群体感应调节珊瑚病原体珊瑚弧菌的毒力因子。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Victoria N Lydick, Shir Mass, Robert Pepin, Ram Podicheti, Emra Klempic, Douglas B Rusch, Blake Ushijima, Laura C Brown, Dor Salomon, Julia C van Kessel
{"title":"群体感应调节珊瑚病原体珊瑚弧菌的毒力因子。","authors":"Victoria N Lydick, Shir Mass, Robert Pepin, Ram Podicheti, Emra Klempic, Douglas B Rusch, Blake Ushijima, Laura C Brown, Dor Salomon, Julia C van Kessel","doi":"10.1128/aem.01143-24","DOIUrl":null,"url":null,"abstract":"<p><p>The bacterial pathogen <i>Vibrio coralliilyticus</i> causes disease in coral species worldwide. The mechanisms of <i>V. coralliilyticus</i> coral colonization, coral microbiome interactions, and virulence factor production are understudied. In other model <i>Vibrio</i> species, virulence factors like biofilm formation, toxin secretion, and protease production are controlled through a density-dependent communication system called quorum sensing (QS). Comparative genomics indicated that <i>V. coralliilyticus</i> genomes share high sequence identity for most of the QS signaling and regulatory components identified in other <i>Vibrio</i> species. Here, we identify an active QS signaling pathway in two <i>V. coralliilyticus</i> strains with distinct infection etiologies: type strain BAA-450 and coral isolate OCN008. In <i>V. coralliilyticus</i>, the inter-species AI-2 autoinducer signaling pathway in both strains controls expression of the master QS transcription factor and LuxR/HapR homolog VcpR to regulate >300 genes, including protease production, biofilm formation, and two conserved type VI secretion systems (T6SSs). Activation of T6SS1 by QS results in the secretion of effectors and enables interbacterial competition and killing of prey bacteria. We conclude that the QS system in <i>V. coralliilyticus</i> is functional and controls the expression of genes involved in relevant bacterial behaviors typically associated with host infection.IMPORTANCE<i>Vibrio coralliilyticus</i> infects many marine organisms, including multiple species of corals, and is a primary causative agent of tissue loss diseases and bacterial-induced bleaching. Here, we investigated a common cell-cell communication mechanism called quorum sensing, which is known to be intimately connected to virulence in other <i>Vibrio</i> species. Our genetic and chemical studies of <i>V. coralliilyticus</i> quorum sensing uncovered an active pathway that directly regulates the following key virulence factors: proteases, biofilms, and secretion systems. These findings connect bacterial signaling in communities to the infection of corals, which may lead to novel treatments and earlier diagnoses of coral diseases in reefs.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0114324"},"PeriodicalIF":3.9000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quorum sensing regulates virulence factors in the coral pathogen <i>Vibrio coralliilyticus</i>.\",\"authors\":\"Victoria N Lydick, Shir Mass, Robert Pepin, Ram Podicheti, Emra Klempic, Douglas B Rusch, Blake Ushijima, Laura C Brown, Dor Salomon, Julia C van Kessel\",\"doi\":\"10.1128/aem.01143-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The bacterial pathogen <i>Vibrio coralliilyticus</i> causes disease in coral species worldwide. The mechanisms of <i>V. coralliilyticus</i> coral colonization, coral microbiome interactions, and virulence factor production are understudied. In other model <i>Vibrio</i> species, virulence factors like biofilm formation, toxin secretion, and protease production are controlled through a density-dependent communication system called quorum sensing (QS). Comparative genomics indicated that <i>V. coralliilyticus</i> genomes share high sequence identity for most of the QS signaling and regulatory components identified in other <i>Vibrio</i> species. Here, we identify an active QS signaling pathway in two <i>V. coralliilyticus</i> strains with distinct infection etiologies: type strain BAA-450 and coral isolate OCN008. In <i>V. coralliilyticus</i>, the inter-species AI-2 autoinducer signaling pathway in both strains controls expression of the master QS transcription factor and LuxR/HapR homolog VcpR to regulate >300 genes, including protease production, biofilm formation, and two conserved type VI secretion systems (T6SSs). Activation of T6SS1 by QS results in the secretion of effectors and enables interbacterial competition and killing of prey bacteria. We conclude that the QS system in <i>V. coralliilyticus</i> is functional and controls the expression of genes involved in relevant bacterial behaviors typically associated with host infection.IMPORTANCE<i>Vibrio coralliilyticus</i> infects many marine organisms, including multiple species of corals, and is a primary causative agent of tissue loss diseases and bacterial-induced bleaching. Here, we investigated a common cell-cell communication mechanism called quorum sensing, which is known to be intimately connected to virulence in other <i>Vibrio</i> species. Our genetic and chemical studies of <i>V. coralliilyticus</i> quorum sensing uncovered an active pathway that directly regulates the following key virulence factors: proteases, biofilms, and secretion systems. These findings connect bacterial signaling in communities to the infection of corals, which may lead to novel treatments and earlier diagnoses of coral diseases in reefs.</p>\",\"PeriodicalId\":8002,\"journal\":{\"name\":\"Applied and Environmental Microbiology\",\"volume\":\" \",\"pages\":\"e0114324\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-01-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied and Environmental Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/aem.01143-24\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.01143-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

细菌病原体珊瑚弧菌在世界各地的珊瑚物种中引起疾病。珊瑚弧菌的珊瑚定植、珊瑚微生物群相互作用和毒力因子产生的机制尚未得到充分研究。在其他模式弧菌物种中,毒力因子如生物膜形成、毒素分泌和蛋白酶产生是通过一种称为群体感应(quorum sensing, QS)的依赖于密度的通信系统来控制的。比较基因组学表明,在其他弧菌中鉴定出的大部分QS信号和调控成分,coralliilyticus基因组具有较高的序列一致性。在这里,我们在两种不同感染病原的珊瑚弧菌中发现了一个活跃的QS信号通路:型菌株BAA-450和珊瑚分离物OCN008。在coralliilyticus中,两种菌株的种间AI-2自诱导剂信号通路控制主QS转录因子和LuxR/HapR同源VcpR的表达,调控bbb300基因,包括蛋白酶产生、生物膜形成和两个保守的VI型分泌系统(t6ss)。QS激活T6SS1导致效应物的分泌,使细菌间竞争并杀死猎物细菌。我们得出结论,珊瑚弧菌的QS系统是功能性的,并控制着与宿主感染相关的细菌行为相关的基因的表达。珊瑚弧菌感染许多海洋生物,包括多种珊瑚,是组织丢失疾病和细菌引起的白化的主要病原体。在这里,我们研究了一种称为群体感应的常见细胞-细胞通信机制,已知它与其他弧菌物种的毒力密切相关。我们对珊瑚弧菌群体感应的遗传和化学研究发现了一个直接调节以下关键毒力因子的活性途径:蛋白酶、生物膜和分泌系统。这些发现将群落中的细菌信号与珊瑚感染联系起来,这可能会导致新的治疗方法和珊瑚礁疾病的早期诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quorum sensing regulates virulence factors in the coral pathogen Vibrio coralliilyticus.

The bacterial pathogen Vibrio coralliilyticus causes disease in coral species worldwide. The mechanisms of V. coralliilyticus coral colonization, coral microbiome interactions, and virulence factor production are understudied. In other model Vibrio species, virulence factors like biofilm formation, toxin secretion, and protease production are controlled through a density-dependent communication system called quorum sensing (QS). Comparative genomics indicated that V. coralliilyticus genomes share high sequence identity for most of the QS signaling and regulatory components identified in other Vibrio species. Here, we identify an active QS signaling pathway in two V. coralliilyticus strains with distinct infection etiologies: type strain BAA-450 and coral isolate OCN008. In V. coralliilyticus, the inter-species AI-2 autoinducer signaling pathway in both strains controls expression of the master QS transcription factor and LuxR/HapR homolog VcpR to regulate >300 genes, including protease production, biofilm formation, and two conserved type VI secretion systems (T6SSs). Activation of T6SS1 by QS results in the secretion of effectors and enables interbacterial competition and killing of prey bacteria. We conclude that the QS system in V. coralliilyticus is functional and controls the expression of genes involved in relevant bacterial behaviors typically associated with host infection.IMPORTANCEVibrio coralliilyticus infects many marine organisms, including multiple species of corals, and is a primary causative agent of tissue loss diseases and bacterial-induced bleaching. Here, we investigated a common cell-cell communication mechanism called quorum sensing, which is known to be intimately connected to virulence in other Vibrio species. Our genetic and chemical studies of V. coralliilyticus quorum sensing uncovered an active pathway that directly regulates the following key virulence factors: proteases, biofilms, and secretion systems. These findings connect bacterial signaling in communities to the infection of corals, which may lead to novel treatments and earlier diagnoses of coral diseases in reefs.

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
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
×
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