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Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis

Plant diseases caused by fungi and oomycetes pose an increasing threat to food security and ecosystem health worldwide. These filamentous pathogens, while taxonomically distinct, modulate host defense responses by secreting effectors, which are typically identified based on the presence of signal pe...

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Autores principales: Liu, Tingli, Song, Tianqiao, Zhang, Xiong, Yuan, Hongbo, Su, Liming, Li, Wanlin, Xu, Jing, Liu, Shiheng, Chen, Linlin, Chen, Tianzi, Zhang, Meixiang, Gu, Lichuan, Zhang, Baolong, Dou, Daolong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348438/
https://www.ncbi.nlm.nih.gov/pubmed/25156390
http://dx.doi.org/10.1038/ncomms5686
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author Liu, Tingli
Song, Tianqiao
Zhang, Xiong
Yuan, Hongbo
Su, Liming
Li, Wanlin
Xu, Jing
Liu, Shiheng
Chen, Linlin
Chen, Tianzi
Zhang, Meixiang
Gu, Lichuan
Zhang, Baolong
Dou, Daolong
author_facet Liu, Tingli
Song, Tianqiao
Zhang, Xiong
Yuan, Hongbo
Su, Liming
Li, Wanlin
Xu, Jing
Liu, Shiheng
Chen, Linlin
Chen, Tianzi
Zhang, Meixiang
Gu, Lichuan
Zhang, Baolong
Dou, Daolong
author_sort Liu, Tingli
collection PubMed
description Plant diseases caused by fungi and oomycetes pose an increasing threat to food security and ecosystem health worldwide. These filamentous pathogens, while taxonomically distinct, modulate host defense responses by secreting effectors, which are typically identified based on the presence of signal peptides. Here we show that Phytophthora sojae and Verticillium dahliae secrete isochorismatases (PsIsc1 and VdIsc1, respectively) that are required for full pathogenesis. PsIsc1 and VdIsc1 can suppress salicylate-mediated innate immunity in planta and hydrolyse isochorismate in vitro. A conserved triad of catalytic residues is essential for both functions. Thus, the two proteins are isochorismatase effectors that disrupt the plant salicylate metabolism pathway by suppressing its precursor. Furthermore, these proteins lack signal peptides, but exhibit characteristics that lead to unconventional secretion. Therefore, this secretion pathway is a novel mechanism for delivering effectors and might play an important role in host–pathogen interactions.
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spelling pubmed-43484382015-03-13 Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis Liu, Tingli Song, Tianqiao Zhang, Xiong Yuan, Hongbo Su, Liming Li, Wanlin Xu, Jing Liu, Shiheng Chen, Linlin Chen, Tianzi Zhang, Meixiang Gu, Lichuan Zhang, Baolong Dou, Daolong Nat Commun Article Plant diseases caused by fungi and oomycetes pose an increasing threat to food security and ecosystem health worldwide. These filamentous pathogens, while taxonomically distinct, modulate host defense responses by secreting effectors, which are typically identified based on the presence of signal peptides. Here we show that Phytophthora sojae and Verticillium dahliae secrete isochorismatases (PsIsc1 and VdIsc1, respectively) that are required for full pathogenesis. PsIsc1 and VdIsc1 can suppress salicylate-mediated innate immunity in planta and hydrolyse isochorismate in vitro. A conserved triad of catalytic residues is essential for both functions. Thus, the two proteins are isochorismatase effectors that disrupt the plant salicylate metabolism pathway by suppressing its precursor. Furthermore, these proteins lack signal peptides, but exhibit characteristics that lead to unconventional secretion. Therefore, this secretion pathway is a novel mechanism for delivering effectors and might play an important role in host–pathogen interactions. Nature Pub. Group 2014-08-26 /pmc/articles/PMC4348438/ /pubmed/25156390 http://dx.doi.org/10.1038/ncomms5686 Text en Copyright © 2014, 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
Liu, Tingli
Song, Tianqiao
Zhang, Xiong
Yuan, Hongbo
Su, Liming
Li, Wanlin
Xu, Jing
Liu, Shiheng
Chen, Linlin
Chen, Tianzi
Zhang, Meixiang
Gu, Lichuan
Zhang, Baolong
Dou, Daolong
Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
title Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
title_full Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
title_fullStr Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
title_full_unstemmed Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
title_short Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
title_sort unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348438/
https://www.ncbi.nlm.nih.gov/pubmed/25156390
http://dx.doi.org/10.1038/ncomms5686
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