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Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation

Mutualism is of fundamental importance in ecosystems. Which factors help to keep the relationship mutually beneficial and evolutionarily successful is a central question. We addressed this issue for one of the most significant mutualistic interactions on Earth, which associates plants of the legumin...

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Autores principales: Daubech, Benoit, Remigi, Philippe, Doin de Moura, Ginaini, Marchetti, Marta, Pouzet, Cécile, Auriac, Marie-Christine, Gokhale, Chaitanya S, Masson-Boivin, Catherine, Capela, Delphine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687860/
https://www.ncbi.nlm.nih.gov/pubmed/29022875
http://dx.doi.org/10.7554/eLife.28683
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author Daubech, Benoit
Remigi, Philippe
Doin de Moura, Ginaini
Marchetti, Marta
Pouzet, Cécile
Auriac, Marie-Christine
Gokhale, Chaitanya S
Masson-Boivin, Catherine
Capela, Delphine
author_facet Daubech, Benoit
Remigi, Philippe
Doin de Moura, Ginaini
Marchetti, Marta
Pouzet, Cécile
Auriac, Marie-Christine
Gokhale, Chaitanya S
Masson-Boivin, Catherine
Capela, Delphine
author_sort Daubech, Benoit
collection PubMed
description Mutualism is of fundamental importance in ecosystems. Which factors help to keep the relationship mutually beneficial and evolutionarily successful is a central question. We addressed this issue for one of the most significant mutualistic interactions on Earth, which associates plants of the leguminosae family and hundreds of nitrogen (N(2))-fixing bacterial species. Here we analyze the spatio-temporal dynamics of fixers and non-fixers along the symbiotic process in the Cupriavidus taiwanensis–Mimosa pudica system. N(2)-fixing symbionts progressively outcompete isogenic non-fixers within root nodules, where N(2)-fixation occurs, even when they share the same nodule. Numerical simulations, supported by experimental validation, predict that rare fixers will invade a population dominated by non-fixing bacteria during serial nodulation cycles with a probability that is function of initial inoculum, plant population size and nodulation cycle length. Our findings provide insights into the selective forces and ecological factors that may have driven the spread of the N(2)-fixation mutualistic trait.
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spelling pubmed-56878602017-11-17 Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation Daubech, Benoit Remigi, Philippe Doin de Moura, Ginaini Marchetti, Marta Pouzet, Cécile Auriac, Marie-Christine Gokhale, Chaitanya S Masson-Boivin, Catherine Capela, Delphine eLife Evolutionary Biology Mutualism is of fundamental importance in ecosystems. Which factors help to keep the relationship mutually beneficial and evolutionarily successful is a central question. We addressed this issue for one of the most significant mutualistic interactions on Earth, which associates plants of the leguminosae family and hundreds of nitrogen (N(2))-fixing bacterial species. Here we analyze the spatio-temporal dynamics of fixers and non-fixers along the symbiotic process in the Cupriavidus taiwanensis–Mimosa pudica system. N(2)-fixing symbionts progressively outcompete isogenic non-fixers within root nodules, where N(2)-fixation occurs, even when they share the same nodule. Numerical simulations, supported by experimental validation, predict that rare fixers will invade a population dominated by non-fixing bacteria during serial nodulation cycles with a probability that is function of initial inoculum, plant population size and nodulation cycle length. Our findings provide insights into the selective forces and ecological factors that may have driven the spread of the N(2)-fixation mutualistic trait. eLife Sciences Publications, Ltd 2017-10-12 /pmc/articles/PMC5687860/ /pubmed/29022875 http://dx.doi.org/10.7554/eLife.28683 Text en © 2017, Daubech et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Daubech, Benoit
Remigi, Philippe
Doin de Moura, Ginaini
Marchetti, Marta
Pouzet, Cécile
Auriac, Marie-Christine
Gokhale, Chaitanya S
Masson-Boivin, Catherine
Capela, Delphine
Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation
title Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation
title_full Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation
title_fullStr Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation
title_full_unstemmed Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation
title_short Spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation
title_sort spatio-temporal control of mutualism in legumes helps spread symbiotic nitrogen fixation
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687860/
https://www.ncbi.nlm.nih.gov/pubmed/29022875
http://dx.doi.org/10.7554/eLife.28683
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