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Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice

Increasing evidence suggests that the plant rhizosphere may recruit beneficial microbes to suppress soil-borne pathogens, but microbiome assembly due to foliar pathogen infection and ecological mechanisms that govern microbiome assembly and functions in the diseased host are not fully understood. To...

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Autores principales: Dastogeer, Khondoker M. G., Yasuda, Michiko, Okazaki, Shin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379101/
https://www.ncbi.nlm.nih.gov/pubmed/35983324
http://dx.doi.org/10.3389/fmicb.2022.949152
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author Dastogeer, Khondoker M. G.
Yasuda, Michiko
Okazaki, Shin
author_facet Dastogeer, Khondoker M. G.
Yasuda, Michiko
Okazaki, Shin
author_sort Dastogeer, Khondoker M. G.
collection PubMed
description Increasing evidence suggests that the plant rhizosphere may recruit beneficial microbes to suppress soil-borne pathogens, but microbiome assembly due to foliar pathogen infection and ecological mechanisms that govern microbiome assembly and functions in the diseased host are not fully understood. To provide a comprehensive view of the rice-associated microbiome, we compared bacterial and fungal communities of healthy rice and those infected with Magnaporthe oryzae, the causal agent of blast disease. We found that the soil had a greater diversity of bacterial and fungal communities than plant endospheric communities. There was no significant dysbiosis of bacterial and fungal microbiome diversity due to disease, but it caused a substantial alteration of bacterial community structure in the root and rhizosphere compartments. The pathobiome analysis showed that the microbiome community structure of leaf and grain tissues was changed markedly at the pathogen infection site, although the alpha diversity did not change. Correspondingly, the relative abundances of some bacteria and fungi were clearly altered in symptomatic tissues. We noted an increase in Rhizobium bacteria and a decline of Tylospora, Clohesyomyces, and Penicillium fungi in the symptomatic leaf and grain tissues from both locations. According to the inferred microbial network, several direct interactions between M. oryzae and other microbes were identified. The majority of edges in the interaction network were positive in diseased samples; contrastingly, the number of edges was much lower in the healthy samples. With source tracking analysis, we observed a sharp contrast in the source of root endosphere bacteria due to Magnaporthe infection. Whereas the majority (71%) of healthy root bacteria could be tracked from the soil, only a very small portion (17%) could be tracked from the soil for diseased samples. These results advanced our understanding and provided potential ideas and a theoretical basis for studying pathobiome and exploiting the microbiome for sustainable agriculture.
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spelling pubmed-93791012022-08-17 Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice Dastogeer, Khondoker M. G. Yasuda, Michiko Okazaki, Shin Front Microbiol Microbiology Increasing evidence suggests that the plant rhizosphere may recruit beneficial microbes to suppress soil-borne pathogens, but microbiome assembly due to foliar pathogen infection and ecological mechanisms that govern microbiome assembly and functions in the diseased host are not fully understood. To provide a comprehensive view of the rice-associated microbiome, we compared bacterial and fungal communities of healthy rice and those infected with Magnaporthe oryzae, the causal agent of blast disease. We found that the soil had a greater diversity of bacterial and fungal communities than plant endospheric communities. There was no significant dysbiosis of bacterial and fungal microbiome diversity due to disease, but it caused a substantial alteration of bacterial community structure in the root and rhizosphere compartments. The pathobiome analysis showed that the microbiome community structure of leaf and grain tissues was changed markedly at the pathogen infection site, although the alpha diversity did not change. Correspondingly, the relative abundances of some bacteria and fungi were clearly altered in symptomatic tissues. We noted an increase in Rhizobium bacteria and a decline of Tylospora, Clohesyomyces, and Penicillium fungi in the symptomatic leaf and grain tissues from both locations. According to the inferred microbial network, several direct interactions between M. oryzae and other microbes were identified. The majority of edges in the interaction network were positive in diseased samples; contrastingly, the number of edges was much lower in the healthy samples. With source tracking analysis, we observed a sharp contrast in the source of root endosphere bacteria due to Magnaporthe infection. Whereas the majority (71%) of healthy root bacteria could be tracked from the soil, only a very small portion (17%) could be tracked from the soil for diseased samples. These results advanced our understanding and provided potential ideas and a theoretical basis for studying pathobiome and exploiting the microbiome for sustainable agriculture. Frontiers Media S.A. 2022-08-02 /pmc/articles/PMC9379101/ /pubmed/35983324 http://dx.doi.org/10.3389/fmicb.2022.949152 Text en Copyright © 2022 Dastogeer, Yasuda and Okazaki. 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 Microbiology
Dastogeer, Khondoker M. G.
Yasuda, Michiko
Okazaki, Shin
Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice
title Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice
title_full Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice
title_fullStr Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice
title_full_unstemmed Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice
title_short Microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice
title_sort microbiome and pathobiome analyses reveal changes in community structure by foliar pathogen infection in rice
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9379101/
https://www.ncbi.nlm.nih.gov/pubmed/35983324
http://dx.doi.org/10.3389/fmicb.2022.949152
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