Evolution of Bipartite and Segmented Viruses from Monopartite Viruses.

assembly of viruses bipartite viruses evolutionary model segmented viruses

Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
10 05 2023
Historique:
received: 05 04 2023
revised: 30 04 2023
accepted: 05 05 2023
medline: 29 5 2023
pubmed: 27 5 2023
entrez: 27 5 2023
Statut: epublish

Résumé

RNA viruses may be monopartite (all genes on one strand), multipartite (two or more strands packaged separately) or segmented (two or more strands packaged together). In this article, we consider competition between a complete monopartite virus, A, and two defective viruses, D and E, that have complementary genes. We use stochastic models that follow gene translation, RNA replication, virus assembly, and transmission between cells. D and E multiply faster than A when stored in the same host as A or when together in the same host, but they cannot multiply alone. D and E strands are packaged as separate particles unless a mechanism evolves that allows assembly of D + E segmented particles. We show that if defective viruses assemble rapidly into separate particles, the formation of segmented particles is selected against. In this case, D and E spread as parasites of A, and the bipartite D + E combination eliminates A if the transmissibility is high. Alternatively, if defective strands do not assemble rapidly into separate particles, then a mechanism for assembly of segmented particles is selected for. In this case, the segmented virus can eliminate A if transmissibility is high. Conditions of excess protein resources favor bipartite viruses, while conditions of excess RNA resources favor segmented viruses. We study the error threshold behavior that arises when deleterious mutations are introduced. Relative to bipartite and segmented viruses, deleterious mutations favor monopartite viruses. A monopartite virus can give rise to either a bipartite or a segmented virus, but it is unlikely that both will originate from the same virus.

Identifiants

pubmed: 37243221
pii: v15051135
doi: 10.3390/v15051135
pmc: PMC10223652
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Hyunjin Park (H)

Department of Physics and Astronomy, McMaster University, 1280 Main St. West, Hamilton, ON L8M 4S1, Canada.

Saven Denha (S)

Department of Physics and Astronomy, McMaster University, 1280 Main St. West, Hamilton, ON L8M 4S1, Canada.

Paul G Higgs (PG)

Department of Physics and Astronomy, McMaster University, 1280 Main St. West, Hamilton, ON L8M 4S1, Canada.

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