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Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants

Bacterial fruit blotch (BFB), caused by Acidovorax citrulli, seriously affects watermelon and other cucurbit crops, resulting in significant economic losses. However, the pathogenicity mechanism of A. citrulli is not well understood. Plant pathogenic bacteria often suppress the plant immune response...

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Autores principales: Zhang, Xiaoxiao, Zhao, Mei, Jiang, Jie, Yang, Linlin, Yang, Yuwen, Yang, Shanshan, Walcott, Ron, Qiu, Dewen, Zhao, Tingchang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504669/
https://www.ncbi.nlm.nih.gov/pubmed/32842656
http://dx.doi.org/10.3390/ijms21176050
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author Zhang, Xiaoxiao
Zhao, Mei
Jiang, Jie
Yang, Linlin
Yang, Yuwen
Yang, Shanshan
Walcott, Ron
Qiu, Dewen
Zhao, Tingchang
author_facet Zhang, Xiaoxiao
Zhao, Mei
Jiang, Jie
Yang, Linlin
Yang, Yuwen
Yang, Shanshan
Walcott, Ron
Qiu, Dewen
Zhao, Tingchang
author_sort Zhang, Xiaoxiao
collection PubMed
description Bacterial fruit blotch (BFB), caused by Acidovorax citrulli, seriously affects watermelon and other cucurbit crops, resulting in significant economic losses. However, the pathogenicity mechanism of A. citrulli is not well understood. Plant pathogenic bacteria often suppress the plant immune response by secreting effector proteins. Thus, identifying A. citrulli effector proteins and determining their functions may improve our understanding of the underlying pathogenetic mechanisms. In this study, a novel effector, AopN, which is localized on the cell membrane of Nicotiana benthamiana, was identified. The functional analysis revealed that AopN significantly inhibited the flg22-induced reactive oxygen species burst. AopN induced a programmed cell death (PCD) response. Unlike its homologous protein, the ability of AopN to induce PCD was dependent on two motifs of unknown functions (including DUP4129 and Cpta_toxin), but was not dependent on LXXLL domain. More importantly, the virulence of the aopN mutant of A. citrulli in N. benthamiana significantly decreased, indicating that it was a core effector. Further analysis revealed that AopN interacted with watermelon ClHIPP and ClLTP, which responds to A. citrulli strain Aac5 infection at the transcription level. Collectively, these findings indicate that AopN suppresses plant immunity and activates the effector-triggered immunity pathway.
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spelling pubmed-75046692020-09-26 Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants Zhang, Xiaoxiao Zhao, Mei Jiang, Jie Yang, Linlin Yang, Yuwen Yang, Shanshan Walcott, Ron Qiu, Dewen Zhao, Tingchang Int J Mol Sci Article Bacterial fruit blotch (BFB), caused by Acidovorax citrulli, seriously affects watermelon and other cucurbit crops, resulting in significant economic losses. However, the pathogenicity mechanism of A. citrulli is not well understood. Plant pathogenic bacteria often suppress the plant immune response by secreting effector proteins. Thus, identifying A. citrulli effector proteins and determining their functions may improve our understanding of the underlying pathogenetic mechanisms. In this study, a novel effector, AopN, which is localized on the cell membrane of Nicotiana benthamiana, was identified. The functional analysis revealed that AopN significantly inhibited the flg22-induced reactive oxygen species burst. AopN induced a programmed cell death (PCD) response. Unlike its homologous protein, the ability of AopN to induce PCD was dependent on two motifs of unknown functions (including DUP4129 and Cpta_toxin), but was not dependent on LXXLL domain. More importantly, the virulence of the aopN mutant of A. citrulli in N. benthamiana significantly decreased, indicating that it was a core effector. Further analysis revealed that AopN interacted with watermelon ClHIPP and ClLTP, which responds to A. citrulli strain Aac5 infection at the transcription level. Collectively, these findings indicate that AopN suppresses plant immunity and activates the effector-triggered immunity pathway. MDPI 2020-08-22 /pmc/articles/PMC7504669/ /pubmed/32842656 http://dx.doi.org/10.3390/ijms21176050 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Xiaoxiao
Zhao, Mei
Jiang, Jie
Yang, Linlin
Yang, Yuwen
Yang, Shanshan
Walcott, Ron
Qiu, Dewen
Zhao, Tingchang
Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants
title Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants
title_full Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants
title_fullStr Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants
title_full_unstemmed Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants
title_short Identification and Functional Analysis of AopN, an Acidovorax Citrulli Effector that Induces Programmed Cell Death in Plants
title_sort identification and functional analysis of aopn, an acidovorax citrulli effector that induces programmed cell death in plants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504669/
https://www.ncbi.nlm.nih.gov/pubmed/32842656
http://dx.doi.org/10.3390/ijms21176050
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