Tracking SARS-CoV-2 Mutations & Variants Through the COG-UK-Mutation Explorer

Author:

Wright Derek W1,Harvey William T1,Hughes Joseph1ORCID,Cox MacGregor2,Peacock Thomas P3,Colquhoun Rachel4ORCID,Jackson Ben4ORCID,Orton Richard1ORCID,Nielsen Morten5ORCID,Hsu Nienyun Sharon6,Harrison Ewan M278,de Silva Thushan I6,Rambaut Andrew4ORCID,Peacock Sharon J2ORCID,Robertson David L1ORCID,Carabelli Alessandro M2ORCID

Affiliation:

1. MRC-University of Glasgow Centre for Virus Research, University of Glasgow, Glasgow, UK

2. Department of Medicine, University of Cambridge, Cambridge, UK

3. Department of Infectious Disease, St Mary’s Medical School, Imperial College London, UK

4. Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK

5. Universidad Nacional de San Martin, Argentina

6. The Florey Institute for Host-Pathogen Interactions and Department of Infection, Immunity and Cardiovascular Disease, Medical School, University of Sheffield, Sheffield, UK

7. Wellcome Sanger Institute, Hinxton, UK

8. Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK

Abstract

Abstract COG-UK Mutation Explorer (COG-UK-ME, https://sars2.cvr.gla.ac.uk/cog-uk/ - Last Accessed date 16/03/22) is a web resource that displays knowledge and analyses on SARS-CoV-2 virus genome mutations and variants circulating in the UK, with a focus on the observed amino acid replacements that have an antigenic role in the context of the human humoral and cellular immune response. This analysis is based on more than 2 million genome sequences (as of March 2022) for UK SARS-CoV-2 data held in the CLIMB-COVID centralised data environment. COG-UK-ME curates these data and displays analyses that are cross-referenced to experimental data collated from the primary literature. The aim is to track mutations of immunological importance that are accumulating in current variants of concern and variants of interest that could alter the neutralising activity of monoclonal antibodies (mAbs), convalescent sera and vaccines. Changes in epitopes recognised by T cells, including those where reduced T cell binding has been demonstrated, are reported. Mutations that have been shown to confer SARS-CoV-2 resistance to antiviral drugs are also included. Using visualisation tools, COG-UK-ME also allows users to identify the emergence of variants carrying mutations that could decrease the neutralising activity of both mAbs present in therapeutic cocktails, e.g., Ronapreve. COG-UK-ME tracks changes in frequency of combination of mutations and brings together curated literature on the impact of those mutations on various functional aspects of the virus and therapeutics. Given SARS-CoV-2 unpredictable nature as exemplified by yet another variant of concern, Omicron, continued surveillance of SARS-CoV-2 remains imperative to monitor virus evolution linked to the efficacy of therapeutics.

Funder

Wellcome Trust

Medical Research Council (MRC) part of UK Research & Innovation (UKRI), the National Institute of Health Research

G2P-UK National Virology Consortium

Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

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