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An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection

In plants, the apoplast is a critical battlefield for plant-microbe interactions. Plants secrete defense-related proteins into the apoplast to ward off the invasion of pathogens. How microbial pathogens overcome plant apoplastic immunity remains largely unknown. In this study, we reported that an at...

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Autores principales: Wang, Haonan, Guo, Baodian, Yang, Bo, Li, Haiyang, Xu, Yuanpeng, Zhu, Jinyi, Wang, Yan, Ye, Wenwu, Duan, Kaixuan, Zheng, Xiaobo, Wang, Yuanchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8659694/
https://www.ncbi.nlm.nih.gov/pubmed/34843607
http://dx.doi.org/10.1371/journal.ppat.1010104
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author Wang, Haonan
Guo, Baodian
Yang, Bo
Li, Haiyang
Xu, Yuanpeng
Zhu, Jinyi
Wang, Yan
Ye, Wenwu
Duan, Kaixuan
Zheng, Xiaobo
Wang, Yuanchao
author_facet Wang, Haonan
Guo, Baodian
Yang, Bo
Li, Haiyang
Xu, Yuanpeng
Zhu, Jinyi
Wang, Yan
Ye, Wenwu
Duan, Kaixuan
Zheng, Xiaobo
Wang, Yuanchao
author_sort Wang, Haonan
collection PubMed
description In plants, the apoplast is a critical battlefield for plant-microbe interactions. Plants secrete defense-related proteins into the apoplast to ward off the invasion of pathogens. How microbial pathogens overcome plant apoplastic immunity remains largely unknown. In this study, we reported that an atypical RxLR effector PsAvh181 secreted by Phytophthora sojae, inhibits the secretion of plant defense-related apoplastic proteins. PsAvh181 localizes to plant plasma membrane and essential for P. sojae infection. By co-immunoprecipitation assay followed by liquid chromatography-tandem mass spectrometry analyses, we identified the soybean GmSNAP-1 as a candidate host target of PsAvh181. GmSNAP-1 encodes a soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein, which associates with GmNSF of the SNARE complex functioning in vesicle trafficking. PsAvh181 binds to GmSNAP-1 in vivo and in vitro. PsAvh181 interferes with the interaction between GmSNAP-1 and GmNSF, and blocks the secretion of apoplastic defense-related proteins, such as pathogenesis-related protein PR-1 and apoplastic proteases. Taken together, these data show that an atypical P. sojae RxLR effector suppresses host apoplastic immunity by manipulating the host SNARE complex to interfere with host vesicle trafficking pathway.
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spelling pubmed-86596942021-12-10 An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection Wang, Haonan Guo, Baodian Yang, Bo Li, Haiyang Xu, Yuanpeng Zhu, Jinyi Wang, Yan Ye, Wenwu Duan, Kaixuan Zheng, Xiaobo Wang, Yuanchao PLoS Pathog Research Article In plants, the apoplast is a critical battlefield for plant-microbe interactions. Plants secrete defense-related proteins into the apoplast to ward off the invasion of pathogens. How microbial pathogens overcome plant apoplastic immunity remains largely unknown. In this study, we reported that an atypical RxLR effector PsAvh181 secreted by Phytophthora sojae, inhibits the secretion of plant defense-related apoplastic proteins. PsAvh181 localizes to plant plasma membrane and essential for P. sojae infection. By co-immunoprecipitation assay followed by liquid chromatography-tandem mass spectrometry analyses, we identified the soybean GmSNAP-1 as a candidate host target of PsAvh181. GmSNAP-1 encodes a soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein, which associates with GmNSF of the SNARE complex functioning in vesicle trafficking. PsAvh181 binds to GmSNAP-1 in vivo and in vitro. PsAvh181 interferes with the interaction between GmSNAP-1 and GmNSF, and blocks the secretion of apoplastic defense-related proteins, such as pathogenesis-related protein PR-1 and apoplastic proteases. Taken together, these data show that an atypical P. sojae RxLR effector suppresses host apoplastic immunity by manipulating the host SNARE complex to interfere with host vesicle trafficking pathway. Public Library of Science 2021-11-29 /pmc/articles/PMC8659694/ /pubmed/34843607 http://dx.doi.org/10.1371/journal.ppat.1010104 Text en © 2021 Wang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Wang, Haonan
Guo, Baodian
Yang, Bo
Li, Haiyang
Xu, Yuanpeng
Zhu, Jinyi
Wang, Yan
Ye, Wenwu
Duan, Kaixuan
Zheng, Xiaobo
Wang, Yuanchao
An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection
title An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection
title_full An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection
title_fullStr An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection
title_full_unstemmed An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection
title_short An atypical Phytophthora sojae RxLR effector manipulates host vesicle trafficking to promote infection
title_sort atypical phytophthora sojae rxlr effector manipulates host vesicle trafficking to promote infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8659694/
https://www.ncbi.nlm.nih.gov/pubmed/34843607
http://dx.doi.org/10.1371/journal.ppat.1010104
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