Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1783279042901835776 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5687860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT daubechbenoit spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT remigiphilippe spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT doindemouraginaini spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT marchettimarta spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT pouzetcecile spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT auriacmariechristine spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT gokhalechaitanyas spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT massonboivincatherine spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation AT capeladelphine spatiotemporalcontrolofmutualisminlegumeshelpsspreadsymbioticnitrogenfixation |