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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2023
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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 |
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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 |
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