Cargando…

Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency

Legume plants can form root organs called nodules where they house intracellular symbiotic rhizobium bacteria. Within nodule cells, rhizobia differentiate into bacteroids, which fix nitrogen for the benefit of the plant. Depending on the combination of host plants and rhizobial strains, the output o...

Descripción completa

Detalles Bibliográficos
Autores principales: Nicoud, Quentin, Lamouche, Florian, Chaumeret, Anaïs, Balliau, Thierry, Le Bars, Romain, Bourge, Mickaël, Pierre, Fabienne, Guérard, Florence, Sallet, Erika, Tuffigo, Solenn, Pierre, Olivier, Dessaux, Yves, Gilard, Françoise, Gakière, Bertrand, Nagy, Istvan, Kereszt, Attila, Zivy, Michel, Mergaert, Peter, Gourion, Benjamin, Alunni, Benoit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8125078/
https://www.ncbi.nlm.nih.gov/pubmed/33975972
http://dx.doi.org/10.1128/mSystems.01237-20
_version_ 1783693395061899264
author Nicoud, Quentin
Lamouche, Florian
Chaumeret, Anaïs
Balliau, Thierry
Le Bars, Romain
Bourge, Mickaël
Pierre, Fabienne
Guérard, Florence
Sallet, Erika
Tuffigo, Solenn
Pierre, Olivier
Dessaux, Yves
Gilard, Françoise
Gakière, Bertrand
Nagy, Istvan
Kereszt, Attila
Zivy, Michel
Mergaert, Peter
Gourion, Benjamin
Alunni, Benoit
author_facet Nicoud, Quentin
Lamouche, Florian
Chaumeret, Anaïs
Balliau, Thierry
Le Bars, Romain
Bourge, Mickaël
Pierre, Fabienne
Guérard, Florence
Sallet, Erika
Tuffigo, Solenn
Pierre, Olivier
Dessaux, Yves
Gilard, Françoise
Gakière, Bertrand
Nagy, Istvan
Kereszt, Attila
Zivy, Michel
Mergaert, Peter
Gourion, Benjamin
Alunni, Benoit
author_sort Nicoud, Quentin
collection PubMed
description Legume plants can form root organs called nodules where they house intracellular symbiotic rhizobium bacteria. Within nodule cells, rhizobia differentiate into bacteroids, which fix nitrogen for the benefit of the plant. Depending on the combination of host plants and rhizobial strains, the output of rhizobium-legume interactions varies from nonfixing associations to symbioses that are highly beneficial for the plant. Bradyrhizobium diazoefficiens USDA110 was isolated as a soybean symbiont, but it can also establish a functional symbiotic interaction with Aeschynomene afraspera. In contrast to soybean, A. afraspera triggers terminal bacteroid differentiation, a process involving bacterial cell elongation, polyploidy, and increased membrane permeability, leading to a loss of bacterial viability while plants increase their symbiotic benefit. A combination of plant metabolomics, bacterial proteomics, and transcriptomics along with cytological analyses were used to study the physiology of USDA110 bacteroids in these two host plants. We show that USDA110 establishes a poorly efficient symbiosis with A. afraspera despite the full activation of the bacterial symbiotic program. We found molecular signatures of high levels of stress in A. afraspera bacteroids, whereas those of terminal bacteroid differentiation were only partially activated. Finally, we show that in A. afraspera, USDA110 bacteroids undergo atypical terminal differentiation hallmarked by the disconnection of the canonical features of this process. This study pinpoints how a rhizobium strain can adapt its physiology to a new host and cope with terminal differentiation when it did not coevolve with such a host. IMPORTANCE Legume-rhizobium symbiosis is a major ecological process in the nitrogen cycle, responsible for the main input of fixed nitrogen into the biosphere. The efficiency of this symbiosis relies on the coevolution of the partners. Some, but not all, legume plants optimize their return on investment in the symbiosis by imposing on their microsymbionts a terminal differentiation program that increases their symbiotic efficiency but imposes a high level of stress and drastically reduces their viability. We combined multi-omics with physiological analyses to show that the symbiotic couple formed by Bradyrhizobium diazoefficiens USDA110 and Aeschynomene afraspera, in which the host and symbiont did not evolve together, is functional but displays a low symbiotic efficiency associated with a disconnection of terminal bacteroid differentiation features.
format Online
Article
Text
id pubmed-8125078
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-81250782021-06-09 Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency Nicoud, Quentin Lamouche, Florian Chaumeret, Anaïs Balliau, Thierry Le Bars, Romain Bourge, Mickaël Pierre, Fabienne Guérard, Florence Sallet, Erika Tuffigo, Solenn Pierre, Olivier Dessaux, Yves Gilard, Françoise Gakière, Bertrand Nagy, Istvan Kereszt, Attila Zivy, Michel Mergaert, Peter Gourion, Benjamin Alunni, Benoit mSystems Research Article Legume plants can form root organs called nodules where they house intracellular symbiotic rhizobium bacteria. Within nodule cells, rhizobia differentiate into bacteroids, which fix nitrogen for the benefit of the plant. Depending on the combination of host plants and rhizobial strains, the output of rhizobium-legume interactions varies from nonfixing associations to symbioses that are highly beneficial for the plant. Bradyrhizobium diazoefficiens USDA110 was isolated as a soybean symbiont, but it can also establish a functional symbiotic interaction with Aeschynomene afraspera. In contrast to soybean, A. afraspera triggers terminal bacteroid differentiation, a process involving bacterial cell elongation, polyploidy, and increased membrane permeability, leading to a loss of bacterial viability while plants increase their symbiotic benefit. A combination of plant metabolomics, bacterial proteomics, and transcriptomics along with cytological analyses were used to study the physiology of USDA110 bacteroids in these two host plants. We show that USDA110 establishes a poorly efficient symbiosis with A. afraspera despite the full activation of the bacterial symbiotic program. We found molecular signatures of high levels of stress in A. afraspera bacteroids, whereas those of terminal bacteroid differentiation were only partially activated. Finally, we show that in A. afraspera, USDA110 bacteroids undergo atypical terminal differentiation hallmarked by the disconnection of the canonical features of this process. This study pinpoints how a rhizobium strain can adapt its physiology to a new host and cope with terminal differentiation when it did not coevolve with such a host. IMPORTANCE Legume-rhizobium symbiosis is a major ecological process in the nitrogen cycle, responsible for the main input of fixed nitrogen into the biosphere. The efficiency of this symbiosis relies on the coevolution of the partners. Some, but not all, legume plants optimize their return on investment in the symbiosis by imposing on their microsymbionts a terminal differentiation program that increases their symbiotic efficiency but imposes a high level of stress and drastically reduces their viability. We combined multi-omics with physiological analyses to show that the symbiotic couple formed by Bradyrhizobium diazoefficiens USDA110 and Aeschynomene afraspera, in which the host and symbiont did not evolve together, is functional but displays a low symbiotic efficiency associated with a disconnection of terminal bacteroid differentiation features. American Society for Microbiology 2021-05-11 /pmc/articles/PMC8125078/ /pubmed/33975972 http://dx.doi.org/10.1128/mSystems.01237-20 Text en Copyright © 2021 Nicoud et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Nicoud, Quentin
Lamouche, Florian
Chaumeret, Anaïs
Balliau, Thierry
Le Bars, Romain
Bourge, Mickaël
Pierre, Fabienne
Guérard, Florence
Sallet, Erika
Tuffigo, Solenn
Pierre, Olivier
Dessaux, Yves
Gilard, Françoise
Gakière, Bertrand
Nagy, Istvan
Kereszt, Attila
Zivy, Michel
Mergaert, Peter
Gourion, Benjamin
Alunni, Benoit
Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency
title Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency
title_full Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency
title_fullStr Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency
title_full_unstemmed Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency
title_short Bradyrhizobium diazoefficiens USDA110 Nodulation of Aeschynomene afraspera Is Associated with Atypical Terminal Bacteroid Differentiation and Suboptimal Symbiotic Efficiency
title_sort bradyrhizobium diazoefficiens usda110 nodulation of aeschynomene afraspera is associated with atypical terminal bacteroid differentiation and suboptimal symbiotic efficiency
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8125078/
https://www.ncbi.nlm.nih.gov/pubmed/33975972
http://dx.doi.org/10.1128/mSystems.01237-20
work_keys_str_mv AT nicoudquentin bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT lamoucheflorian bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT chaumeretanais bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT balliauthierry bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT lebarsromain bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT bourgemickael bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT pierrefabienne bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT guerardflorence bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT salleterika bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT tuffigosolenn bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT pierreolivier bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT dessauxyves bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT gilardfrancoise bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT gakierebertrand bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT nagyistvan bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT keresztattila bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT zivymichel bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT mergaertpeter bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT gourionbenjamin bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency
AT alunnibenoit bradyrhizobiumdiazoefficiensusda110nodulationofaeschynomeneafrasperaisassociatedwithatypicalterminalbacteroiddifferentiationandsuboptimalsymbioticefficiency