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Three LysM effectors of Zymoseptoria tritici collectively disarm chitin‐triggered plant immunity
Author(s) -
Tian Hui,
MacKenzie Craig I.,
RodriguezMoreno Luis,
Berg Grardy C. M.,
Chen Hongxin,
Rudd Jason J.,
Mesters Jeroen R.,
Thomma Bart P. H. J.
Publication year - 2021
Publication title -
molecular plant pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.945
H-Index - 103
eISSN - 1364-3703
pISSN - 1464-6722
DOI - 10.1111/mpp.13055
Subject(s) - effector , chitin , biology , chitinase , microbiology and biotechnology , virulence , septoria , immunity , hypha , immune system , gene , genetics , botany , biochemistry , chitosan
Chitin is a major structural component of fungal cell walls and acts as a microbe‐associated molecular pattern (MAMP) that, on recognition by a plant host, triggers the activation of immune responses. To avoid the activation of these responses, the Septoria tritici blotch (STB) pathogen of wheat, Zymoseptoria tritici , secretes LysM effector proteins. Previously, the LysM effectors Mg1LysM and Mg3LysM were shown to protect fungal hyphae against host chitinases. Furthermore, Mg3LysM, but not Mg1LysM, was shown to suppress chitin‐induced reactive oxygen species (ROS) production. Whereas initially a third LysM effector gene was disregarded as a presumed pseudogene, we now provide functional data to show that this gene also encodes a LysM effector, named Mgx1LysM, that is functional during wheat colonization. While Mg3LysM confers a major contribution to Z. tritici virulence, Mgx1LysM and Mg1LysM contribute to Z. tritici virulence with smaller effects. All three LysM effectors display partial functional redundancy. We furthermore demonstrate that Mgx1LysM binds chitin, suppresses the chitin‐induced ROS burst, and is able to protect fungal hyphae against chitinase hydrolysis. Finally, we demonstrate that Mgx1LysM is able to undergo chitin‐induced polymerization. Collectively, our data show that Z. tritici utilizes three LysM effectors to disarm chitin‐triggered wheat immunity.

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