SARS-CoV-2 genetic diversity and stability in the presence of neutralising antibodies and antivirals
Lead Research Organisation:
University of Bristol
Department Name: Cellular and Molecular Medicine
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.
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.
Organisations
Publications
Peacock TP
(2021)
The furin cleavage site in the SARS-CoV-2 spike protein is required for transmission in ferrets.
in Nature microbiology
Ugolini C
(2022)
Nanopore ReCappable sequencing maps SARS-CoV-2 5' capping sites and provides new insights into the structure of sgRNAs.
in Nucleic acids research
Description | We learned how to work safely with highy dangerous coronaviruses. |
Exploitation Route | We took it forward by improving our skills to work on SARS-CoV-2. |
Sectors | Healthcare |
Description | Press artcles, radio and television interviews |
Form Of Engagement Activity | A press release, press conference or response to a media enquiry/interview |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Public/other audiences |
Results and Impact | I have been interviewed extensively about my work on SARS-CoV-2 |
Year(s) Of Engagement Activity | 2020 |