SARS-CoV-2 one year on: evidence for ongoing viral adaptation

Author:

Peacock Thomas P.1ORCID,Penrice-Randal Rebekah2ORCID,Hiscox Julian A.32ORCID,Barclay Wendy S.1ORCID

Affiliation:

1. Department of Infectious Diseases, St Marys Medical School, Imperial College London, UK

2. Institute of Infection, Veterinary and Ecology Sciences, University of Liverpool, UK

3. A*STAR Infectious Diseases Laboratories (A*STAR ID Labs), Agency for Science, Technology and Research (A*STAR), Singapore

Abstract

SARS-CoV-2 is thought to have originated in the human population from a zoonotic spillover event. Infection in humans results in a variety of outcomes ranging from asymptomatic cases to the disease COVID-19, which can have significant morbidity and mortality, with over two million confirmed deaths worldwide as of January 2021. Over a year into the pandemic, sequencing analysis has shown that variants of SARS-CoV-2 are being selected as the virus continues to circulate widely within the human population. The predominant drivers of genetic variation within SARS-CoV-2 are single nucleotide polymorphisms (SNPs) caused by polymerase error, potential host factor driven RNA modification, and insertion/deletions (indels) resulting from the discontinuous nature of viral RNA synthesis. While many mutations represent neutral ‘genetic drift’ or have quickly died out, a subset may be affecting viral traits such as transmissibility, pathogenicity, host range, and antigenicity of the virus. In this review, we summarise the current extent of genetic change in SARS-CoV-2, particularly recently emerging variants of concern, and consider the phenotypic consequences of this viral evolution that may impact the future trajectory of the pandemic.

Funder

Biotechnology and Biological Sciences Research Council

Medical Research Council

U.S. Food and Drug Administration

Wellcome Trust

Publisher

Microbiology Society

Subject

Virology

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