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Parallels between experimental and natural evolution of legume symbionts

The emergence of symbiotic interactions has been studied using population genomics in nature and experimental evolution in the laboratory, but the parallels between these processes remain unknown. Here we compare the emergence of rhizobia after the horizontal transfer of a symbiotic plasmid in natur...

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Autores principales: Clerissi, Camille, Touchon, Marie, Capela, Delphine, Tang, Mingxing, Cruveiller, Stéphane, Genthon, Clémence, Lopez-Roques, Céline, Parker, Matthew A., Moulin, Lionel, Masson-Boivin, Catherine, Rocha, Eduardo P. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995829/
https://www.ncbi.nlm.nih.gov/pubmed/29891837
http://dx.doi.org/10.1038/s41467-018-04778-5
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author Clerissi, Camille
Touchon, Marie
Capela, Delphine
Tang, Mingxing
Cruveiller, Stéphane
Genthon, Clémence
Lopez-Roques, Céline
Parker, Matthew A.
Moulin, Lionel
Masson-Boivin, Catherine
Rocha, Eduardo P. C.
author_facet Clerissi, Camille
Touchon, Marie
Capela, Delphine
Tang, Mingxing
Cruveiller, Stéphane
Genthon, Clémence
Lopez-Roques, Céline
Parker, Matthew A.
Moulin, Lionel
Masson-Boivin, Catherine
Rocha, Eduardo P. C.
author_sort Clerissi, Camille
collection PubMed
description The emergence of symbiotic interactions has been studied using population genomics in nature and experimental evolution in the laboratory, but the parallels between these processes remain unknown. Here we compare the emergence of rhizobia after the horizontal transfer of a symbiotic plasmid in natural populations of Cupriavidus taiwanensis, over 10 MY ago, with the experimental evolution of symbiotic Ralstonia solanacearum for a few hundred generations. In spite of major differences in terms of time span, environment, genetic background, and phenotypic achievement, both processes resulted in rapid genetic diversification dominated by purifying selection. We observe no adaptation in the plasmid carrying the genes responsible for the ecological transition. Instead, adaptation was associated with positive selection in a set of genes that led to the co-option of the same quorum-sensing system in both processes. Our results provide evidence for similarities in experimental and natural evolutionary transitions and highlight the potential of comparisons between both processes to understand symbiogenesis.
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spelling pubmed-59958292018-06-13 Parallels between experimental and natural evolution of legume symbionts Clerissi, Camille Touchon, Marie Capela, Delphine Tang, Mingxing Cruveiller, Stéphane Genthon, Clémence Lopez-Roques, Céline Parker, Matthew A. Moulin, Lionel Masson-Boivin, Catherine Rocha, Eduardo P. C. Nat Commun Article The emergence of symbiotic interactions has been studied using population genomics in nature and experimental evolution in the laboratory, but the parallels between these processes remain unknown. Here we compare the emergence of rhizobia after the horizontal transfer of a symbiotic plasmid in natural populations of Cupriavidus taiwanensis, over 10 MY ago, with the experimental evolution of symbiotic Ralstonia solanacearum for a few hundred generations. In spite of major differences in terms of time span, environment, genetic background, and phenotypic achievement, both processes resulted in rapid genetic diversification dominated by purifying selection. We observe no adaptation in the plasmid carrying the genes responsible for the ecological transition. Instead, adaptation was associated with positive selection in a set of genes that led to the co-option of the same quorum-sensing system in both processes. Our results provide evidence for similarities in experimental and natural evolutionary transitions and highlight the potential of comparisons between both processes to understand symbiogenesis. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995829/ /pubmed/29891837 http://dx.doi.org/10.1038/s41467-018-04778-5 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Clerissi, Camille
Touchon, Marie
Capela, Delphine
Tang, Mingxing
Cruveiller, Stéphane
Genthon, Clémence
Lopez-Roques, Céline
Parker, Matthew A.
Moulin, Lionel
Masson-Boivin, Catherine
Rocha, Eduardo P. C.
Parallels between experimental and natural evolution of legume symbionts
title Parallels between experimental and natural evolution of legume symbionts
title_full Parallels between experimental and natural evolution of legume symbionts
title_fullStr Parallels between experimental and natural evolution of legume symbionts
title_full_unstemmed Parallels between experimental and natural evolution of legume symbionts
title_short Parallels between experimental and natural evolution of legume symbionts
title_sort parallels between experimental and natural evolution of legume symbionts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995829/
https://www.ncbi.nlm.nih.gov/pubmed/29891837
http://dx.doi.org/10.1038/s41467-018-04778-5
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