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Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition

The rhizosphere microbiome forms a first line of defense against soilborne pathogens. To date, most microbiome enhancement strategies have relied on bioaugmentation with antagonistic microorganisms that directly inhibit pathogens. Previous studies have shown that some root-associated bacteria are ab...

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Autores principales: Li, Mei, Pommier, Thomas, Yin, Yue, Wang, Jianing, Gu, Shaohua, Jousset, Alexandre, Keuskamp, Joost, Wang, Honggui, Wei, Zhong, Xu, Yangchun, Shen, Qirong, Kowalchuk, George A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857195/
https://www.ncbi.nlm.nih.gov/pubmed/34671104
http://dx.doi.org/10.1038/s41396-021-01126-2
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author Li, Mei
Pommier, Thomas
Yin, Yue
Wang, Jianing
Gu, Shaohua
Jousset, Alexandre
Keuskamp, Joost
Wang, Honggui
Wei, Zhong
Xu, Yangchun
Shen, Qirong
Kowalchuk, George A.
author_facet Li, Mei
Pommier, Thomas
Yin, Yue
Wang, Jianing
Gu, Shaohua
Jousset, Alexandre
Keuskamp, Joost
Wang, Honggui
Wei, Zhong
Xu, Yangchun
Shen, Qirong
Kowalchuk, George A.
author_sort Li, Mei
collection PubMed
description The rhizosphere microbiome forms a first line of defense against soilborne pathogens. To date, most microbiome enhancement strategies have relied on bioaugmentation with antagonistic microorganisms that directly inhibit pathogens. Previous studies have shown that some root-associated bacteria are able to facilitate pathogen growth. We therefore hypothesized that inhibiting such pathogen helpers may help reduce pathogen densities. We examined tripartite interactions between a model pathogen, Ralstonia solanacearum, two model helper strains and a collection of 46 bacterial isolates recovered from the tomato rhizosphere. This system allowed us to examine the importance of direct (effects of rhizobacteria on pathogen growth) and indirect (effects of rhizobacteria on helper growth) pathways affecting pathogen growth. We found that the interaction between rhizosphere isolates and the helper strains was the major determinant of pathogen suppression both in vitro and in vivo. We therefore propose that controlling microbiome composition to prevent the growth of pathogen helpers may become part of sustainable strategies for pathogen control.
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spelling pubmed-88571952022-03-03 Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition Li, Mei Pommier, Thomas Yin, Yue Wang, Jianing Gu, Shaohua Jousset, Alexandre Keuskamp, Joost Wang, Honggui Wei, Zhong Xu, Yangchun Shen, Qirong Kowalchuk, George A. ISME J Article The rhizosphere microbiome forms a first line of defense against soilborne pathogens. To date, most microbiome enhancement strategies have relied on bioaugmentation with antagonistic microorganisms that directly inhibit pathogens. Previous studies have shown that some root-associated bacteria are able to facilitate pathogen growth. We therefore hypothesized that inhibiting such pathogen helpers may help reduce pathogen densities. We examined tripartite interactions between a model pathogen, Ralstonia solanacearum, two model helper strains and a collection of 46 bacterial isolates recovered from the tomato rhizosphere. This system allowed us to examine the importance of direct (effects of rhizobacteria on pathogen growth) and indirect (effects of rhizobacteria on helper growth) pathways affecting pathogen growth. We found that the interaction between rhizosphere isolates and the helper strains was the major determinant of pathogen suppression both in vitro and in vivo. We therefore propose that controlling microbiome composition to prevent the growth of pathogen helpers may become part of sustainable strategies for pathogen control. Nature Publishing Group UK 2021-10-20 2022-03 /pmc/articles/PMC8857195/ /pubmed/34671104 http://dx.doi.org/10.1038/s41396-021-01126-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Mei
Pommier, Thomas
Yin, Yue
Wang, Jianing
Gu, Shaohua
Jousset, Alexandre
Keuskamp, Joost
Wang, Honggui
Wei, Zhong
Xu, Yangchun
Shen, Qirong
Kowalchuk, George A.
Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition
title Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition
title_full Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition
title_fullStr Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition
title_full_unstemmed Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition
title_short Indirect reduction of Ralstonia solanacearum via pathogen helper inhibition
title_sort indirect reduction of ralstonia solanacearum via pathogen helper inhibition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857195/
https://www.ncbi.nlm.nih.gov/pubmed/34671104
http://dx.doi.org/10.1038/s41396-021-01126-2
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