The relationship between pqs gene expression and acylhomoserine lactone signaling in Pseudomonas aeruginosa.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY Journal of Bacteriology Pub Date : 2024-10-24 Epub Date: 2024-09-05 DOI:10.1128/jb.00138-24
Martín P Soto-Aceves, Nicole E Smalley, Amy L Schaefer, E Peter Greenberg
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Abstract

The opportunistic pathogen Pseudomonas aeruginosa has complex quorum sensing (QS) circuitry, which involves two acylhomoserine lactone (AHL) systems, the LasI AHL synthase and LasR AHL-dependent transcriptional activator system and the RhlI AHL synthase-RhlR AHL-responsive transcriptional activator. There is also a quinoline signaling system [the Pseudomonas quinolone signal (PQS) system]. Although there is a core set of genes regulated by the AHL circuits, there is strain-to-strain variation in the non-core QS regulon. A size reduction of the QS regulon occurs in laboratory evolution experiments with the model strain PAO1. We used transcriptomics to test the hypothesis that reductive evolution in the PAO1 QS regulon can in large part be explained by a null mutation in pqsR, the gene encoding the transcriptional activator of the pqs operon. We found that PqsR had very little influence on the AHL QS regulon. This was a surprising finding because the last gene in the PqsR-dependent pqs operon, pqsE, codes for a protein, which physically interacts with RhlR, and this interaction is required for RhlR-dependent activation of some genes. We used comparative transcriptomics to examine the influence of a pqsE mutation on the QS regulon and identified only three transcripts, which were strictly dependent on PqsE. By using reporter constructs, we showed that the PqsE influence on other genes was dependent on experimental conditions and we have gained some insight about those conditions. This work adds to our understanding of the plasticity of the P. aeruginosa QS regulon and to the role PqsE plays in RhlR-dependent gene activation.IMPORTANCEOver many generations of growth in certain conditions, Pseudomonas aeruginosa undergoes a large reductive evolution in the number of genes activated by quorum sensing. Here, we rule out one plausible route of the reductive evolution: that a mutation in a transcriptional activator PqsR or the PqsR activation of pqsE, which codes for a chaperone for the quorum sensing signal-responsive transcription factor RhlR, explains the finding. We further provide information about the influence of PqsR and PqsE on quorum sensing in P. aeruginosa.

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铜绿假单胞菌中 pqs 基因表达与酰基高丝氨酸内酯信号之间的关系。
机会性病原体铜绿假单胞菌(Pseudomonas aeruginosa)具有复杂的法定量感应(QS)回路,其中涉及两个酰基高丝氨酸内酯(AHL)系统,即 LasI AHL 合成酶和 LasR AHL 依赖性转录激活因子系统以及 RhlI AHL 合成酶-RhlR AHL 响应性转录激活因子。还有一个喹啉信号系统[假单胞菌喹诺酮信号(PQS)系统]。虽然有一组核心基因受 AHL 电路调控,但非核心的 QS 调节子存在菌株间的差异。在用模式菌株 PAO1 进行的实验室进化实验中,QS 调节子的规模有所缩小。我们利用转录组学检验了一个假设,即 PAO1 QS 调节子的还原进化在很大程度上可以用 pqsR(编码 pqs 操作子转录激活子的基因)的空突变来解释。我们发现 PqsR 对 AHL QS 调节子的影响很小。这是一个令人惊讶的发现,因为依赖 PqsR 的 pqs 操作子中的最后一个基因 pqsE 编码一种蛋白质,它与 RhlR 有物理相互作用,而这种相互作用是某些基因依赖 RhlR 激活所必需的。我们利用比较转录组学研究了 pqsE 突变对 QS 调控子的影响,发现只有三个转录本严格依赖于 PqsE。这项工作加深了我们对铜绿假单胞菌 QS 调节子的可塑性以及 PqsE 在 RhlR 依赖性基因激活中所起作用的理解。在此,我们排除了还原进化的一种可能途径:转录激活因子 PqsR 的突变或 PqsR 对 pqsE 的激活(pqsE 编码法定量感应信号响应转录因子 RhlR 的伴侣蛋白)可以解释这一发现。我们进一步提供了有关 PqsR 和 PqsE 对铜绿微囊藻法定量感应的影响的信息。
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
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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