Mapping the Evolutionary Space of SARS-CoV-2 Variants to Anticipate Emergence of Subvariants Resistant to COVID-19 Therapeutics.


Journal

PLoS computational biology
ISSN: 1553-7358
Titre abrégé: PLoS Comput Biol
Pays: United States
ID NLM: 101238922

Informations de publication

Date de publication:
10 Jun 2024
Historique:
received: 06 07 2023
accepted: 30 05 2024
medline: 10 6 2024
pubmed: 10 6 2024
entrez: 10 6 2024
Statut: aheadofprint

Résumé

New sublineages of SARS-CoV-2 variants-of-concern (VOCs) continuously emerge with mutations in the spike glycoprotein. In most cases, the sublineage-defining mutations vary between the VOCs. It is unclear whether these differences reflect lineage-specific likelihoods for mutations at each spike position or the stochastic nature of their appearance. Here we show that SARS-CoV-2 lineages have distinct evolutionary spaces (a probabilistic definition of the sequence states that can be occupied by expanding virus subpopulations). This space can be accurately inferred from the patterns of amino acid variability at the whole-protein level. Robust networks of co-variable sites identify the highest-likelihood mutations in new VOC sublineages and predict remarkably well the emergence of subvariants with resistance mutations to COVID-19 therapeutics. Our studies reveal the contribution of low frequency variant patterns at heterologous sites across the protein to accurate prediction of the changes at each position of interest.

Identifiants

pubmed: 38857308
doi: 10.1371/journal.pcbi.1012215
pii: PCOMPBIOL-D-23-01068
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1012215

Informations de copyright

Copyright: © 2024 Rojas Chávez et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Roberth Anthony Rojas Chávez (RA)

Department of Microbiology and Immunology, The University of Iowa, Iowa City, Iowa, United States of America.

Mohammad Fili (M)

Department of Industrial and Manufacturing Systems Engineering, Iowa State University, Ames, Iowa, United States of America.

Changze Han (C)

Department of Microbiology and Immunology, The University of Iowa, Iowa City, Iowa, United States of America.

Syed A Rahman (SA)

Center for Systems Immunology, Departments of Immunology and Computational & Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.

Isaiah G L Bicar (IGL)

Department of Microbiology and Immunology, The University of Iowa, Iowa City, Iowa, United States of America.

Sullivan Gregory (S)

Department of Microbiology and Immunology, The University of Iowa, Iowa City, Iowa, United States of America.

Annika Helverson (A)

Department of Biostatistics, College of Public Health, The University of Iowa, Iowa City, Iowa, United States of America.

Guiping Hu (G)

Department of Industrial and Manufacturing Systems Engineering, Iowa State University, Ames, Iowa, United States of America.

Benjamin W Darbro (BW)

Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States of America.

Jishnu Das (J)

Center for Systems Immunology, Departments of Immunology and Computational & Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.

Grant D Brown (GD)

Department of Biostatistics, College of Public Health, The University of Iowa, Iowa City, Iowa, United States of America.

Hillel Haim (H)

Department of Microbiology and Immunology, The University of Iowa, Iowa City, Iowa, United States of America.

Classifications MeSH