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The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions
Pythium oligandrum is a soil-borne oomycete associated with rhizosphere and root tissues. Its ability to enhance plant growth, stimulate plant immunity and parasitize fungal and oomycete preys has led to the development of agricultural biocontrol products. Meanwhile, the effect of P. oligandrum on m...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625430/ https://www.ncbi.nlm.nih.gov/pubmed/37929182 http://dx.doi.org/10.3389/fpls.2023.1156733 |
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author | Hashemi, Maryam Amiel, Aurélien Zouaoui, Mohamed Adam, Kévin Clemente, Hélène San Aguilar, Marielle Pendaries, Rémi Couzigou, Jean-Malo Marti, Guillaume Gaulin, Elodie Roy, Sébastien Rey, Thomas Dumas, Bernard |
author_facet | Hashemi, Maryam Amiel, Aurélien Zouaoui, Mohamed Adam, Kévin Clemente, Hélène San Aguilar, Marielle Pendaries, Rémi Couzigou, Jean-Malo Marti, Guillaume Gaulin, Elodie Roy, Sébastien Rey, Thomas Dumas, Bernard |
author_sort | Hashemi, Maryam |
collection | PubMed |
description | Pythium oligandrum is a soil-borne oomycete associated with rhizosphere and root tissues. Its ability to enhance plant growth, stimulate plant immunity and parasitize fungal and oomycete preys has led to the development of agricultural biocontrol products. Meanwhile, the effect of P. oligandrum on mutualistic interactions and more generally on root microbial communities has not been investigated. Here, we developed a biological system comprising P. oligandrum interacting with two legume plants, Medicago truncatula and Pisum sativum. P. oligandrum activity was investigated at the transcriptomics level through an RNAseq approach, metabolomics and finally metagenomics to investigate the impact of P. oligandrum on root microbiota. We found that P. oligandrum promotes plant growth in these two species and protects them against infection by the oomycete Aphanomyces euteiches, a devastating legume root pathogen. In addition, P. oligandrum up-regulated more than 1000 genes in M. truncatula roots including genes involved in plant defense and notably in the biosynthesis of antimicrobial compounds and validated the enhanced production of M. truncatula phytoalexins, medicarpin and formononetin. Despite this activation of plant immunity, we found that root colonization by P. oligandrum did not impaired symbiotic interactions, promoting the formation of large and multilobed symbiotic nodules with Ensifer meliloti and did not negatively affect the formation of arbuscular mycorrhizal symbiosis. Finally, metagenomic analyses showed the oomycete modifies the composition of fungal and bacterial communities. Together, our results provide novel insights regarding the involvement of P. oligandrum in the functioning of plant root microbiota. |
format | Online Article Text |
id | pubmed-10625430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106254302023-11-05 The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions Hashemi, Maryam Amiel, Aurélien Zouaoui, Mohamed Adam, Kévin Clemente, Hélène San Aguilar, Marielle Pendaries, Rémi Couzigou, Jean-Malo Marti, Guillaume Gaulin, Elodie Roy, Sébastien Rey, Thomas Dumas, Bernard Front Plant Sci Plant Science Pythium oligandrum is a soil-borne oomycete associated with rhizosphere and root tissues. Its ability to enhance plant growth, stimulate plant immunity and parasitize fungal and oomycete preys has led to the development of agricultural biocontrol products. Meanwhile, the effect of P. oligandrum on mutualistic interactions and more generally on root microbial communities has not been investigated. Here, we developed a biological system comprising P. oligandrum interacting with two legume plants, Medicago truncatula and Pisum sativum. P. oligandrum activity was investigated at the transcriptomics level through an RNAseq approach, metabolomics and finally metagenomics to investigate the impact of P. oligandrum on root microbiota. We found that P. oligandrum promotes plant growth in these two species and protects them against infection by the oomycete Aphanomyces euteiches, a devastating legume root pathogen. In addition, P. oligandrum up-regulated more than 1000 genes in M. truncatula roots including genes involved in plant defense and notably in the biosynthesis of antimicrobial compounds and validated the enhanced production of M. truncatula phytoalexins, medicarpin and formononetin. Despite this activation of plant immunity, we found that root colonization by P. oligandrum did not impaired symbiotic interactions, promoting the formation of large and multilobed symbiotic nodules with Ensifer meliloti and did not negatively affect the formation of arbuscular mycorrhizal symbiosis. Finally, metagenomic analyses showed the oomycete modifies the composition of fungal and bacterial communities. Together, our results provide novel insights regarding the involvement of P. oligandrum in the functioning of plant root microbiota. Frontiers Media S.A. 2023-10-20 /pmc/articles/PMC10625430/ /pubmed/37929182 http://dx.doi.org/10.3389/fpls.2023.1156733 Text en Copyright © 2023 Hashemi, Amiel, Zouaoui, Adam, Clemente, Aguilar, Pendaries, Couzigou, Marti, Gaulin, Roy, Rey and Dumas https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Hashemi, Maryam Amiel, Aurélien Zouaoui, Mohamed Adam, Kévin Clemente, Hélène San Aguilar, Marielle Pendaries, Rémi Couzigou, Jean-Malo Marti, Guillaume Gaulin, Elodie Roy, Sébastien Rey, Thomas Dumas, Bernard The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions |
title | The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions |
title_full | The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions |
title_fullStr | The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions |
title_full_unstemmed | The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions |
title_short | The mycoparasite Pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions |
title_sort | mycoparasite pythium oligandrum induces legume pathogen resistance and shapes rhizosphere microbiota without impacting mutualistic interactions |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625430/ https://www.ncbi.nlm.nih.gov/pubmed/37929182 http://dx.doi.org/10.3389/fpls.2023.1156733 |
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