Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783299534251622400 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5809103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT shixuetao thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT longyu thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT hefeng thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT zhangchongyang thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wangruyi thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT zhangting thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wuwei thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT haozeyun thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wangyi thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wangguoliang thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT ningyuese thefungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT shixuetao fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT longyu fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT hefeng fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT zhangchongyang fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wangruyi fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT zhangting fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wuwei fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT haozeyun fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wangyi fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT wangguoliang fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel AT ningyuese fungalpathogenmagnaportheoryzaesuppressesinnateimmunitybymodulatingahostpotassiumchannel |