Deep Sequencing Reveals Dual Evolution of SARS‐CoV‐2: Insights Into Defective Genomes From Wuhan‐Hu‐1 Variants to Omicron Subvariants

SARS-CoV-2 has evolved from early variants dominating the first (B.1.5, B.1.1) and second (B.1.177) pandemic waves, which exhibited a higher frequency of minority mutants with deletions leading to Defective Viral Genomes (DVGs) in the spike region near the S1/S2 cleavage site than the Alpha, Beta, and Delta variants. The emergence of Omicron has significantly altered the dominant variant profile, with Omicron subvariants now representing 100% of circulating viruses. To monitor the evolution and adaptation of Omicron in the human population, a deep-sequencing study was performed in RNA samples of BA.1, BA.1.1, BA.2, BA.5, BQ.1.1, XBB.1.5 and BA.2.86 Omicron subvariants. The findings reveal two occurrences of similar evolutionary patterns within SARS-CoV-2 characterized by a shift from a significant to a very low production of DVGs. This event suggests that DVGs might play a role in the virus's spread and adaptation for persistence in infected humans.

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Publication Details

Journal
Journal of Medical Virology
Published
2025-06-30
DOI
https://doi.org/10.1002/jmv.70476
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Deep Sequencing Reveals Dual Evolution of SARS‐CoV‐2: Insights Into Defective Genomes From Wuhan‐Hu‐1 Variants to Omicron Subvariants

Ariadna Rando‐Segura, David Tabernero, María Francesca Cortese, Juliana Esperalba et al.
Journal of Medical Virology
SARS-CoV-2 and COVID-19 Research
article

Deep Sequencing Reveals Dual Evolution of SARS‐CoV‐2: Insights Into Defective Genomes From Wuhan‐Hu‐1 Variants to Omicron Subvariants

Ariadna Rando‐Segura, David Tabernero, María Francesca Cortese, Juliana Esperalba, Damir García‐Cehic, Sergi Colomer‐Castell, Narcı́s Saubi, Renate W. Hakze‐van der Honing, María Piñana, Alejandra Gónzalez‐Sánchez, Josep Quer, Francisco Rodríguez‐Frias, Cristina Andrés, Juan Ignacio Esteban, Andrés Antón, Andries A. Kampfraath, Roser Ferrer, Joaquím Segalés, Júlia Vergara‐Alert, Carolina Campos, Marta Ibañez‐Lligoña, Josep Gregori, Tomàs Pumarola, Wim H. M. van der Poel
article en

Abstract

SARS-CoV-2 has evolved from early variants dominating the first (B.1.5, B.1.1) and second (B.1.177) pandemic waves, which exhibited a higher frequency of minority mutants with deletions leading to Defective Viral Genomes (DVGs) in the spike region near the S1/S2 cleavage site than the Alpha, Beta, and Delta variants. The emergence of Omicron has significantly altered the dominant variant profile, with Omicron subvariants now representing 100% of circulating viruses. To monitor the evolution and adaptation of Omicron in the human population, a deep-sequencing study was performed in RNA samples of BA.1, BA.1.1, BA.2, BA.5, BQ.1.1, XBB.1.5 and BA.2.86 Omicron subvariants. The findings reveal two occurrences of similar evolutionary patterns within SARS-CoV-2 characterized by a shift from a significant to a very low production of DVGs. This event suggests that DVGs might play a role in the virus's spread and adaptation for persistence in infected humans.

Journal of Medical VirologyVol. 97(7)
Universitat Autònoma de Barcelona (ES), Instituto de Salud Carlos III (ES), Universitat Internacional de Catalunya (ES), Centre de Recerca en Sanitat Animal (ES), Vall d'Hebron Institut de Recerca (ES), Vall d'Hebron Hospital Universitari (ES), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (ES), Wageningen University & Research (NL), University of Cincinnati Medical Center (US)
European Commission, Centro para el Desarrollo Tecnológico Industrial, Ministerio de Economía y Competitividad, Ministerio de Ciencia e Innovación, Fundació Institut de Recerca Hospital Universitari Vall d’Hebron, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona, Instituto de Salud Carlos III, European Regional Development Fund, Agencia Estatal de Investigación
Good health and well-being
Openalex Percentile: Top 81%
SARS-CoV-2 and COVID-19 Research
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