Persistent Salmonella infections in humans are associated with mutations in the BarA/SirA regulatory pathway

IF 20.6 1区 医学 Q1 MICROBIOLOGY
Alexandra Grote, Bar Piscon, Abigail L. Manson, Boaz Adani, Helit Cohen, Jonathan Livny, Ashlee M. Earl, Ohad Gal-Mor
{"title":"Persistent Salmonella infections in humans are associated with mutations in the BarA/SirA regulatory pathway","authors":"Alexandra Grote, Bar Piscon, Abigail L. Manson, Boaz Adani, Helit Cohen, Jonathan Livny, Ashlee M. Earl, Ohad Gal-Mor","doi":"10.1016/j.chom.2023.12.001","DOIUrl":null,"url":null,"abstract":"<p>Several bacterial pathogens, including <span><em>Salmonella enterica</em></span>, can cause persistent infections in humans by mechanisms that are poorly understood. By comparing genomes of isolates longitudinally collected from 256 prolonged salmonellosis patients, we identified repeated mutations in global regulators, including the <em>barA/sirA</em> two-component regulatory system, across multiple patients and <em>Salmonella</em><span> serovars. Comparative RNA-seq analysis revealed that distinct mutations in </span><em>barA/sirA</em> led to diminished expression of <em>Salmonella</em><span> pathogenicity islands 1 and 4 genes, which are required for </span><em>Salmonella</em><span> invasion and enteritis. Moreover, </span><em>barA/sirA</em><span> mutants were attenuated in an acute salmonellosis mouse model and induced weaker transcription of host immune responses. In contrast, in a persistent infection mouse model, these mutants exhibited long-term colonization and prolonged shedding. Taken together, these findings suggest that selection of mutations in global virulence regulators facilitates persistent </span><em>Salmonella</em> infection in humans, by attenuating <em>Salmonella</em> virulence and inducing a weaker host inflammatory response.</p>","PeriodicalId":9693,"journal":{"name":"Cell host & microbe","volume":"18 1","pages":""},"PeriodicalIF":20.6000,"publicationDate":"2024-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell host & microbe","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.chom.2023.12.001","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Several bacterial pathogens, including Salmonella enterica, can cause persistent infections in humans by mechanisms that are poorly understood. By comparing genomes of isolates longitudinally collected from 256 prolonged salmonellosis patients, we identified repeated mutations in global regulators, including the barA/sirA two-component regulatory system, across multiple patients and Salmonella serovars. Comparative RNA-seq analysis revealed that distinct mutations in barA/sirA led to diminished expression of Salmonella pathogenicity islands 1 and 4 genes, which are required for Salmonella invasion and enteritis. Moreover, barA/sirA mutants were attenuated in an acute salmonellosis mouse model and induced weaker transcription of host immune responses. In contrast, in a persistent infection mouse model, these mutants exhibited long-term colonization and prolonged shedding. Taken together, these findings suggest that selection of mutations in global virulence regulators facilitates persistent Salmonella infection in humans, by attenuating Salmonella virulence and inducing a weaker host inflammatory response.

Abstract Image

人类持续感染沙门氏菌与 BarA/SirA 调控途径中的突变有关
包括肠炎沙门氏菌在内的几种细菌病原体可通过不甚明了的机制导致人类持续感染。通过比较从 256 名长期沙门氏菌病患者身上纵向收集的分离物基因组,我们发现了多个患者和沙门氏菌血清型的全局调控因子(包括 barA/sirA 双组分调控系统)发生了重复突变。RNA-seq比较分析表明,barA/sirA的不同突变导致沙门氏菌致病性岛1和4基因的表达减少,而这两个基因是沙门氏菌入侵和肠炎所必需的。此外,barA/sirA 突变体在急性沙门氏菌病小鼠模型中的作用减弱,诱导的宿主免疫反应转录也减弱。相反,在持续感染小鼠模型中,这些突变体表现出长期定植和长时间脱落。综上所述,这些研究结果表明,全局毒力调节因子突变的选择通过减弱沙门氏菌的毒力和诱导较弱的宿主炎症反应,有利于人类持续感染沙门氏菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cell host & microbe
Cell host & microbe 生物-微生物学
CiteScore
45.10
自引率
1.70%
发文量
201
审稿时长
4-8 weeks
期刊介绍: Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.
×
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