is possible that the virus will begin to accumulate mutations that will help it to evade the drugs we have developed and the vaccines we have deployed. This project will recreate that kind of evolutionary pressure in the laboratory so we can understand what kinds of mutations might emerge or even if the virus is actually unable to mutate and that the vaccines being planned and the antiviral drugs being evaluated will be effective over many years.

Publicationslinked via Europe PMC

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Nanopore ReCappable sequencing maps SARS-CoV-2 5' capping sites and provides new insights into the structure of sgRNAs.

The furin cleavage site in the SARS-CoV-2 spike protein is required for transmission in ferrets.

Chronic SARS-CoV-2 infection and viral evolution in a hypogammaglobulinaemic individual