Infection-relevant conditions dictate differential versus coordinate expression of Salmonella chaperones and cochaperones.

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-05-14 Epub Date: 2025-03-31 DOI:10.1128/mbio.00227-25
Carissa Chan, Keiichiro Mukai, Eduardo A Groisman
{"title":"Infection-relevant conditions dictate differential versus coordinate expression of <i>Salmonella</i> chaperones and cochaperones.","authors":"Carissa Chan, Keiichiro Mukai, Eduardo A Groisman","doi":"10.1128/mbio.00227-25","DOIUrl":null,"url":null,"abstract":"<p><p>Molecular chaperones are critical for protein homeostasis. In bacteria, chaperone trigger factor (TF) folds proteins co-translationally, and chaperone DnaK requires a J-domain cochaperone and nucleotide exchange factor GrpE to fold proteins largely post-translationally. However, when the pathogen <i>Salmonella enterica</i> serovar Typhimurium faces the infection-relevant condition of cytoplasmic Mg<sup>2+</sup> starvation, DnaK reduces protein synthesis independently. This raises the possibility that bacteria differentially express chaperones and cochaperones. We now report that <i>S</i>. Typhimurium responds to cytoplasmic Mg<sup>2+</sup> starvation by increasing mRNA amounts of <i>dnaK</i> while decreasing those of the TF-encoding gene <i>tig</i> and J-domain cochaperone genes <i>dnaJ</i> and <i>djlA</i>. This differential strategy requires the master regulator of Mg<sup>2+</sup> homeostasis and virulence PhoP, which increases <i>dnaK</i> mRNA amounts by lowering the ATP concentration, thereby hindering proteolysis of the alternative sigma factor RpoH responsible for <i>dnaK</i> transcription. We also establish that DnaK exerts negative feedback on the RpoH protein and RpoH-dependent transcripts independently of J-domain cochaperones. Thus, bacteria express chaperones and cochaperones coordinately or differentially depending on the specific stress perturbing protein homeostasis.IMPORTANCEMolecular chaperones typically require cochaperones to fold proteins and to prevent protein aggregation, and the corresponding genes are thus coordinately expressed. We have now identified an infection-relevant stress condition in which the genes specifying chaperone DnaK and cochaperone DnaJ are differentially expressed despite belonging to the same operon. This differential strategy requires the master regulator of Mg<sup>2+</sup> homeostasis and virulence in the pathogen <i>Salmonella enterica</i> serovar Typhimurium. Moreover, it likely reflects that <i>Salmonella</i> requires <i>dnaK</i>, but not J-domain cochaperone-encoding genes, for survival against cytoplasmic Mg<sup>2+</sup> starvation and expresses genes only when needed. Thus, the specific condition impacting protein homeostasis determines the coordinate versus differential expression of molecular chaperones and cochaperones.</p>","PeriodicalId":18315,"journal":{"name":"mBio","volume":" ","pages":"e0022725"},"PeriodicalIF":5.1000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12077118/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"mBio","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/mbio.00227-25","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/31 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Molecular chaperones are critical for protein homeostasis. In bacteria, chaperone trigger factor (TF) folds proteins co-translationally, and chaperone DnaK requires a J-domain cochaperone and nucleotide exchange factor GrpE to fold proteins largely post-translationally. However, when the pathogen Salmonella enterica serovar Typhimurium faces the infection-relevant condition of cytoplasmic Mg2+ starvation, DnaK reduces protein synthesis independently. This raises the possibility that bacteria differentially express chaperones and cochaperones. We now report that S. Typhimurium responds to cytoplasmic Mg2+ starvation by increasing mRNA amounts of dnaK while decreasing those of the TF-encoding gene tig and J-domain cochaperone genes dnaJ and djlA. This differential strategy requires the master regulator of Mg2+ homeostasis and virulence PhoP, which increases dnaK mRNA amounts by lowering the ATP concentration, thereby hindering proteolysis of the alternative sigma factor RpoH responsible for dnaK transcription. We also establish that DnaK exerts negative feedback on the RpoH protein and RpoH-dependent transcripts independently of J-domain cochaperones. Thus, bacteria express chaperones and cochaperones coordinately or differentially depending on the specific stress perturbing protein homeostasis.IMPORTANCEMolecular chaperones typically require cochaperones to fold proteins and to prevent protein aggregation, and the corresponding genes are thus coordinately expressed. We have now identified an infection-relevant stress condition in which the genes specifying chaperone DnaK and cochaperone DnaJ are differentially expressed despite belonging to the same operon. This differential strategy requires the master regulator of Mg2+ homeostasis and virulence in the pathogen Salmonella enterica serovar Typhimurium. Moreover, it likely reflects that Salmonella requires dnaK, but not J-domain cochaperone-encoding genes, for survival against cytoplasmic Mg2+ starvation and expresses genes only when needed. Thus, the specific condition impacting protein homeostasis determines the coordinate versus differential expression of molecular chaperones and cochaperones.

感染相关条件决定了沙门氏菌伴侣蛋白和伴侣蛋白的差异与协调表达。
分子伴侣对蛋白质稳态至关重要。在细菌中,伴侣触发因子(TF)在共翻译中折叠蛋白质,而伴侣DnaK需要j结构域的伴侣和核苷酸交换因子GrpE来在翻译后折叠蛋白质。然而,当致病菌肠沙门氏菌血清型鼠伤寒沙门氏菌面临细胞质Mg2+饥饿的感染相关条件时,DnaK可独立降低蛋白合成。这就提出了细菌差异表达伴侣蛋白和伴侣蛋白的可能性。我们现在报道鼠伤寒沙门氏菌对细胞质Mg2+饥饿的反应是增加dnaK的mRNA量,同时减少tf编码基因tig和j结构域共伴侣基因dnaJ和djlA的mRNA量。这种差异策略需要Mg2+稳态和毒力PhoP的主调控因子,通过降低ATP浓度来增加dnaK mRNA的数量,从而阻碍负责dnaK转录的替代sigma因子RpoH的蛋白水解。我们还发现DnaK对RpoH蛋白和RpoH依赖性转录物施加负反馈,而不依赖于j结构域的合作伙伴。因此,细菌根据特定的应激干扰蛋白稳态,协调或差异地表达伴侣蛋白和伴侣蛋白。重要意义分子伴侣通常需要伴侣来折叠蛋白质并防止蛋白质聚集,因此相应的基因被协调表达。我们现在已经确定了一种感染相关的应激条件,在这种条件下,尽管属于同一操纵子,但指定伴侣dna ak和伴侣DnaJ的基因却存在差异表达。这种差异策略需要在病原体肠道沙门氏菌血清型鼠伤寒沙门氏菌中进行Mg2+稳态和毒力的主调控。此外,这可能反映了沙门氏菌需要dnaK而不是j结构域cochaperone编码基因来抵抗细胞质Mg2+饥饿,并且只在需要时表达基因。因此,影响蛋白质稳态的特定条件决定了分子伴侣和辅伴侣的坐标与差异表达。
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
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
×
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