Signal Transduction Network Principles Underlying Bacterial Collective Behaviors.

IF 8.5 1区 生物学 Q1 MICROBIOLOGY Annual review of microbiology Pub Date : 2022-09-08 DOI:10.1146/annurev-micro-042922-122020
Andrew A Bridges, Jojo A Prentice, Ned S Wingreen, Bonnie L Bassler
{"title":"Signal Transduction Network Principles Underlying Bacterial Collective Behaviors.","authors":"Andrew A Bridges,&nbsp;Jojo A Prentice,&nbsp;Ned S Wingreen,&nbsp;Bonnie L Bassler","doi":"10.1146/annurev-micro-042922-122020","DOIUrl":null,"url":null,"abstract":"<p><p>Bacteria orchestrate collective behaviors and accomplish feats that would be unsuccessful if carried out by a lone bacterium. Processes undertaken by groups of bacteria include bioluminescence, biofilm formation, virulence factor production, and release of public goods that are shared by the community. Collective behaviors are controlled by signal transduction networks that integrate sensory information and transduce the information internally. Here, we discuss network features and mechanisms that, even in the face of dramatically changing environments, drive precise execution of bacterial group behaviors. We focus on representative quorum-sensing and second-messenger cyclic dimeric GMP (c-di-GMP) signal relays. We highlight ligand specificity versus sensitivity, how small-molecule ligands drive discrimination of kin versus nonkin, signal integration mechanisms, single-input sensory systems versus coincidence detectors, and tuning of input-output dynamics via feedback regulation. We summarize how different features of signal transduction systems allow groups of bacteria to successfully interpret and collectively react to dynamically changing environments.</p>","PeriodicalId":7946,"journal":{"name":"Annual review of microbiology","volume":"76 ","pages":"235-257"},"PeriodicalIF":8.5000,"publicationDate":"2022-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463083/pdf/nihms-1790607.pdf","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annual review of microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1146/annurev-micro-042922-122020","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 8

Abstract

Bacteria orchestrate collective behaviors and accomplish feats that would be unsuccessful if carried out by a lone bacterium. Processes undertaken by groups of bacteria include bioluminescence, biofilm formation, virulence factor production, and release of public goods that are shared by the community. Collective behaviors are controlled by signal transduction networks that integrate sensory information and transduce the information internally. Here, we discuss network features and mechanisms that, even in the face of dramatically changing environments, drive precise execution of bacterial group behaviors. We focus on representative quorum-sensing and second-messenger cyclic dimeric GMP (c-di-GMP) signal relays. We highlight ligand specificity versus sensitivity, how small-molecule ligands drive discrimination of kin versus nonkin, signal integration mechanisms, single-input sensory systems versus coincidence detectors, and tuning of input-output dynamics via feedback regulation. We summarize how different features of signal transduction systems allow groups of bacteria to successfully interpret and collectively react to dynamically changing environments.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
细菌集体行为背后的信号转导网络原理。
细菌协调集体行为,完成了如果由一个单独的细菌完成是不可能成功的壮举。细菌群进行的过程包括生物发光、生物膜形成、毒力因子的产生和社区共享的公共产品的释放。集体行为受信号转导网络控制,信号转导网络整合感官信息并在内部传递信息。在这里,我们讨论了网络特征和机制,即使面对急剧变化的环境,也能驱动细菌群体行为的精确执行。我们重点研究了具有代表性的群体感应和第二信使环二聚GMP (c-di-GMP)信号继电器。我们强调配体的特异性与敏感性,小分子配体如何驱动近亲与非近亲的区分,信号整合机制,单输入感觉系统与巧合检测器,以及通过反馈调节的输入-输出动态的调整。我们总结了信号转导系统的不同特征如何使细菌群成功地解释并集体对动态变化的环境做出反应。
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 去求助
来源期刊
Annual review of microbiology
Annual review of microbiology 生物-微生物学
CiteScore
18.10
自引率
0.00%
发文量
37
期刊介绍: Annual Review of Microbiology is a Medical and Microbiology Journal and published by Annual Reviews Inc. The Annual Review of Microbiology, in publication since 1947, covers significant developments in the field of microbiology, encompassing bacteria, archaea, viruses, and unicellular eukaryotes. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license. The Impact Factor of Annual Review of Microbiology is 10.242 (2024) Impact factor. The Annual Review of Microbiology Journal is Indexed with Pubmed, Scopus, UGC (University Grants Commission).
期刊最新文献
Understanding the Diversity, Evolution, Ecology, and Applications of Mycoviruses. Mechanisms Underlying Ophiocordyceps Infection and Behavioral Manipulation of Ants: Unique or Ubiquitous? Cyclic Diguanylate in the Wild: Roles During Plant and Animal Colonization How Bacteria Establish and Maintain Outer Membrane Lipid Asymmetry Dimethylsulfoniopropionate (DMSP): From Biochemistry to Global Ecological Significance.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1