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The emergence and ongoing convergent evolution of the SARS-CoV-2 N501Y lineages.

Authors :
Martin, Darren P.
Weaver, Steven
Tegally, Houriiyah
San, James Emmanuel
Shank, Stephen D.
Wilkinson, Eduan
Lucaci, Alexander G.
Giandhari, Jennifer
Naidoo, Sureshnee
Pillay, Yeshnee
Singh, Lavanya
Lessells, Richard J.
Gupta, Ravindra K.
Wertheim, Joel O.
Nekturenko, Anton
Murrell, Ben
Harkins, Gordon W.
Lemey, Philippe
MacLean, Oscar A.
Robertson, David L.
Source :
Cell. Sep2021, Vol. 184 Issue 20, p5189-5189. 1p.
Publication Year :
2021

Abstract

The independent emergence late in 2020 of the B.1.1.7, B.1.351, and P.1 lineages of SARS-CoV-2 prompted renewed concerns about the evolutionary capacity of this virus to overcome public health interventions and rising population immunity. Here, by examining patterns of synonymous and non-synonymous mutations that have accumulated in SARS-CoV-2 genomes since the pandemic began, we find that the emergence of these three "501Y lineages" coincided with a major global shift in the selective forces acting on various SARS-CoV-2 genes. Following their emergence, the adaptive evolution of 501Y lineage viruses has involved repeated selectively favored convergent mutations at 35 genome sites, mutations we refer to as the 501Y meta-signature. The ongoing convergence of viruses in many other lineages on this meta-signature suggests that it includes multiple mutation combinations capable of promoting the persistence of diverse SARS-CoV-2 lineages in the face of mounting host immune recognition. [Display omitted] • Detected a major global shift in the SARS-CoV-2 selective landscape in late 2020 • Identified ongoing convergent evolution between the alpha, beta, and gamma lineages • Defined the mutational meta-signature upon which these lineages are converging An analysis of synonymous and non-synonymous mutations in SARS-CoV-2 genomes since the inception of the COVID-19 pandemic provides insights into the emergence of a convergent mutational signature in the 501Y lineage (alpha, beta, and gamma variants) that is also likely present in other lineages that impacts host immune recognition. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00928674
Volume :
184
Issue :
20
Database :
Academic Search Index
Journal :
Cell
Publication Type :
Academic Journal
Accession number :
152794159
Full Text :
https://doi.org/10.1016/j.cell.2021.09.003