Jingjing Liu, Xinghua Jin, Jingxin Zhu, Jundong Feng, Jian Zhao, Yixuan Wang, Quan Wang, Xiaofeng Song
{"title":"γ Irradiation Alters the <i>Staphylococcus aureus</i> Proteome and Enhances Pathogenicity.","authors":"Jingjing Liu, Xinghua Jin, Jingxin Zhu, Jundong Feng, Jian Zhao, Yixuan Wang, Quan Wang, Xiaofeng Song","doi":"10.1021/acs.jproteome.4c01018","DOIUrl":null,"url":null,"abstract":"<p><p><i>Staphylococcus aureus</i> (<i>S. aureus</i>) infection has become one of the most common and severe complications among cancer patients. The impact of γ radiation from radiotherapy on <i>S. aureus</i>'s growth and virulence is not yet fully understood. In this study, <i>S. aureus</i> was exposed to γ radiation at a dose of 100 Gy, and its descendants were cultured under normal conditions. Proteome alternations of unirradiated, irradiated, and descendants of irradiated <i>S. aureus</i> were identified by using data-independent acquisition (DIA) proteomic technology. To investigate the consequences of proteome alternations induced by γ irradiation in <i>S. aureus</i>, functional enrichment analysis, pathway enrichment analysis, and protein-protein interaction network analysis were performed. Differentially expressed proteins (DEPs) in the irradiated <i>S. aureus</i> and its descendants were primarily enriched in lipoteichoic acid biosynthesis, <i>S. aureus</i> infection, two-component system, and cationic antimicrobial peptide resistance, suggesting an enhanced infection ability. A strong infection ability is typically associated with increased biofilm formation. Both the proteome study and the biofilm assay indicate that γ irradiation enhances the infection ability of <i>S. aureus</i>, likely resulting in increased pathogenicity.</p>","PeriodicalId":48,"journal":{"name":"Journal of Proteome Research","volume":" ","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Proteome Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acs.jproteome.4c01018","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Staphylococcus aureus (S. aureus) infection has become one of the most common and severe complications among cancer patients. The impact of γ radiation from radiotherapy on S. aureus's growth and virulence is not yet fully understood. In this study, S. aureus was exposed to γ radiation at a dose of 100 Gy, and its descendants were cultured under normal conditions. Proteome alternations of unirradiated, irradiated, and descendants of irradiated S. aureus were identified by using data-independent acquisition (DIA) proteomic technology. To investigate the consequences of proteome alternations induced by γ irradiation in S. aureus, functional enrichment analysis, pathway enrichment analysis, and protein-protein interaction network analysis were performed. Differentially expressed proteins (DEPs) in the irradiated S. aureus and its descendants were primarily enriched in lipoteichoic acid biosynthesis, S. aureus infection, two-component system, and cationic antimicrobial peptide resistance, suggesting an enhanced infection ability. A strong infection ability is typically associated with increased biofilm formation. Both the proteome study and the biofilm assay indicate that γ irradiation enhances the infection ability of S. aureus, likely resulting in increased pathogenicity.
期刊介绍:
Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".