Cargando…

VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis

Apple valsa canker caused by the Ascomycete fungus Valsa mali is one of the most serious diseases of apple, resulting in huge economic losses in the apple-growing area of China. Previous study found that the pathogen could acidify the infected tissues to make lower ambient pH (from 6.0 to 3.5) for t...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Liangsheng, Liu, Hailong, Zhu, Shan, Meng, Yangguang, Wang, Yinghao, Li, Jianyu, Zhang, Feiran, Huang, Lili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441875/
https://www.ncbi.nlm.nih.gov/pubmed/37676527
http://dx.doi.org/10.1007/s44154-023-00097-y
_version_ 1785093467128463360
author Xu, Liangsheng
Liu, Hailong
Zhu, Shan
Meng, Yangguang
Wang, Yinghao
Li, Jianyu
Zhang, Feiran
Huang, Lili
author_facet Xu, Liangsheng
Liu, Hailong
Zhu, Shan
Meng, Yangguang
Wang, Yinghao
Li, Jianyu
Zhang, Feiran
Huang, Lili
author_sort Xu, Liangsheng
collection PubMed
description Apple valsa canker caused by the Ascomycete fungus Valsa mali is one of the most serious diseases of apple, resulting in huge economic losses in the apple-growing area of China. Previous study found that the pathogen could acidify the infected tissues to make lower ambient pH (from 6.0 to 3.5) for their successfully colonization. The pH signaling transcription factor VmPacC is required for acidification of its environment and for full virulence in V. mali. It is known that the functional cooperation of proteins secreted by V. mali plays pivotal role in its successful colonization of host plants. In this study, we used tandem mass tag (TMT) labeling coupled with LC-MS/MS-based quantitative proteomics to analyze the VmPacC-mediated pH regulation in V. mali, focusing on differentially expressed proteins (DEPs). We identified 222 DEPs specific to VmPacC deletion, and 921 DEPs specific to different pH conditions (pH 6.0 and 3.4). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses indicated that these DEPs were mainly involved in pathways associated with carbon metabolism, biosynthesis of antibiotics, citrate cycle (TCA cycle), glycolysis/gluconeogenesis, glutathione metabolism, ribosomes, and pentose phosphate pathways. Additionally, we identified 119 DEPs that were shared among the VmPacC deletion mutant and different pH conditions, which were mainly related to energy metabolism pathways, providing the energy required for the hyphal growth and responses to environmental stresses. A protein-protein interaction (PPI) network analysis indicated that most of the shared proteins were mapped to an interaction network with a medium confidence score of 0.4. Notably, one uncharacterized protein (KUI69106.1), and two known proteins (heat shock protein 60 (KUI73579.1), aspartate aminotransferase (KUI73864.1)) located in the core of the network were highly connected (with ≥ 38 directed edges) with the other shared DEPs. Our results suggest that VmPacC participates in the pathogen’s regulation to ambient pH through the regulation of energy metabolism pathways such as the glycolysis/gluconeogenesis pathway and TCA cycle. Finally, we proposed a sophisticated molecular regulatory network to explain pH decrease in V. mali. Our study, by providing insights into V. mali regulating pH, helps to elucidate the mechanisms of host acidification during pathogen infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s44154-023-00097-y.
format Online
Article
Text
id pubmed-10441875
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Springer Nature Singapore
record_format MEDLINE/PubMed
spelling pubmed-104418752023-08-28 VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis Xu, Liangsheng Liu, Hailong Zhu, Shan Meng, Yangguang Wang, Yinghao Li, Jianyu Zhang, Feiran Huang, Lili Stress Biol Research Apple valsa canker caused by the Ascomycete fungus Valsa mali is one of the most serious diseases of apple, resulting in huge economic losses in the apple-growing area of China. Previous study found that the pathogen could acidify the infected tissues to make lower ambient pH (from 6.0 to 3.5) for their successfully colonization. The pH signaling transcription factor VmPacC is required for acidification of its environment and for full virulence in V. mali. It is known that the functional cooperation of proteins secreted by V. mali plays pivotal role in its successful colonization of host plants. In this study, we used tandem mass tag (TMT) labeling coupled with LC-MS/MS-based quantitative proteomics to analyze the VmPacC-mediated pH regulation in V. mali, focusing on differentially expressed proteins (DEPs). We identified 222 DEPs specific to VmPacC deletion, and 921 DEPs specific to different pH conditions (pH 6.0 and 3.4). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses indicated that these DEPs were mainly involved in pathways associated with carbon metabolism, biosynthesis of antibiotics, citrate cycle (TCA cycle), glycolysis/gluconeogenesis, glutathione metabolism, ribosomes, and pentose phosphate pathways. Additionally, we identified 119 DEPs that were shared among the VmPacC deletion mutant and different pH conditions, which were mainly related to energy metabolism pathways, providing the energy required for the hyphal growth and responses to environmental stresses. A protein-protein interaction (PPI) network analysis indicated that most of the shared proteins were mapped to an interaction network with a medium confidence score of 0.4. Notably, one uncharacterized protein (KUI69106.1), and two known proteins (heat shock protein 60 (KUI73579.1), aspartate aminotransferase (KUI73864.1)) located in the core of the network were highly connected (with ≥ 38 directed edges) with the other shared DEPs. Our results suggest that VmPacC participates in the pathogen’s regulation to ambient pH through the regulation of energy metabolism pathways such as the glycolysis/gluconeogenesis pathway and TCA cycle. Finally, we proposed a sophisticated molecular regulatory network to explain pH decrease in V. mali. Our study, by providing insights into V. mali regulating pH, helps to elucidate the mechanisms of host acidification during pathogen infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s44154-023-00097-y. Springer Nature Singapore 2023-06-21 /pmc/articles/PMC10441875/ /pubmed/37676527 http://dx.doi.org/10.1007/s44154-023-00097-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Xu, Liangsheng
Liu, Hailong
Zhu, Shan
Meng, Yangguang
Wang, Yinghao
Li, Jianyu
Zhang, Feiran
Huang, Lili
VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis
title VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis
title_full VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis
title_fullStr VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis
title_full_unstemmed VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis
title_short VmPacC-mediated pH regulation of Valsa mali confers to host acidification identified by comparative proteomics analysis
title_sort vmpacc-mediated ph regulation of valsa mali confers to host acidification identified by comparative proteomics analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441875/
https://www.ncbi.nlm.nih.gov/pubmed/37676527
http://dx.doi.org/10.1007/s44154-023-00097-y
work_keys_str_mv AT xuliangsheng vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis
AT liuhailong vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis
AT zhushan vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis
AT mengyangguang vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis
AT wangyinghao vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis
AT lijianyu vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis
AT zhangfeiran vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis
AT huanglili vmpaccmediatedphregulationofvalsamaliconferstohostacidificationidentifiedbycomparativeproteomicsanalysis