Ongoing global and regional adaptive evolution of SARS-CoV-2.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
20 07 2021
Historique:
entrez: 22 7 2021
pubmed: 23 7 2021
medline: 7 8 2021
Statut: ppublish

Résumé

Understanding the trends in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) evolution is paramount to control the COVID-19 pandemic. We analyzed more than 300,000 high-quality genome sequences of SARS-CoV-2 variants available as of January 2021. The results show that the ongoing evolution of SARS-CoV-2 during the pandemic is characterized primarily by purifying selection, but a small set of sites appear to evolve under positive selection. The receptor-binding domain of the spike protein and the region of the nucleocapsid protein associated with nuclear localization signals (NLS) are enriched with positively selected amino acid replacements. These replacements form a strongly connected network of apparent epistatic interactions and are signatures of major partitions in the SARS-CoV-2 phylogeny. Virus diversity within each geographic region has been steadily growing for the entirety of the pandemic, but analysis of the phylogenetic distances between pairs of regions reveals four distinct periods based on global partitioning of the tree and the emergence of key mutations. The initial period of rapid diversification into region-specific phylogenies that ended in February 2020 was followed by a major extinction event and global homogenization concomitant with the spread of D614G in the spike protein, ending in March 2020. The NLS-associated variants across multiple partitions rose to global prominence in March to July, during a period of stasis in terms of interregional diversity. Finally, beginning in July 2020, multiple mutations, some of which have since been demonstrated to enable antibody evasion, began to emerge associated with ongoing regional diversification, which might be indicative of speciation.

Identifiants

pubmed: 34292871
pii: 2104241118
doi: 10.1073/pnas.2104241118
pmc: PMC8307621
pii:
doi:

Substances chimiques

Coronavirus Nucleocapsid Proteins 0
Nuclear Localization Signals 0
Phosphoproteins 0
Spike Glycoprotein, Coronavirus 0
nucleocapsid phosphoprotein, SARS-CoV-2 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Intramural NIH HHS
ID : 1DP1 HL141201
Pays : United States
Organisme : Howard Hughes Medical Institute
Pays : United States
Organisme : NHLBI NIH HHS
ID : DP1 HL141201
Pays : United States
Organisme : Intramural NIH HHS
ID : 1R01 HG009761
Pays : United States
Organisme : NHGRI NIH HHS
ID : R01 HG009761
Pays : United States
Organisme : NHGRI NIH HHS
ID : RM1 HG006193
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

Copyright © 2021 the Author(s). Published by PNAS.

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Nash D Rochman (ND)

National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894; nash.rochman@nih.gov zhang@broadinstitute.org Koonin@ncbi.nlm.nih.gov.

Yuri I Wolf (YI)

National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894.

Guilhem Faure (G)

Broad Institute of MIT and Harvard, Cambridge, MA 02142.

Pascal Mutz (P)

National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894.

Feng Zhang (F)

Broad Institute of MIT and Harvard, Cambridge, MA 02142; nash.rochman@nih.gov zhang@broadinstitute.org Koonin@ncbi.nlm.nih.gov.
HHMI, Massachusetts Institute of Technology, Cambridge, MA 02139.
McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA 02139.
Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139.
Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.

Eugene V Koonin (EV)

National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894; nash.rochman@nih.gov zhang@broadinstitute.org Koonin@ncbi.nlm.nih.gov.

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Classifications MeSH