Comparative Secretome Analysis of Magnaporthe oryzae Identified Proteins Involved in Virulence and Cell Wall Integrity

Plant fungal pathogens secrete numerous proteins into the apoplast at the plant–fungus contact sites to facilitate colonization. However, only a few secretory proteins were functionally characterized in Magnaporthe oryzae, the fungal pathogen causing rice blast disease worldwide. Asparagine-linked g...

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Published inGenomics, proteomics & bioinformatics Vol. 20; no. 4; pp. 728 - 746
Main Authors Liu, Ning, Qi, Linlu, Huang, Manna, Chen, Deng, Yin, Changfa, Zhang, Yiying, Wang, Xingbin, Yuan, Guixin, Wang, Rui-Jin, Yang, Jun, Peng, You-Liang, Lu, Xunli
Format Journal Article
LanguageEnglish
Published China Elsevier B.V 01.08.2022
Graduate School of China Agricultural University,Beijing 100193,China%MOA Key Laboratory of Pest Monitoring and Green Management,College of Plant Protection,China Agricultural University,Beijing 100193,China%MOA Key Laboratory of Pest Monitoring and Green Management,College of Plant Protection,China Agricultural University,Beijing 100193,China
Graduate School of China Agricultural University,Beijing 100193,China%State Key Laboratory of Agrobiotechnology and MOA Key Laboratory of Pest Monitoring and Green Management,China Agricultural University,Beijing 100193,China
State Key Laboratory of Agrobiotechnology and MOA Key Laboratory of Pest Monitoring and Green Management,China Agricultural University,Beijing 100193,China
Elsevier
Oxford University Press
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Summary:Plant fungal pathogens secrete numerous proteins into the apoplast at the plant–fungus contact sites to facilitate colonization. However, only a few secretory proteins were functionally characterized in Magnaporthe oryzae, the fungal pathogen causing rice blast disease worldwide. Asparagine-linked glycosylation 3 (Alg3) is an α-1,3-mannosyltransferase functioning in the N-glycan synthesis of N-glycosylated secretory proteins. Fungal pathogenicity and cell wall integrity are impaired in Δalg3 mutants, but the secreted proteins affected in Δalg3 mutants are largely unknown. In this study, we compared the secretomes of the wild-type strain and the Δalg3 mutant and identified 51 proteins that require Alg3 for proper secretion. These proteins were predicted to be involved in metabolic processes, interspecies interactions, cell wall organization, and response to chemicals. Nine proteins were selected for further validation. We found that these proteins were localized at the apoplastic region surrounding the fungal infection hyphae. Moreover, the N-glycosylation of these proteins was significantly changed in the Δalg3 mutant, leading to the decreased protein secretion and abnormal protein localization. Furthermore, we tested the biological functions of two genes, INV1 (encoding invertase 1, a secreted invertase) and AMCase (encoding acid mammalian chinitase, a secreted chitinase). The fungal virulence was significantly reduced, and the cell wall integrity was altered in the Δinv1 and Δamcase mutant strains. Moreover, the N-glycosylation was essential for the function and secretion of AMCase. Taken together, our study provides new insight into the role of N-glycosylated secretory proteins in fungal virulence and cell wall integrity.
ISSN:1672-0229
2210-3244
DOI:10.1016/j.gpb.2021.02.007