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A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease

Plant pathogens deliver effectors to alter host processes. Knowledge of how effectors target and manipulate host proteins is critical to understand crop disease. Here, we show that in planta expression of the RXLR effector Pi04314 enhances leaf colonization by Phytophthora infestans via activity in...

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Autores principales: Boevink, Petra C., Wang, Xiaodan, McLellan, Hazel, He, Qin, Naqvi, Shaista, Armstrong, Miles R., Zhang, Wei, Hein, Ingo, Gilroy, Eleanor M., Tian, Zhendong, Birch, Paul R. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740116/
https://www.ncbi.nlm.nih.gov/pubmed/26822079
http://dx.doi.org/10.1038/ncomms10311
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author Boevink, Petra C.
Wang, Xiaodan
McLellan, Hazel
He, Qin
Naqvi, Shaista
Armstrong, Miles R.
Zhang, Wei
Hein, Ingo
Gilroy, Eleanor M.
Tian, Zhendong
Birch, Paul R. J.
author_facet Boevink, Petra C.
Wang, Xiaodan
McLellan, Hazel
He, Qin
Naqvi, Shaista
Armstrong, Miles R.
Zhang, Wei
Hein, Ingo
Gilroy, Eleanor M.
Tian, Zhendong
Birch, Paul R. J.
author_sort Boevink, Petra C.
collection PubMed
description Plant pathogens deliver effectors to alter host processes. Knowledge of how effectors target and manipulate host proteins is critical to understand crop disease. Here, we show that in planta expression of the RXLR effector Pi04314 enhances leaf colonization by Phytophthora infestans via activity in the host nucleus and attenuates induction of jasmonic and salicylic acid-responsive genes. Pi04314 interacts with three host protein phosphatase 1 catalytic (PP1c) isoforms, causing their re-localization from the nucleolus to the nucleoplasm. Re-localization of PP1c-1 also occurs during infection and is dependent on an R/KVxF motif in the effector. Silencing the PP1c isoforms or overexpression of a phosphatase-dead PP1c-1 mutant attenuates infection, demonstrating that host PP1c activity is required for disease. Moreover, expression of PP1c–1mut abolishes enhanced leaf colonization mediated by in planta Pi04314 expression. We argue that PP1c isoforms are susceptibility factors forming holoenzymes with Pi04314 to promote late blight disease.
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spelling pubmed-47401162016-03-04 A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease Boevink, Petra C. Wang, Xiaodan McLellan, Hazel He, Qin Naqvi, Shaista Armstrong, Miles R. Zhang, Wei Hein, Ingo Gilroy, Eleanor M. Tian, Zhendong Birch, Paul R. J. Nat Commun Article Plant pathogens deliver effectors to alter host processes. Knowledge of how effectors target and manipulate host proteins is critical to understand crop disease. Here, we show that in planta expression of the RXLR effector Pi04314 enhances leaf colonization by Phytophthora infestans via activity in the host nucleus and attenuates induction of jasmonic and salicylic acid-responsive genes. Pi04314 interacts with three host protein phosphatase 1 catalytic (PP1c) isoforms, causing their re-localization from the nucleolus to the nucleoplasm. Re-localization of PP1c-1 also occurs during infection and is dependent on an R/KVxF motif in the effector. Silencing the PP1c isoforms or overexpression of a phosphatase-dead PP1c-1 mutant attenuates infection, demonstrating that host PP1c activity is required for disease. Moreover, expression of PP1c–1mut abolishes enhanced leaf colonization mediated by in planta Pi04314 expression. We argue that PP1c isoforms are susceptibility factors forming holoenzymes with Pi04314 to promote late blight disease. Nature Publishing Group 2016-01-29 /pmc/articles/PMC4740116/ /pubmed/26822079 http://dx.doi.org/10.1038/ncomms10311 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Boevink, Petra C.
Wang, Xiaodan
McLellan, Hazel
He, Qin
Naqvi, Shaista
Armstrong, Miles R.
Zhang, Wei
Hein, Ingo
Gilroy, Eleanor M.
Tian, Zhendong
Birch, Paul R. J.
A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease
title A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease
title_full A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease
title_fullStr A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease
title_full_unstemmed A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease
title_short A Phytophthora infestans RXLR effector targets plant PP1c isoforms that promote late blight disease
title_sort phytophthora infestans rxlr effector targets plant pp1c isoforms that promote late blight disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740116/
https://www.ncbi.nlm.nih.gov/pubmed/26822079
http://dx.doi.org/10.1038/ncomms10311
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