Response of Escherichia coli chemotaxis pathway to pyrimidine deoxyribonucleosides.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Malay Shah, Wenhao Xu, Victor Sourjik
{"title":"Response of <i>Escherichia coli</i> chemotaxis pathway to pyrimidine deoxyribonucleosides.","authors":"Malay Shah, Wenhao Xu, Victor Sourjik","doi":"10.1128/spectrum.02048-25","DOIUrl":null,"url":null,"abstract":"<p><p>Nucleosides are essential components of all living cells. Bacteria use salvage pathways to import nucleosides from their environment and to utilize them for nucleic acid biosynthesis, but also as alternative sources of carbon, nitrogen and energy. Motile bacteria commonly show chemoattraction towards nutritionally valuable compounds, and in this work, we demonstrate that the chemotaxis pathway of <i>Escherichia coli</i> exhibits specific attractant response to pyrimidine nucleosides. The most sensitive response, in the sub-micromolar range, was observed for pyrimidine deoxyribonucleosides, thymidine (deoxythymidine) and deoxycytidine. In contrast, pyrimidine ribonucleosides elicited weaker and less sensitive response, and no response to pyrimidine nucleobases was observed in the micromolar range of concentrations. Furthermore, no response was observed to tested purine nucleosides or nucleobases. Our subsequent analysis revealed that the pathway response to pyrimidine deoxyribonucleosides is mediated by the minor <i>E. coli</i> chemoreceptor Tap, whereas the response to the ribonucleoside uridine relies on a different mechanism. The observed narrow dynamic range of this response indicates that sensing of deoxyribonucleosides is indirect, likely via an unknown periplasmic binding protein that interacts with Tap.IMPORTANCEChemotactic behavior is highly important for bacterial ecology, enabling motile bacteria to locate environments that are optimal for growth, and it became a paradigm for bacterial environmental sensing and signal transduction. However, even for model organisms, the spectrum of stimuli sensed by the chemotaxis pathway is not fully known, which limits our understanding of the physiological and ecological relevance of the chemotactic behavior. Here, we identified pyrimidine deoxyribonucleosides as a novel and highly specific class of chemoeffector metabolites for <i>Escherichia coli</i>, the most studied chemotaxis model. Our work expands the number of bacterial species that exhibit chemotactic responses to nucleotide derivatives, strengthening the notion that pyrimidines and purines constitute a highly important class of chemoeffectors for many bacteria.</p>","PeriodicalId":18670,"journal":{"name":"Microbiology spectrum","volume":" ","pages":"e0204825"},"PeriodicalIF":3.8000,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology spectrum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/spectrum.02048-25","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Nucleosides are essential components of all living cells. Bacteria use salvage pathways to import nucleosides from their environment and to utilize them for nucleic acid biosynthesis, but also as alternative sources of carbon, nitrogen and energy. Motile bacteria commonly show chemoattraction towards nutritionally valuable compounds, and in this work, we demonstrate that the chemotaxis pathway of Escherichia coli exhibits specific attractant response to pyrimidine nucleosides. The most sensitive response, in the sub-micromolar range, was observed for pyrimidine deoxyribonucleosides, thymidine (deoxythymidine) and deoxycytidine. In contrast, pyrimidine ribonucleosides elicited weaker and less sensitive response, and no response to pyrimidine nucleobases was observed in the micromolar range of concentrations. Furthermore, no response was observed to tested purine nucleosides or nucleobases. Our subsequent analysis revealed that the pathway response to pyrimidine deoxyribonucleosides is mediated by the minor E. coli chemoreceptor Tap, whereas the response to the ribonucleoside uridine relies on a different mechanism. The observed narrow dynamic range of this response indicates that sensing of deoxyribonucleosides is indirect, likely via an unknown periplasmic binding protein that interacts with Tap.IMPORTANCEChemotactic behavior is highly important for bacterial ecology, enabling motile bacteria to locate environments that are optimal for growth, and it became a paradigm for bacterial environmental sensing and signal transduction. However, even for model organisms, the spectrum of stimuli sensed by the chemotaxis pathway is not fully known, which limits our understanding of the physiological and ecological relevance of the chemotactic behavior. Here, we identified pyrimidine deoxyribonucleosides as a novel and highly specific class of chemoeffector metabolites for Escherichia coli, the most studied chemotaxis model. Our work expands the number of bacterial species that exhibit chemotactic responses to nucleotide derivatives, strengthening the notion that pyrimidines and purines constitute a highly important class of chemoeffectors for many bacteria.

大肠杆菌趋化途径对嘧啶脱氧核糖核苷的响应。
核苷是所有活细胞的基本成分。细菌利用回收途径从环境中进口核苷,并利用它们进行核酸生物合成,同时也作为碳、氮和能量的替代来源。运动细菌通常对有营养价值的化合物表现出化学吸引,在这项工作中,我们证明了大肠杆菌的趋化途径对嘧啶核苷表现出特定的引诱反应。在亚微摩尔范围内,对嘧啶脱氧核糖核苷、胸腺嘧啶(脱氧胸腺嘧啶)和脱氧胞苷的反应最为敏感。相比之下,嘧啶核苷引起的反应较弱,敏感性较低,在微摩尔浓度范围内对嘧啶核碱基没有反应。此外,对测试的嘌呤核苷或核碱基没有反应。我们随后的分析表明,对嘧啶脱氧核糖核苷的通路反应是由次要的大肠杆菌化学受体Tap介导的,而对核糖核苷尿苷的反应依赖于不同的机制。观察到的这种反应的窄动态范围表明,对脱氧核糖核苷的感知是间接的,可能是通过一种未知的与Tap相互作用的质周结合蛋白。趋化行为对细菌生态学非常重要,它使活动细菌能够找到最适合生长的环境,并成为细菌环境感知和信号转导的范例。然而,即使对于模式生物,趋化途径感知的刺激谱也不完全清楚,这限制了我们对趋化行为的生理和生态相关性的理解。在这里,我们发现嘧啶脱氧核糖核苷是大肠杆菌的一种新的和高度特异性的化学效应代谢物,大肠杆菌是研究最多的趋化模型。我们的工作扩大了对核苷酸衍生物表现出趋化反应的细菌种类的数量,加强了嘧啶和嘌呤构成许多细菌非常重要的一类化学效应物的概念。
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
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
×
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:604180095
Book学术官方微信