Poaceae-specific cell wall-derived oligosaccharides activate plant immunity via OsCERK1 during Magnaporthe oryzae infection in rice

文献类型： 外文期刊

第一作者： Yang, Chao

作者： Yang, Chao;Liu, Rui;Pang, Jinhuan;Liu, Jun;Yang, Chao;Liu, Rui;Liu, Jun;Yang, Chao;Liu, Rui;Ren, Bin;Zhou, Huanbin;Wang, Gang;Wang, Ertao

作者机构：

期刊名称：NATURE COMMUNICATIONS （ 影响因子：12.121； 五年影响因子：13.61 ）

ISSN： 2041-1723

年卷期： 2021 年 12 卷 1 期

页码：

收录情况： SCI

摘要： Many phytopathogens secrete cell wall degradation enzymes (CWDEs) to damage host cells and facilitate colonization. As the major components of the plant cell wall, cellulose and hemicellulose are the targets of CWDEs. Damaged plant cells often release damage-associated molecular patterns (DAMPs) to trigger plant immune responses. Here, we establish that the fungal pathogen Magnaporthe oryzae secretes the endoglucanases MoCel12A and MoCel12B during infection of rice (Oryza sativa). These endoglucanases target hemicellulose of the rice cell wall and release two specific oligosaccharides, namely the trisaccharide 3(1)-beta -D-Cellobiosyl-glucose and the tetrasaccharide 3(1)-beta -D-Cellotriosyl-glucose. 3(1)-beta -D-Cellobiosyl-glucose and 3(1)-beta -D-Cellotriosyl-glucose bind the immune receptor OsCERK1 but not the chitin binding protein OsCEBiP. However, they induce the dimerization of OsCERK1 and OsCEBiP. In addition, these Poaceae cell wall-specific oligosaccharides trigger a burst of reactive oxygen species (ROS) that is largely compromised in oscerk1 and oscebip mutants. We conclude that 3(1)-beta -D-Cellobiosyl-glucose and 3(1)-beta -D-Cellotriosyl-glucose are specific DAMPs released from the hemicellulose of rice cell wall, which are perceived by an OsCERK1 and OsCEBiP immune complex during M. oryzae infection in rice. Pathogen entry to plant cells can release cell wall components. Here the authors show that two endoglucanases secreted by the rice blast fungus Magnaporthe oryzae, produce specific oligosaccharides from rice cell walls that trigger immunity by promoting dimerization of OsCERK1 and OsCEBiP receptors.

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