Analysis of 6.4 million SARS-CoV-2 genomes identifies mutations associated with fitness

Fritz Obermeyer(Broad Institute), Martin Jankowiak(Broad Institute), Nikolaos Barkas(Broad Institute), S. F. Schaffner(Broad Institute), Jesse D. Pyle(Broad Institute), Lonya Yurkovetskiy(University of Massachusetts Chan Medical School), Matteo Bosso(University of Massachusetts Chan Medical School), Daniel Park(Broad Institute), Mehrtash Babadi(Broad Institute), Bronwyn MacInnis(Broad Institute), Jeremy Luban(Broad Institute), Pardis C. Sabeti(Broad Institute), Jacob E. Lemieux(Broad Institute)
medRxiv
September 13, 2021
Cited by 60Open Access
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Abstract

Abstract Repeated emergence of SARS-CoV-2 variants with increased fitness necessitates rapid detection and characterization of new lineages. To address this need, we developed PyR 0 , a hierarchical Bayesian multinomial logistic regression model that infers relative prevalence of all viral lineages across geographic regions, detects lineages increasing in prevalence, and identifies mutations relevant to fitness. Applying PyR 0 to all publicly available SARS-CoV-2 genomes, we identify numerous substitutions that increase fitness, including previously identified spike mutations and many non-spike mutations within the nucleocapsid and nonstructural proteins. PyR 0 forecasts growth of new lineages from their mutational profile, identifies viral lineages of concern as they emerge, and prioritizes mutations of biological and public health concern for functional characterization. One Sentence summary A Bayesian hierarchical model of all SARS-CoV-2 viral genomes predicts lineage fitness and identifies associated mutations.


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