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Experimental Evolution of Legume Symbionts: What Have We Learnt?

Rhizobia, the nitrogen-fixing symbionts of legumes, are polyphyletic bacteria distributed in many alpha- and beta-proteobacterial genera. They likely emerged and diversified through independent horizontal transfers of key symbiotic genes. To replay the evolution of a new rhizobium genus under labora...

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Autores principales: Doin de Moura, Ginaini Grazielli, Remigi, Philippe, Masson-Boivin, Catherine, Capela, Delphine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141107/
https://www.ncbi.nlm.nih.gov/pubmed/32210028
http://dx.doi.org/10.3390/genes11030339
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author Doin de Moura, Ginaini Grazielli
Remigi, Philippe
Masson-Boivin, Catherine
Capela, Delphine
author_facet Doin de Moura, Ginaini Grazielli
Remigi, Philippe
Masson-Boivin, Catherine
Capela, Delphine
author_sort Doin de Moura, Ginaini Grazielli
collection PubMed
description Rhizobia, the nitrogen-fixing symbionts of legumes, are polyphyletic bacteria distributed in many alpha- and beta-proteobacterial genera. They likely emerged and diversified through independent horizontal transfers of key symbiotic genes. To replay the evolution of a new rhizobium genus under laboratory conditions, the symbiotic plasmid of Cupriavidus taiwanensis was introduced in the plant pathogen Ralstonia solanacearum, and the generated proto-rhizobium was submitted to repeated inoculations to the C. taiwanensis host, Mimosa pudica L. This experiment validated a two-step evolutionary scenario of key symbiotic gene acquisition followed by genome remodeling under plant selection. Nodulation and nodule cell infection were obtained and optimized mainly via the rewiring of regulatory circuits of the recipient bacterium. Symbiotic adaptation was shown to be accelerated by the activity of a mutagenesis cassette conserved in most rhizobia. Investigating mutated genes led us to identify new components of R. solanacearum virulence and C. taiwanensis symbiosis. Nitrogen fixation was not acquired in our short experiment. However, we showed that post-infection sanctions allowed the increase in frequency of nitrogen-fixing variants among a non-fixing population in the M. pudica–C. taiwanensis system and likely allowed the spread of this trait in natura. Experimental evolution thus provided new insights into rhizobium biology and evolution.
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spelling pubmed-71411072020-04-10 Experimental Evolution of Legume Symbionts: What Have We Learnt? Doin de Moura, Ginaini Grazielli Remigi, Philippe Masson-Boivin, Catherine Capela, Delphine Genes (Basel) Review Rhizobia, the nitrogen-fixing symbionts of legumes, are polyphyletic bacteria distributed in many alpha- and beta-proteobacterial genera. They likely emerged and diversified through independent horizontal transfers of key symbiotic genes. To replay the evolution of a new rhizobium genus under laboratory conditions, the symbiotic plasmid of Cupriavidus taiwanensis was introduced in the plant pathogen Ralstonia solanacearum, and the generated proto-rhizobium was submitted to repeated inoculations to the C. taiwanensis host, Mimosa pudica L. This experiment validated a two-step evolutionary scenario of key symbiotic gene acquisition followed by genome remodeling under plant selection. Nodulation and nodule cell infection were obtained and optimized mainly via the rewiring of regulatory circuits of the recipient bacterium. Symbiotic adaptation was shown to be accelerated by the activity of a mutagenesis cassette conserved in most rhizobia. Investigating mutated genes led us to identify new components of R. solanacearum virulence and C. taiwanensis symbiosis. Nitrogen fixation was not acquired in our short experiment. However, we showed that post-infection sanctions allowed the increase in frequency of nitrogen-fixing variants among a non-fixing population in the M. pudica–C. taiwanensis system and likely allowed the spread of this trait in natura. Experimental evolution thus provided new insights into rhizobium biology and evolution. MDPI 2020-03-23 /pmc/articles/PMC7141107/ /pubmed/32210028 http://dx.doi.org/10.3390/genes11030339 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Doin de Moura, Ginaini Grazielli
Remigi, Philippe
Masson-Boivin, Catherine
Capela, Delphine
Experimental Evolution of Legume Symbionts: What Have We Learnt?
title Experimental Evolution of Legume Symbionts: What Have We Learnt?
title_full Experimental Evolution of Legume Symbionts: What Have We Learnt?
title_fullStr Experimental Evolution of Legume Symbionts: What Have We Learnt?
title_full_unstemmed Experimental Evolution of Legume Symbionts: What Have We Learnt?
title_short Experimental Evolution of Legume Symbionts: What Have We Learnt?
title_sort experimental evolution of legume symbionts: what have we learnt?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141107/
https://www.ncbi.nlm.nih.gov/pubmed/32210028
http://dx.doi.org/10.3390/genes11030339
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