Cooccurrence of N501Y, P681R and other key mutations in SARS-CoV-2 Spike

Author:

Lee Carol,Mangalaganesh Shruthi,Wilson Laurence O.W.,Kuiper Michael J.,Drew Trevor W.,Vasan Seshadri S.ORCID

Abstract

AbstractAnalysis of circa 4.2 million severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome sequences on ‘Global Initiative on Sharing All Influenza Data (GISAID)’ shows the spike mutations ‘N501Y’ (common to Alpha, Beta, Gamma, Omicron variants) and ‘P681R’ (central to Delta variant’s spread) have cooccurred 3,678 times between 17 October 2020 and 1 November 2021. In contrast, the N501Y+P681H combination is present in Alpha and Omicron variants and circa 1.1 million entries. Two-thirds of the 3,678 cooccurrences were in France, Turkey or US (East Coast), and the rest across 62 other countries. 55.5% and 4.6% of the cooccurrences were Alpha’s Q.4 and Gamma’s P.1.8 sub-lineages acquiring P681R; 10.7% and 3.8% were Delta’s B.1.617.2 lineage and AY.33 sub-lineage acquiring N501Y; remaining 10.2% were in other variants. Despite the selective advantages individually conferred by N501Y and P681R, the N501Y+P681R combination counterintuitively didn’t outcompete other variants in every instance. Although a relief to worldwide public health efforts, in vitro and in vivo studies are urgently required in the absence of a strong in silico explanation for this phenomenon. This study demonstrates a pipeline to analyse combinations of key mutations from public domain information in a systematic manner and provide early warnings of spread.

Publisher

Cold Spring Harbor Laboratory

Reference47 articles.

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