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

Wright, Derek W., Harvey, William T., Hughes, Joseph, Cox, MacGregor, Peacock, Thomas P., Colquhoun, Rachel, Jackson, Ben, Orton, Richard, Nielsen, Morten, Hsu, Nienyun Sharon, Harrison, Ewan M., de Silva, Thushan I., Rambaut, Andrew, Peacock, Sharon J., Robertson, David L., Carabelli, Alessandro M., The COVID-19 Genomics UK (COG-UK) Consortium, , Bashton, Matthew, Smith, Darren, Young, Greg, Nelson, Andrew and McCann, Clare (2022) Tracking SARS-CoV-2 Mutations & Variants Through the COG-UK-Mutation Explorer. Virus Evolution, 8 (1). veac023. ISSN 2057-1577

[img]
Preview
Text
veac023.pdf - Published Version
Available under License Creative Commons Attribution 4.0.

Download (3MB) | Preview
Official URL: https://doi.org/10.1093/ve/veac023

Abstract

COG-UK Mutation Explorer (COG-UK-ME, https://sars2.cvr.gla.ac.uk/cog-uk/—last accessed date 16 March 2022) 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 the frequency of combinations of mutations and brings together the curated literature on the impact of those mutations on various functional aspects of the virus and therapeutics. Given the unpredictable nature of SARS-CoV-2 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.

Item Type: Article
Additional Information: Matthew Bashton, Andrew Nelson, Darren Smith, Greg Young and Clare McCann are member of the COVID-19 Genomics UK (COG-UK) Consortium.
Uncontrolled Keywords: SARS-CoV-2, COVID-19, virus, spike, protein structure, antibody escape, antigenic variation, mutation, amino acid replacements, variants of concern, evasion, resistance, fitness, evolution
Subjects: C700 Molecular Biology, Biophysics and Biochemistry
Depositing User: Elena Carlaw
Date Deposited: 21 Jul 2022 16:59
Last Modified: 21 Jul 2022 17:00
URI: http://nrl.northumbria.ac.uk/id/eprint/49594

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics