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Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation

The secretory proteome plays an important role in the pathogenesis of phytopathogenic fungi. However, the relationship between the large-scale secretome of phytopathogenic fungi and their lifestyle is not fully understood. In the present study, the secretomes of 150 plant pathogenic fungi were predi...

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Autores principales: Jia, Mingxuan, Gong, Xiaodong, Fan, Mengmeng, Liu, Haoran, Zhou, He, Gu, Shouqin, Liu, Yuwei, Dong, Jingao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156984/
https://www.ncbi.nlm.nih.gov/pubmed/37152749
http://dx.doi.org/10.3389/fmicb.2023.1171618
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author Jia, Mingxuan
Gong, Xiaodong
Fan, Mengmeng
Liu, Haoran
Zhou, He
Gu, Shouqin
Liu, Yuwei
Dong, Jingao
author_facet Jia, Mingxuan
Gong, Xiaodong
Fan, Mengmeng
Liu, Haoran
Zhou, He
Gu, Shouqin
Liu, Yuwei
Dong, Jingao
author_sort Jia, Mingxuan
collection PubMed
description The secretory proteome plays an important role in the pathogenesis of phytopathogenic fungi. However, the relationship between the large-scale secretome of phytopathogenic fungi and their lifestyle is not fully understood. In the present study, the secretomes of 150 plant pathogenic fungi were predicted and the characteristics associated with different lifestyles were investigated. In total, 94,974 secreted proteins (SPs) were predicted from these fungi. The number of the SPs ranged from 64 to 1,662. Among these fungi, hemibiotrophic fungi had the highest number (average of 970) and proportion (7.1%) of SPs. Functional annotation showed that hemibiotrophic and necrotroph fungi, differ from biotrophic and symbiotic fungi, contained much more carbohydrate enzymes, especially polysaccharide lyases and carbohydrate esterases. Furthermore, the core and lifestyle-specific SPs orthogroups were identified. Twenty-seven core orthogroups contained 16% of the total SPs and their motif function annotation was represented by serine carboxypeptidase, carboxylesterase and asparaginase. In contrast, 97 lifestyle-specific orthogroups contained only 1% of the total SPs, with diverse functions such as PAN_AP in hemibiotroph-specific and flavin monooxygenases in necrotroph-specific. Moreover, obligate biotrophic fungi had the largest number of effectors (average of 150), followed by hemibiotrophic fungi (average of 120). Among these effectors, 4,155 had known functional annotation and pectin lyase had the highest proportion in the functionally annotated effectors. In addition, 32 sets of RNA-Seq data on pathogen-host interactions were collected and the expression levels of SPs were higher than that of non-SPs, and the expression level of effector genes was higher in biotrophic and hemibiotrophic fungi than in necrotrophic fungi, while secretase genes were highly expressed in necrotrophic fungi. Finally, the secretory activity of five predicted SPs from Setosphearia turcica was experimentally verified. In conclusion, our results provide a foundation for the study of pathogen-host interaction and help us to understand the fungal lifestyle adaptation.
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spelling pubmed-101569842023-05-05 Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation Jia, Mingxuan Gong, Xiaodong Fan, Mengmeng Liu, Haoran Zhou, He Gu, Shouqin Liu, Yuwei Dong, Jingao Front Microbiol Microbiology The secretory proteome plays an important role in the pathogenesis of phytopathogenic fungi. However, the relationship between the large-scale secretome of phytopathogenic fungi and their lifestyle is not fully understood. In the present study, the secretomes of 150 plant pathogenic fungi were predicted and the characteristics associated with different lifestyles were investigated. In total, 94,974 secreted proteins (SPs) were predicted from these fungi. The number of the SPs ranged from 64 to 1,662. Among these fungi, hemibiotrophic fungi had the highest number (average of 970) and proportion (7.1%) of SPs. Functional annotation showed that hemibiotrophic and necrotroph fungi, differ from biotrophic and symbiotic fungi, contained much more carbohydrate enzymes, especially polysaccharide lyases and carbohydrate esterases. Furthermore, the core and lifestyle-specific SPs orthogroups were identified. Twenty-seven core orthogroups contained 16% of the total SPs and their motif function annotation was represented by serine carboxypeptidase, carboxylesterase and asparaginase. In contrast, 97 lifestyle-specific orthogroups contained only 1% of the total SPs, with diverse functions such as PAN_AP in hemibiotroph-specific and flavin monooxygenases in necrotroph-specific. Moreover, obligate biotrophic fungi had the largest number of effectors (average of 150), followed by hemibiotrophic fungi (average of 120). Among these effectors, 4,155 had known functional annotation and pectin lyase had the highest proportion in the functionally annotated effectors. In addition, 32 sets of RNA-Seq data on pathogen-host interactions were collected and the expression levels of SPs were higher than that of non-SPs, and the expression level of effector genes was higher in biotrophic and hemibiotrophic fungi than in necrotrophic fungi, while secretase genes were highly expressed in necrotrophic fungi. Finally, the secretory activity of five predicted SPs from Setosphearia turcica was experimentally verified. In conclusion, our results provide a foundation for the study of pathogen-host interaction and help us to understand the fungal lifestyle adaptation. Frontiers Media S.A. 2023-04-20 /pmc/articles/PMC10156984/ /pubmed/37152749 http://dx.doi.org/10.3389/fmicb.2023.1171618 Text en Copyright © 2023 Jia, Gong, Fan, Liu, Zhou, Gu, Liu and Dong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jia, Mingxuan
Gong, Xiaodong
Fan, Mengmeng
Liu, Haoran
Zhou, He
Gu, Shouqin
Liu, Yuwei
Dong, Jingao
Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation
title Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation
title_full Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation
title_fullStr Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation
title_full_unstemmed Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation
title_short Identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation
title_sort identification and analysis of the secretome of plant pathogenic fungi reveals lifestyle adaptation
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156984/
https://www.ncbi.nlm.nih.gov/pubmed/37152749
http://dx.doi.org/10.3389/fmicb.2023.1171618
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