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Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles

Extracellular vesicles (EVs) are important for cell-to-cell communication in animals. EVs also play important roles in plant–microbe interactions, but the underlying mechanisms remain elusive. Here, proteomic analyses of EVs from the soybean (Glycine max) root rot pathogen Phytophthora sojae identif...

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Autores principales: Zhu, Jinyi, Qiao, Qian, Sun, Yujing, Xu, Yuanpeng, Shu, Haidong, Zhang, Zhichao, Liu, Fan, Wang, Haonan, Ye, Wenwu, Dong, Suomeng, Wang, Yan, Ma, Zhenchuan, Wang, Yuanchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423219/
https://www.ncbi.nlm.nih.gov/pubmed/37573360
http://dx.doi.org/10.1038/s41467-023-40623-0
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author Zhu, Jinyi
Qiao, Qian
Sun, Yujing
Xu, Yuanpeng
Shu, Haidong
Zhang, Zhichao
Liu, Fan
Wang, Haonan
Ye, Wenwu
Dong, Suomeng
Wang, Yan
Ma, Zhenchuan
Wang, Yuanchao
author_facet Zhu, Jinyi
Qiao, Qian
Sun, Yujing
Xu, Yuanpeng
Shu, Haidong
Zhang, Zhichao
Liu, Fan
Wang, Haonan
Ye, Wenwu
Dong, Suomeng
Wang, Yan
Ma, Zhenchuan
Wang, Yuanchao
author_sort Zhu, Jinyi
collection PubMed
description Extracellular vesicles (EVs) are important for cell-to-cell communication in animals. EVs also play important roles in plant–microbe interactions, but the underlying mechanisms remain elusive. Here, proteomic analyses of EVs from the soybean (Glycine max) root rot pathogen Phytophthora sojae identify the tetraspanin family proteins PsTET1 and PsTET3, which are recognized by Nicotiana benthamiana to trigger plant immune responses. Both proteins are required for the full virulence of P. sojae. The large extracellular loop (EC2) of PsTET3 is the key region recognized by N. benthamiana and soybean cells in a plant receptor-like kinase NbSERK3a/b dependent manner. TET proteins from oomycete and fungal plant pathogens are recognized by N. benthamiana thus inducing immune responses, whereas plant-derived TET proteins are not due to the sequence divergence of sixteen amino acids at the C-terminal of EC2. This feature allows plants to distinguish self and non-self EVs to trigger active defense responses against pathogenic eukaryotes.
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spelling pubmed-104232192023-08-14 Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles Zhu, Jinyi Qiao, Qian Sun, Yujing Xu, Yuanpeng Shu, Haidong Zhang, Zhichao Liu, Fan Wang, Haonan Ye, Wenwu Dong, Suomeng Wang, Yan Ma, Zhenchuan Wang, Yuanchao Nat Commun Article Extracellular vesicles (EVs) are important for cell-to-cell communication in animals. EVs also play important roles in plant–microbe interactions, but the underlying mechanisms remain elusive. Here, proteomic analyses of EVs from the soybean (Glycine max) root rot pathogen Phytophthora sojae identify the tetraspanin family proteins PsTET1 and PsTET3, which are recognized by Nicotiana benthamiana to trigger plant immune responses. Both proteins are required for the full virulence of P. sojae. The large extracellular loop (EC2) of PsTET3 is the key region recognized by N. benthamiana and soybean cells in a plant receptor-like kinase NbSERK3a/b dependent manner. TET proteins from oomycete and fungal plant pathogens are recognized by N. benthamiana thus inducing immune responses, whereas plant-derived TET proteins are not due to the sequence divergence of sixteen amino acids at the C-terminal of EC2. This feature allows plants to distinguish self and non-self EVs to trigger active defense responses against pathogenic eukaryotes. Nature Publishing Group UK 2023-08-12 /pmc/articles/PMC10423219/ /pubmed/37573360 http://dx.doi.org/10.1038/s41467-023-40623-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhu, Jinyi
Qiao, Qian
Sun, Yujing
Xu, Yuanpeng
Shu, Haidong
Zhang, Zhichao
Liu, Fan
Wang, Haonan
Ye, Wenwu
Dong, Suomeng
Wang, Yan
Ma, Zhenchuan
Wang, Yuanchao
Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles
title Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles
title_full Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles
title_fullStr Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles
title_full_unstemmed Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles
title_short Divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles
title_sort divergent sequences of tetraspanins enable plants to specifically recognize microbe-derived extracellular vesicles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423219/
https://www.ncbi.nlm.nih.gov/pubmed/37573360
http://dx.doi.org/10.1038/s41467-023-40623-0
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