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The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel

Potassium (K(+)) is required by plants for growth and development, and also contributes to immunity against pathogens. However, it has not been established whether pathogens modulate host K(+) signaling pathways to enhance virulence and subvert host immunity. Here, we show that the effector protein...

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Autores principales: Shi, Xuetao, Long, Yu, He, Feng, Zhang, Chongyang, Wang, Ruyi, Zhang, Ting, Wu, Wei, Hao, Zeyun, Wang, Yi, Wang, Guo-Liang, Ning, Yuese
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809103/
https://www.ncbi.nlm.nih.gov/pubmed/29385213
http://dx.doi.org/10.1371/journal.ppat.1006878
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author Shi, Xuetao
Long, Yu
He, Feng
Zhang, Chongyang
Wang, Ruyi
Zhang, Ting
Wu, Wei
Hao, Zeyun
Wang, Yi
Wang, Guo-Liang
Ning, Yuese
author_facet Shi, Xuetao
Long, Yu
He, Feng
Zhang, Chongyang
Wang, Ruyi
Zhang, Ting
Wu, Wei
Hao, Zeyun
Wang, Yi
Wang, Guo-Liang
Ning, Yuese
author_sort Shi, Xuetao
collection PubMed
description Potassium (K(+)) is required by plants for growth and development, and also contributes to immunity against pathogens. However, it has not been established whether pathogens modulate host K(+) signaling pathways to enhance virulence and subvert host immunity. Here, we show that the effector protein AvrPiz-t from the rice blast pathogen Magnaporthe oryzae targets a K(+) channel to subvert plant immunity. AvrPiz-t interacts with the rice plasma-membrane-localized K(+) channel protein OsAKT1 and specifically suppresses the OsAKT1-mediated K(+) currents. Genetic and phenotypic analyses show that loss of OsAKT1 leads to decreased K(+) content and reduced resistance against M. oryzae. Strikingly, AvrPiz-t interferes with the association of OsAKT1 with its upstream regulator, the cytoplasmic kinase OsCIPK23, which also plays a positive role in K(+) absorption and resistance to M. oryzae. Furthermore, we show a direct correlation between blast disease resistance and external K(+) status in rice plants. Together, our data present a novel mechanism by which a pathogen suppresses plant host immunity by modulating a host K(+) channel.
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spelling pubmed-58091032018-02-28 The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel Shi, Xuetao Long, Yu He, Feng Zhang, Chongyang Wang, Ruyi Zhang, Ting Wu, Wei Hao, Zeyun Wang, Yi Wang, Guo-Liang Ning, Yuese PLoS Pathog Research Article Potassium (K(+)) is required by plants for growth and development, and also contributes to immunity against pathogens. However, it has not been established whether pathogens modulate host K(+) signaling pathways to enhance virulence and subvert host immunity. Here, we show that the effector protein AvrPiz-t from the rice blast pathogen Magnaporthe oryzae targets a K(+) channel to subvert plant immunity. AvrPiz-t interacts with the rice plasma-membrane-localized K(+) channel protein OsAKT1 and specifically suppresses the OsAKT1-mediated K(+) currents. Genetic and phenotypic analyses show that loss of OsAKT1 leads to decreased K(+) content and reduced resistance against M. oryzae. Strikingly, AvrPiz-t interferes with the association of OsAKT1 with its upstream regulator, the cytoplasmic kinase OsCIPK23, which also plays a positive role in K(+) absorption and resistance to M. oryzae. Furthermore, we show a direct correlation between blast disease resistance and external K(+) status in rice plants. Together, our data present a novel mechanism by which a pathogen suppresses plant host immunity by modulating a host K(+) channel. Public Library of Science 2018-01-31 /pmc/articles/PMC5809103/ /pubmed/29385213 http://dx.doi.org/10.1371/journal.ppat.1006878 Text en © 2018 Shi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shi, Xuetao
Long, Yu
He, Feng
Zhang, Chongyang
Wang, Ruyi
Zhang, Ting
Wu, Wei
Hao, Zeyun
Wang, Yi
Wang, Guo-Liang
Ning, Yuese
The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel
title The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel
title_full The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel
title_fullStr The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel
title_full_unstemmed The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel
title_short The fungal pathogen Magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel
title_sort fungal pathogen magnaporthe oryzae suppresses innate immunity by modulating a host potassium channel
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809103/
https://www.ncbi.nlm.nih.gov/pubmed/29385213
http://dx.doi.org/10.1371/journal.ppat.1006878
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