细胞壁抑制反应蛋白 CwrA 在金黄色葡萄球菌致病性中的作用。

IF 5.5 1区 农林科学 Q1 IMMUNOLOGY
Virulence Pub Date : 2024-12-01 Epub Date: 2024-10-05 DOI:10.1080/21505594.2024.2411540
Weihua Han, Yanghua Xiao, Li Shen, Xinru Yuan, Jingyi Yu, Haojin Gao, Rongrong Hu, Junhong Shi, Bingjie Wang, Jiao Zhang, Peiyao Zhou, Cailing Wan, Yu Huang, JianBo Lv, Fangyou Yu
{"title":"细胞壁抑制反应蛋白 CwrA 在金黄色葡萄球菌致病性中的作用。","authors":"Weihua Han, Yanghua Xiao, Li Shen, Xinru Yuan, Jingyi Yu, Haojin Gao, Rongrong Hu, Junhong Shi, Bingjie Wang, Jiao Zhang, Peiyao Zhou, Cailing Wan, Yu Huang, JianBo Lv, Fangyou Yu","doi":"10.1080/21505594.2024.2411540","DOIUrl":null,"url":null,"abstract":"<p><p>The ability to form robust biofilms and secrete a diverse array of virulence factors are key pathogenic determinants of <i>Staphylococcus aureus</i>, causing a wide range of infectious diseases. Here, we characterized <i>cwrA</i> as a VraR-regulated gene encoding a cell wall inhibition-responsive protein (CwrA) using electrophoretic mobility shift assays. We constructed <i>cwrA</i> deletion mutants in the genetic background of methicillin-resistant <i>S. aureus</i> (MRSA) and methicillin-sensitive <i>S. aureus</i> (MSSA) strains. Phenotypic analyses indicated that deletion of <i>cwrA</i> led to impaired biofilm formation, which was correlated with polysaccharide intercellular adhesin (PIA). Besides, the results of real-time quantitative PCR (RT-qPCR) and β-galactosidase activity assay revealed that CwrA promoted biofilm formation by influence the <i>ica</i> operon activity in <i>S. aureus</i>. Furthermore, <i>cwrA</i> deletion mutants released less extracellular DNA (eDNA) in the biofilm because of their reduced autolytic activity compared to the wild-type (WT) strains. We also found that <i>cwrA</i> deletion mutant more virulence than the parental strain because of its enhanced hemolytic activity. Mechanistically, this phenotypic alteration is related to activation of the SaeRS two-component system, which positively regulates the transcriptional levels of genes encoding membrane-damaging toxins. Overall, our results suggest that CwrA plays an important role in modulating biofilm formation and hemolytic activity in <i>S. aureus</i>.</p>","PeriodicalId":23747,"journal":{"name":"Virulence","volume":null,"pages":null},"PeriodicalIF":5.5000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11457683/pdf/","citationCount":"0","resultStr":"{\"title\":\"The roles of cell wall inhibition responsive protein CwrA in the pathogenicity of <i>Staphylococcus aureus</i>.\",\"authors\":\"Weihua Han, Yanghua Xiao, Li Shen, Xinru Yuan, Jingyi Yu, Haojin Gao, Rongrong Hu, Junhong Shi, Bingjie Wang, Jiao Zhang, Peiyao Zhou, Cailing Wan, Yu Huang, JianBo Lv, Fangyou Yu\",\"doi\":\"10.1080/21505594.2024.2411540\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The ability to form robust biofilms and secrete a diverse array of virulence factors are key pathogenic determinants of <i>Staphylococcus aureus</i>, causing a wide range of infectious diseases. Here, we characterized <i>cwrA</i> as a VraR-regulated gene encoding a cell wall inhibition-responsive protein (CwrA) using electrophoretic mobility shift assays. We constructed <i>cwrA</i> deletion mutants in the genetic background of methicillin-resistant <i>S. aureus</i> (MRSA) and methicillin-sensitive <i>S. aureus</i> (MSSA) strains. Phenotypic analyses indicated that deletion of <i>cwrA</i> led to impaired biofilm formation, which was correlated with polysaccharide intercellular adhesin (PIA). Besides, the results of real-time quantitative PCR (RT-qPCR) and β-galactosidase activity assay revealed that CwrA promoted biofilm formation by influence the <i>ica</i> operon activity in <i>S. aureus</i>. Furthermore, <i>cwrA</i> deletion mutants released less extracellular DNA (eDNA) in the biofilm because of their reduced autolytic activity compared to the wild-type (WT) strains. We also found that <i>cwrA</i> deletion mutant more virulence than the parental strain because of its enhanced hemolytic activity. Mechanistically, this phenotypic alteration is related to activation of the SaeRS two-component system, which positively regulates the transcriptional levels of genes encoding membrane-damaging toxins. Overall, our results suggest that CwrA plays an important role in modulating biofilm formation and hemolytic activity in <i>S. aureus</i>.</p>\",\"PeriodicalId\":23747,\"journal\":{\"name\":\"Virulence\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11457683/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virulence\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1080/21505594.2024.2411540\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virulence","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/21505594.2024.2411540","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

金黄色葡萄球菌具有形成坚固生物膜和分泌多种毒力因子的能力,这是金黄色葡萄球菌导致多种传染性疾病的关键致病决定因素。在这里,我们利用电泳迁移试验鉴定了编码细胞壁抑制反应蛋白(CwrA)的 VraR 调控基因 cwrA。我们在耐甲氧西林金黄色葡萄球菌(MRSA)和甲氧西林敏感金黄色葡萄球菌(MSSA)菌株的遗传背景下构建了 cwrA 缺失突变体。表型分析表明,cwrA缺失会导致生物膜形成受损,这与多糖细胞间粘附素(PIA)有关。此外,实时定量 PCR(RT-qPCR)和 β-半乳糖苷酶活性检测结果表明,CwrA 通过影响金黄色葡萄球菌中 ica 操作子的活性而促进生物膜的形成。此外,与野生型(WT)菌株相比,cwrA缺失突变体由于自溶活性降低,在生物膜中释放的胞外DNA(eDNA)较少。我们还发现,cwrA 缺失突变体的溶血活性增强,因此比亲本菌株的毒力更强。从机理上讲,这种表型改变与 SaeRS 双组分系统的激活有关,该系统对编码膜破坏毒素的基因的转录水平进行正向调节。总之,我们的研究结果表明,CwrA 在调节金黄色葡萄球菌的生物膜形成和溶血活性方面发挥着重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The roles of cell wall inhibition responsive protein CwrA in the pathogenicity of Staphylococcus aureus.

The ability to form robust biofilms and secrete a diverse array of virulence factors are key pathogenic determinants of Staphylococcus aureus, causing a wide range of infectious diseases. Here, we characterized cwrA as a VraR-regulated gene encoding a cell wall inhibition-responsive protein (CwrA) using electrophoretic mobility shift assays. We constructed cwrA deletion mutants in the genetic background of methicillin-resistant S. aureus (MRSA) and methicillin-sensitive S. aureus (MSSA) strains. Phenotypic analyses indicated that deletion of cwrA led to impaired biofilm formation, which was correlated with polysaccharide intercellular adhesin (PIA). Besides, the results of real-time quantitative PCR (RT-qPCR) and β-galactosidase activity assay revealed that CwrA promoted biofilm formation by influence the ica operon activity in S. aureus. Furthermore, cwrA deletion mutants released less extracellular DNA (eDNA) in the biofilm because of their reduced autolytic activity compared to the wild-type (WT) strains. We also found that cwrA deletion mutant more virulence than the parental strain because of its enhanced hemolytic activity. Mechanistically, this phenotypic alteration is related to activation of the SaeRS two-component system, which positively regulates the transcriptional levels of genes encoding membrane-damaging toxins. Overall, our results suggest that CwrA plays an important role in modulating biofilm formation and hemolytic activity in S. aureus.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Virulence
Virulence IMMUNOLOGY-MICROBIOLOGY
CiteScore
9.20
自引率
1.90%
发文量
123
审稿时长
6-12 weeks
期刊介绍: Virulence is a fully open access peer-reviewed journal. All articles will (if accepted) be available for anyone to read anywhere, at any time immediately on publication. Virulence is the first international peer-reviewed journal of its kind to focus exclusively on microbial pathogenicity, the infection process and host-pathogen interactions. To address the new infectious challenges, emerging infectious agents and antimicrobial resistance, there is a clear need for interdisciplinary research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信