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QsrO:铜绿假单胞菌群体感应和毒力的新型调节因子。

QsrO a novel regulator of quorum-sensing and virulence in Pseudomonas aeruginosa.

作者信息

Köhler Thilo, Ouertatani-Sakouhi Hajer, Cosson Pierre, van Delden Christian

机构信息

Departement of Microbiology and Molecular Medicine, University of Geneva, Geneva, Switzerland ; Service of Infectious Diseases, University Hospitals Geneva, Geneva, Switzerland.

Department of Physiology and Metabolism, University of Geneva, Geneva, Switzerland.

出版信息

PLoS One. 2014 Feb 13;9(2):e87814. doi: 10.1371/journal.pone.0087814. eCollection 2014.

Abstract

In Pseudomonas aeruginosa, the production of many secreted virulence factors is controlled by a quorum-sensing (QS) circuit, constituted of transcriptional activators (LasR, RhlR, PqsR) and their cognate signaling molecules (3-oxo-C12-HSL, C4-HSL, PQS). QS is a cooperative behavior that is beneficial to a population but can be exploited by "QS-cheaters", individuals which do not respond to the QS-signal, but can use public goods produced by QS-cooperators. In order to identify QS-deficient clones we designed a genetic screening based on a lasB-lacZ fusion. We isolated one clone (PT1617) deficient in QS-dependent gene expression and virulence factor production despite wild type lasR, rhlR and pqsR alleles. Whole genome sequencing of PT1617 revealed a 3,552 bp deletion encompassing ORFs PA2228-PA2229-PA2230 and the pslA gene. However, complementation of PT1617 by plasmid-encoded copies of these ORFs, did not restore QS. Unexpectedly, gene expression levels of ORFs PA2228, PA2227 (vqsM) and PA2222, located adjacent to the deletion, were 10 to 100 fold higher in mutant PT1617 than in PAO1. When expressed from a constitutive promoter on a plasmid, PA2226, alone was found to be sufficient to confer a QS-negative phenotype on PAO1 as well as on PA14. Co-expression of PA2226 and PA2225 in PAO1 further prevented induction of the type III secretion system. In summary, we have identified a novel genetic locus including ORF2226 termed qsrO (QS-repressing ORF), capable of down-regulating all three known QS-systems in P. aeruginosa.

摘要

在铜绿假单胞菌中,许多分泌型毒力因子的产生受群体感应(QS)回路控制,该回路由转录激活因子(LasR、RhlR、PqsR)及其同源信号分子(3-氧代-C12-HSL、C4-HSL、PQS)组成。群体感应是一种对群体有益的合作行为,但可能被“QS作弊者”利用,即那些不响应QS信号但能利用QS合作者产生的公共物品的个体。为了鉴定缺乏群体感应的克隆,我们基于lasB-lacZ融合设计了一种遗传筛选方法。我们分离出一个克隆(PT1617),尽管其lasR、rhlR和pqsR等位基因是野生型,但该克隆在群体感应依赖性基因表达和毒力因子产生方面存在缺陷。PT1617的全基因组测序揭示了一个3552 bp的缺失,该缺失涵盖了开放阅读框PA2228-PA2229-PA2230和pslA基因。然而,用这些开放阅读框的质粒编码拷贝对PT1617进行互补,并不能恢复群体感应。出乎意料的是,位于缺失区域附近的开放阅读框PA2228、PA2227(vqsM)和PA2222在突变体PT1617中的基因表达水平比在PAO1中高10到100倍。当从质粒上的组成型启动子表达时,单独的PA2226就足以赋予PAO1和PA14群体感应阴性表型。在PAO1中PA2226和PA2225的共表达进一步阻止了III型分泌系统的诱导。总之,我们鉴定出了一个新的遗传位点,包括称为qsrO(群体感应抑制开放阅读框)的开放阅读框2226,它能够下调铜绿假单胞菌中所有三种已知的群体感应系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e03/3923755/1061f931e6d7/pone.0087814.g001.jpg

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