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SARS-CoV-2 mutant spectra as variant of concern nurseries: endless variation?

Authors :
Martínez-González, Brenda
Eugenia Soria, María
Mínguez, Pablo
Lorenzo-Redondo, Ramón
Salar-Vidal, Llanos
López-García, Alberto
Esteban-Muñoz, Mario
Durán-Pastor, Antoni
Somovilla, Pilar
García-Crespo, Carlos
de Ávila, Ana Isabel
Gómez, Jordi
Esteban, Jaime
Fernández-Roblas, Ricardo
Gadea, Ignacio
Domingo, Esteban
Perales, Celia
Source :
Frontiers in Microbiology; 2024, p1-13, 13p
Publication Year :
2024

Abstract

Introduction: SARS-CoV-2 isolates of a given clade may contain low frequency genomes that encode amino acids or deletions which are typical of a different clade. Methods: Here we use high resolution ultra-deep sequencing to analyze SARSCoV-2 mutant spectra. Results: In 6 out of 11 SARS-CoV-2 isolates from COVID-19 patients, the mutant spectrum of the spike (S)-coding region included two or more amino acids or deletions, that correspond to discordant viral clades. A similar observation is reported for laboratory populations of SARS-CoV-2 USA-WA1/2020, following a cell culture infection in the presence of remdesivir, ribavirin or their combinations. Moreover, some of the clade-discordant genome residues are found in the same haplotype within an amplicon. Discussion: We evaluate possible interpretations of these findings, and reviewed precedents for rapid selection of genomes with multiple mutations in RNA viruses. These considerations suggest that intra-host evolution may be sufficient to generate minority sequences which are closely related to sequences typical of other clades. The results provide a model for the origin of variants of concern during epidemic spread-in particular Omicron lineages-that does not require prolonged infection, involvement of immunocompromised individuals, or participation of intermediate, non-human hosts. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1664302X
Database :
Complementary Index
Journal :
Frontiers in Microbiology
Publication Type :
Academic Journal
Accession number :
176324188
Full Text :
https://doi.org/10.3389/fmicb.2024.1358258