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Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution
Microbial symbionts can modulate host interactions with biotic and abiotic factors. Such interactions may affect the evolutionary trajectories of both host and symbiont. Wolbachia protects Drosophila melanogaster against several viral infections and the strength of the protection varies between vari...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042464/ https://www.ncbi.nlm.nih.gov/pubmed/27684942 http://dx.doi.org/10.1371/journal.pgen.1006297 |
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author | Faria, Vitor G. Martins, Nelson E. Magalhães, Sara Paulo, Tânia F. Nolte, Viola Schlötterer, Christian Sucena, Élio Teixeira, Luis |
author_facet | Faria, Vitor G. Martins, Nelson E. Magalhães, Sara Paulo, Tânia F. Nolte, Viola Schlötterer, Christian Sucena, Élio Teixeira, Luis |
author_sort | Faria, Vitor G. |
collection | PubMed |
description | Microbial symbionts can modulate host interactions with biotic and abiotic factors. Such interactions may affect the evolutionary trajectories of both host and symbiont. Wolbachia protects Drosophila melanogaster against several viral infections and the strength of the protection varies between variants of this endosymbiont. Since Wolbachia is maternally transmitted, its fitness depends on the fitness of its host. Therefore, Wolbachia populations may be under selection when Drosophila is subjected to viral infection. Here we show that in D. melanogaster populations selected for increased survival upon infection with Drosophila C virus there is a strong selection coefficient for specific Wolbachia variants, leading to their fixation. Flies carrying these selected Wolbachia variants have higher survival and fertility upon viral infection when compared to flies with the other variants. These findings demonstrate how the interaction of a host with pathogens shapes the genetic composition of symbiont populations. Furthermore, host adaptation can result from the evolution of its symbionts, with host and symbiont functioning as a single evolutionary unit. |
format | Online Article Text |
id | pubmed-5042464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50424642016-10-27 Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution Faria, Vitor G. Martins, Nelson E. Magalhães, Sara Paulo, Tânia F. Nolte, Viola Schlötterer, Christian Sucena, Élio Teixeira, Luis PLoS Genet Research Article Microbial symbionts can modulate host interactions with biotic and abiotic factors. Such interactions may affect the evolutionary trajectories of both host and symbiont. Wolbachia protects Drosophila melanogaster against several viral infections and the strength of the protection varies between variants of this endosymbiont. Since Wolbachia is maternally transmitted, its fitness depends on the fitness of its host. Therefore, Wolbachia populations may be under selection when Drosophila is subjected to viral infection. Here we show that in D. melanogaster populations selected for increased survival upon infection with Drosophila C virus there is a strong selection coefficient for specific Wolbachia variants, leading to their fixation. Flies carrying these selected Wolbachia variants have higher survival and fertility upon viral infection when compared to flies with the other variants. These findings demonstrate how the interaction of a host with pathogens shapes the genetic composition of symbiont populations. Furthermore, host adaptation can result from the evolution of its symbionts, with host and symbiont functioning as a single evolutionary unit. Public Library of Science 2016-09-29 /pmc/articles/PMC5042464/ /pubmed/27684942 http://dx.doi.org/10.1371/journal.pgen.1006297 Text en © 2016 Faria et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Faria, Vitor G. Martins, Nelson E. Magalhães, Sara Paulo, Tânia F. Nolte, Viola Schlötterer, Christian Sucena, Élio Teixeira, Luis Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution |
title | Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution |
title_full | Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution |
title_fullStr | Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution |
title_full_unstemmed | Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution |
title_short | Drosophila Adaptation to Viral Infection through Defensive Symbiont Evolution |
title_sort | drosophila adaptation to viral infection through defensive symbiont evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042464/ https://www.ncbi.nlm.nih.gov/pubmed/27684942 http://dx.doi.org/10.1371/journal.pgen.1006297 |
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