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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8857195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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