Serveur d'exploration Phytophthora

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Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis.

Identifieur interne : 000F84 ( Main/Corpus ); précédent : 000F83; suivant : 000F85

Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis.

Auteurs : Tingli Liu ; Tianqiao Song ; Xiong Zhang ; Hongbo Yuan ; Liming Su ; Wanlin Li ; Jing Xu ; Shiheng Liu ; Linlin Chen ; Tianzi Chen ; Meixiang Zhang ; Lichuan Gu ; Baolong Zhang ; Daolong Dou

Source :

RBID : pubmed:25156390

English descriptors

Abstract

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.

DOI: 10.1038/ncomms5686
PubMed: 25156390
PubMed Central: PMC4348438

Links to Exploration step

pubmed:25156390

Le document en format XML

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<term>Gossypium (microbiology)</term>
<term>Gossypium (physiology)</term>
<term>Host-Pathogen Interactions (MeSH)</term>
<term>Hydrolases (genetics)</term>
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<term>Phytophthora (pathogenicity)</term>
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<div type="abstract" xml:lang="en">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. </div>
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<AbstractText>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. </AbstractText>
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