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Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease

The role of rhizosphere microbiota in the resistance of tomato plant against soil-borne Fusarium wilt disease (FWD) remains unclear. Here, we showed that the FWD incidence was significantly negatively correlated with the diversity of both rhizosphere bacterial and fungal communities. Using the micro...

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Autores principales: Zhou, Xin, Wang, Jinting, Liu, Fang, Liang, Junmin, Zhao, Peng, Tsui, Clement K. M., Cai, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780251/
https://www.ncbi.nlm.nih.gov/pubmed/36550095
http://dx.doi.org/10.1038/s41467-022-35452-6
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author Zhou, Xin
Wang, Jinting
Liu, Fang
Liang, Junmin
Zhao, Peng
Tsui, Clement K. M.
Cai, Lei
author_facet Zhou, Xin
Wang, Jinting
Liu, Fang
Liang, Junmin
Zhao, Peng
Tsui, Clement K. M.
Cai, Lei
author_sort Zhou, Xin
collection PubMed
description The role of rhizosphere microbiota in the resistance of tomato plant against soil-borne Fusarium wilt disease (FWD) remains unclear. Here, we showed that the FWD incidence was significantly negatively correlated with the diversity of both rhizosphere bacterial and fungal communities. Using the microbiological culturomic approach, we selected 205 unique strains to construct different synthetic communities (SynComs), which were inoculated into germ-free tomato seedlings, and their roles in suppressing FWD were monitored using omics approach. Cross-kingdom (fungi and bacteria) SynComs were most effective in suppressing FWD than those of Fungal or Bacterial SynComs alone. This effect was underpinned by a combination of molecular mechanisms related to plant immunity and microbial interactions contributed by the bacterial and fungal communities. This study provides new insight into the dynamics of microbiota in pathogen suppression and host immunity interactions. Also, the formulation and manipulation of SynComs for functional complementation constitute a beneficial strategy in controlling soil-borne disease.
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spelling pubmed-97802512022-12-24 Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease Zhou, Xin Wang, Jinting Liu, Fang Liang, Junmin Zhao, Peng Tsui, Clement K. M. Cai, Lei Nat Commun Article The role of rhizosphere microbiota in the resistance of tomato plant against soil-borne Fusarium wilt disease (FWD) remains unclear. Here, we showed that the FWD incidence was significantly negatively correlated with the diversity of both rhizosphere bacterial and fungal communities. Using the microbiological culturomic approach, we selected 205 unique strains to construct different synthetic communities (SynComs), which were inoculated into germ-free tomato seedlings, and their roles in suppressing FWD were monitored using omics approach. Cross-kingdom (fungi and bacteria) SynComs were most effective in suppressing FWD than those of Fungal or Bacterial SynComs alone. This effect was underpinned by a combination of molecular mechanisms related to plant immunity and microbial interactions contributed by the bacterial and fungal communities. This study provides new insight into the dynamics of microbiota in pathogen suppression and host immunity interactions. Also, the formulation and manipulation of SynComs for functional complementation constitute a beneficial strategy in controlling soil-borne disease. Nature Publishing Group UK 2022-12-22 /pmc/articles/PMC9780251/ /pubmed/36550095 http://dx.doi.org/10.1038/s41467-022-35452-6 Text en © The Author(s) 2022, corrected publication 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhou, Xin
Wang, Jinting
Liu, Fang
Liang, Junmin
Zhao, Peng
Tsui, Clement K. M.
Cai, Lei
Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease
title Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease
title_full Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease
title_fullStr Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease
title_full_unstemmed Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease
title_short Cross-kingdom synthetic microbiota supports tomato suppression of Fusarium wilt disease
title_sort cross-kingdom synthetic microbiota supports tomato suppression of fusarium wilt disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780251/
https://www.ncbi.nlm.nih.gov/pubmed/36550095
http://dx.doi.org/10.1038/s41467-022-35452-6
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