Author:
Li Jia-xin,Cao Xun-jie,Huang Yuan-yi,Li Ya-ping,Yu Zi-yuan,Lin Min,Li Qiu-ying,Chen Ji-chun,Guo Xu-guang
Abstract
Abstract
Introduction
Staphylococcus aureus is a gram-positive bacterium that causes serious infection. With the increasing resistance of bacteria to current antibiotics, it is necessary to learn more about the molecular mechanism and cellular pathways involved in the Staphylococcus aureus infection.
Methods
We downloaded the GSE33341 dataset from the GEO database and applied the weighted gene co-expression network analysis (WGCNA), from which we obtained some critical modules. Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) were applied to illustrate the biological functions of genes in these modules. We constructed the protein-protein interaction (PPI) network by Cytoscape and selected five candidate hub genes. Five potential hub genes were validated in GSE30119 by GraphPad Prism 8.0. The diagnostic values of these genes were calculated and present in the ROC curve based on the GSE13670 dataset. Their gene functions were analyzed by Gene Set Enrichment Analysis (GSEA).
Results
A co-expression network was built with 5000 genes divided into 11 modules. The genes in green and turquoise modules demonstrated a high correlation. According to the KEGG and GO analyses, genes in the green module were closely related to ubiquitination and autophagy. Subsequently, we picked out the top five hub genes in the green module. And UBB was determined as the hub gene in the GSE30119 dataset. The expression level of UBB, ASB, and MKRN1 could significantly differentiate between Staphylococcus aureus infection and healthy controls based on the ROC curve. The GSEA analysis indicated that lower expression levels of UBB were associated with the P53 signal pathway.
Conclusions
We identified some hub genes and significant signal enrichment pathways in Staphylococcus aureus infection via bioinformatics analysis, which may facilitate the development of potential clinical therapeutic strategies.
Publisher
Springer Science and Business Media LLC
Subject
Microbiology (medical),Microbiology
Reference46 articles.
1. Redi D, Raffaelli CS, Rossetti B, De Luca A, Montagnani F. Staphylococcus aureus vaccine preclinical and clinical development: current state of the art. New Microbiol. 2018;41(3):208–13.
2. Chang J, Lee RE, Lee W. A pursuit of Staphylococcus aureus continues: a role of persister cells. Arch Pharm Res. 2020;43(6):630–8.
3. Melehani JH, Duncan JA. Inflammasome activation can mediate tissue-specific pathogenesis or protection in Staphylococcus aureus infection. Curr Top Microbiol Immunol. 2016;397:257–82.
4. Narita K, Asano K, Nakane A. IL-17A plays an important role in protection induced by vaccination with fibronectin-binding domain of fibronectin-binding protein a against Staphylococcus aureus infection. Med Microbiol Immunol. 2017;206(3):225–34.
5. Stokes W, Parkins MD, Parfitt E, Ruiz JC, Mugford G, Gregson DB. Incidence and outcomes of Staphylococcus aureus bacteriuria: a population-based study. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America. 2019;69(6):963–9.
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