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Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips
Tomato spotted wilt virus (TSWV) is a generalist pathogen with one of the broadest known host ranges among RNA viruses. To understand how TSWV adapts to different hosts, we experimentally passaged viral populations between two alternate hosts, Emilia sochifolia and Datura stramonium, and an obligate...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519039/ https://www.ncbi.nlm.nih.gov/pubmed/32978446 http://dx.doi.org/10.1038/s41598-020-72691-3 |
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author | Ruark-Seward, Casey L. Bonville, Brian Kennedy, George Rasmussen, David A. |
author_facet | Ruark-Seward, Casey L. Bonville, Brian Kennedy, George Rasmussen, David A. |
author_sort | Ruark-Seward, Casey L. |
collection | PubMed |
description | Tomato spotted wilt virus (TSWV) is a generalist pathogen with one of the broadest known host ranges among RNA viruses. To understand how TSWV adapts to different hosts, we experimentally passaged viral populations between two alternate hosts, Emilia sochifolia and Datura stramonium, and an obligate vector in which it also replicates, western flower thrips (Frankliniella occidentalis). Deep sequencing viral populations at multiple time points allowed us to track the evolutionary dynamics of viral populations within and between hosts. High levels of viral genetic diversity were maintained in both plants and thrips between transmission events. Rapid fluctuations in the frequency of amino acid variants indicated strong host-specific selection pressures on proteins involved in viral movement (NSm) and replication (RdRp). While several genetic variants showed opposing fitness effects in different hosts, fitness effects were generally positively correlated between hosts indicating that positive rather than antagonistic pleiotropy is pervasive. These results suggest that high levels of genetic diversity together with the positive pleiotropic effects of mutations have allowed TSWV to rapidly adapt to new hosts and expand its host range. |
format | Online Article Text |
id | pubmed-7519039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75190392020-09-29 Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips Ruark-Seward, Casey L. Bonville, Brian Kennedy, George Rasmussen, David A. Sci Rep Article Tomato spotted wilt virus (TSWV) is a generalist pathogen with one of the broadest known host ranges among RNA viruses. To understand how TSWV adapts to different hosts, we experimentally passaged viral populations between two alternate hosts, Emilia sochifolia and Datura stramonium, and an obligate vector in which it also replicates, western flower thrips (Frankliniella occidentalis). Deep sequencing viral populations at multiple time points allowed us to track the evolutionary dynamics of viral populations within and between hosts. High levels of viral genetic diversity were maintained in both plants and thrips between transmission events. Rapid fluctuations in the frequency of amino acid variants indicated strong host-specific selection pressures on proteins involved in viral movement (NSm) and replication (RdRp). While several genetic variants showed opposing fitness effects in different hosts, fitness effects were generally positively correlated between hosts indicating that positive rather than antagonistic pleiotropy is pervasive. These results suggest that high levels of genetic diversity together with the positive pleiotropic effects of mutations have allowed TSWV to rapidly adapt to new hosts and expand its host range. Nature Publishing Group UK 2020-09-25 /pmc/articles/PMC7519039/ /pubmed/32978446 http://dx.doi.org/10.1038/s41598-020-72691-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ruark-Seward, Casey L. Bonville, Brian Kennedy, George Rasmussen, David A. Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips |
title | Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips |
title_full | Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips |
title_fullStr | Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips |
title_full_unstemmed | Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips |
title_short | Evolutionary dynamics of Tomato spotted wilt virus within and between alternate plant hosts and thrips |
title_sort | evolutionary dynamics of tomato spotted wilt virus within and between alternate plant hosts and thrips |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519039/ https://www.ncbi.nlm.nih.gov/pubmed/32978446 http://dx.doi.org/10.1038/s41598-020-72691-3 |
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