Cargando…

Evolution of Bipartite and Segmented Viruses from Monopartite Viruses

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 compl...

Descripción completa

Detalles Bibliográficos
Autores principales: Park, Hyunjin, Denha, Saven, Higgs, Paul G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223652/
https://www.ncbi.nlm.nih.gov/pubmed/37243221
http://dx.doi.org/10.3390/v15051135
_version_ 1785049992870756352
author Park, Hyunjin
Denha, Saven
Higgs, Paul G.
author_facet Park, Hyunjin
Denha, Saven
Higgs, Paul G.
author_sort Park, Hyunjin
collection PubMed
description 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.
format Online
Article
Text
id pubmed-10223652
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-102236522023-05-28 Evolution of Bipartite and Segmented Viruses from Monopartite Viruses Park, Hyunjin Denha, Saven Higgs, Paul G. Viruses Article 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. MDPI 2023-05-10 /pmc/articles/PMC10223652/ /pubmed/37243221 http://dx.doi.org/10.3390/v15051135 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Park, Hyunjin
Denha, Saven
Higgs, Paul G.
Evolution of Bipartite and Segmented Viruses from Monopartite Viruses
title Evolution of Bipartite and Segmented Viruses from Monopartite Viruses
title_full Evolution of Bipartite and Segmented Viruses from Monopartite Viruses
title_fullStr Evolution of Bipartite and Segmented Viruses from Monopartite Viruses
title_full_unstemmed Evolution of Bipartite and Segmented Viruses from Monopartite Viruses
title_short Evolution of Bipartite and Segmented Viruses from Monopartite Viruses
title_sort evolution of bipartite and segmented viruses from monopartite viruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223652/
https://www.ncbi.nlm.nih.gov/pubmed/37243221
http://dx.doi.org/10.3390/v15051135
work_keys_str_mv AT parkhyunjin evolutionofbipartiteandsegmentedvirusesfrommonopartiteviruses
AT denhasaven evolutionofbipartiteandsegmentedvirusesfrommonopartiteviruses
AT higgspaulg evolutionofbipartiteandsegmentedvirusesfrommonopartiteviruses