Affiliation:
1. IHU Méditerranée Infection Marseille France
2. Aix‐Marseille Université., Institut de Recherche pour le Développement (IRD), Microbes Evolution Phylogeny and Infections (MEPHI) Marseille France
3. Assistance Publique‐Hôpitaux de Marseille (AP‐HM) Marseille France
4. INSERM UMR_S 1072, Aix‐Marseille Université Marseille France
5. Department of Biological Sciences Centre National de la Recherche 16 Scientifique (CNRS)‐SNC5039 Marseille France
Abstract
AbstractThe tremendous majority of RNA genomes from pathogenic viruses analyzed and deposited in databases are consensus or “democratic” genomes. They represent the genomes most frequently found in the clinical samples of patients but do not account for the huge genetic diversity of coexisting genomes, which is better described as quasispecies. A viral quasispecies is defined as the dynamic distribution of nonidentical but closely related mutants, variants, recombinant, or reassortant viral genomes. Viral quasispecies have collective behavior and dynamics and are the subject of internal interactions that comprise interference, complementation, or cooperation. In the setting of SARS‐CoV‐2 infection, intrahost SARS‐CoV‐2 genetic diversity was recently notably reported for immunocompromised, chronically infected patients, for patients treated with monoclonal antibodies targeting the viral spike protein, and for different body compartments of a single patient. A question that deserves attention is whether such diversity is generated postinfection from a clonal genome in response to selection pressure or is already present at the time of infection as a quasispecies. In the present review, we summarize the data supporting that hosts are infected by a “wild bunch” of viruses rather than by multiple virions sharing the same genome. Each virion in the “wild bunch” may have different virulence and tissue tropisms. As the number of viruses replicated during host infections is huge, a viral quasispecies at any time of infection is wide and is also influenced by host‐specific selection pressure after infection, which accounts for the difficulty in deciphering and predicting the appearance of more fit variants and the evolution of epidemics of novel RNA viruses.
Funder
Agence Nationale de la Recherche
Subject
Infectious Diseases,Virology
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献