Natural silencing of quorum-sensing activity protects Vibrio parahaemolyticus from lysis by an autoinducer-detecting phage.

IF 4.5 2区 生物学 Q1 Agricultural and Biological Sciences
Olivia P Duddy, Justin E Silpe, Chenyi Fei, Bonnie L Bassler
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引用次数: 0

Abstract

Quorum sensing (QS) is a chemical communication process that bacteria use to track population density and orchestrate collective behaviors. QS relies on the production, accumulation, and group-wide detection of extracellular signal molecules called autoinducers. Vibriophage 882 (phage VP882), a bacterial virus, encodes a homolog of the Vibrio QS receptor-transcription factor, called VqmA, that monitors the Vibrio QS autoinducer DPO. Phage VqmA binds DPO at high host-cell density and activates transcription of the phage gene qtip. Qtip, an antirepressor, launches the phage lysis program. Phage-encoded VqmA when bound to DPO also manipulates host QS by activating transcription of the host gene vqmR. VqmR is a small RNA that controls downstream QS target genes. Here, we sequence Vibrio parahaemolyticus strain O3:K6 882, the strain from which phage VP882 was initially isolated. The chromosomal region normally encoding vqmR and vqmA harbors a deletion encompassing vqmR and a portion of the vqmA promoter, inactivating that QS system. We discover that V. parahaemolyticus strain O3:K6 882 is also defective in its other QS systems, due to a mutation in luxO, encoding the central QS transcriptional regulator LuxO. Both the vqmR-vqmA and luxO mutations lock V. parahaemolyticus strain O3:K6 882 into the low-cell density QS state. Reparation of the QS defects in V. parahaemolyticus strain O3:K6 882 promotes activation of phage VP882 lytic gene expression and LuxO is primarily responsible for this effect. Phage VP882-infected QS-competent V. parahaemolyticus strain O3:K6 882 cells lyse more rapidly and produce more viral particles than the QS-deficient parent strain. We propose that, in V. parahaemolyticus strain O3:K6 882, constitutive maintenance of the low-cell density QS state suppresses the launch of the phage VP882 lytic cascade, thereby protecting the bacterial host from phage-mediated lysis.

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群体感应活性的自然沉默保护副溶血性弧菌免受自诱导剂检测噬菌体的裂解。
群体感应(QS)是细菌用来追踪种群密度和协调集体行为的一种化学通讯过程。QS依赖于被称为自诱导剂的细胞外信号分子的产生、积累和群体范围的检测。Vibriophage 882(噬菌体VP882)是一种细菌病毒,编码一种名为VqmA的Vibrio QS受体转录因子的同源物,该因子可监测Vibrio QS自诱导剂DPO。噬菌体VqmA以高宿主细胞密度结合DPO,激活噬菌体基因qtip的转录。Qtip是一种抗抑制因子,启动噬菌体裂解程序。当与DPO结合时,噬菌体编码的VqmA也通过激活宿主基因vqmR的转录来操纵宿主QS。VqmR是一种控制下游QS靶基因的小RNA。在这里,我们对最初分离噬菌体VP882的副溶血性弧菌O3:K6 882进行了测序。通常编码vqmR和vqmA的染色体区域含有一个包含vqmR和部分vqmA启动子的缺失,使该QS系统失活。我们发现副溶血性弧菌菌株O3:K6 882在其其他QS系统中也存在缺陷,这是由于编码QS中心转录调节因子luxO的luxO突变。vqmR-vqmA和luxO突变均将副溶血性弧菌O3:K6 882锁定在低细胞密度的QS状态。副溶血性弧菌O3:K6 882的QS缺陷修复促进了噬菌体VP882裂解基因表达的激活,LuxO是这一作用的主要原因。噬菌体vp882感染的QS-competent副溶血性弧菌O3:K6 882细胞比缺乏qs的亲本株裂解速度更快,产生更多的病毒颗粒。我们认为,在副溶血性弧菌O3:K6 882菌株中,低细胞密度QS状态的组成性维持抑制了噬菌体VP882裂解级联的启动,从而保护细菌宿主免受噬菌体介导的裂解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS Genetics
PLoS Genetics 生物-遗传学
CiteScore
8.10
自引率
2.20%
发文量
438
审稿时长
1 months
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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