Viducic Darija, Murakami Keiji, Amoh Takashi, Ono Tsuneko, Miyake Yoichiro
Department of Oral Microbiology, Institute of Biomedical Sciences, Tokushima University Graduate School, Kuramoto-cho 3-18-15, Tokushima 770-8504, Japan; Department of Molecular Microbiology, Institute of Health Biosciences, Tokushima University Graduate School, Kuramoto-cho 3-18-15, Tokushima 770-8509, Japan.
Department of Oral Microbiology, Institute of Biomedical Sciences, Tokushima University Graduate School, Kuramoto-cho 3-18-15, Tokushima 770-8504, Japan.
Res Microbiol. 2017 Jun;168(5):450-460. doi: 10.1016/j.resmic.2017.02.007. Epub 2017 Mar 2.
Pseudomonas aeruginosa coordinates its response to environmental conditions through activation of a quorum sensing (QS) system. In this study, we investigated the regulatory interaction between the QS transcriptional regulator VqsR and the Pseudomonas quinolone signal (PQS) through integration of sigma factor RpoS, and we addressed whether one of the pathways controlling carbapenem tolerance can be attributed to VqsR. We demonstrate that vqsR expression at the transcriptional level is regulated by pqsA, pqsR, and pqsE. Assessment of the transcriptional expression of vqsR, lasI, rhlI, and qscR in ΔpqsA and ΔpqsAΔrpoS mutants provided insight into pqsA- and rpoS-dependent regulation of vqsR and vqsR-controlled genes. Exogenously supplemented PQS reversed expression of vqsR and vqsR-controlled genes in the ΔpqsA mutant to wild-type levels, but failed to increase expression levels of lasI and qscR in the ΔpqsAΔrpoS mutant to levels observed in wild-type PAO1. The ΔvqsR mutant showed reduced survival when challenged with carbapenems compared to wild-type PAO1. Introduction of a pqsA mutation into the ΔvqsR mutant completely abolished its carbapenem-sensitive phenotype. We conclude that a regulatory link between PQS and vqsR exists, and that RpoS is important in their interaction. We also demonstrate that VqsR affects carbapenem tolerance.
铜绿假单胞菌通过激活群体感应(QS)系统来协调其对环境条件的反应。在本研究中,我们通过整合σ因子RpoS,研究了QS转录调节因子VqsR与铜绿假单胞菌喹诺酮信号(PQS)之间的调节相互作用,并探讨了控制碳青霉烯耐受性的途径之一是否可归因于VqsR。我们证明,vqsR在转录水平的表达受pqsA、pqsR和pqsE的调控。对ΔpqsA和ΔpqsAΔrpoS突变体中vqsR、lasI、rhlI和qscR转录表达的评估,为pqsA和rpoS对vqsR及vqsR控制基因的依赖性调节提供了深入了解。外源补充PQS可使ΔpqsA突变体中vqsR和vqsR控制基因的表达恢复到野生型水平,但未能将ΔpqsAΔrpoS突变体中lasI和qscR的表达水平提高到野生型PAO1中观察到的水平。与野生型PAO1相比,ΔvqsR突变体在用碳青霉烯类药物攻击时存活率降低。在ΔvqsR突变体中引入pqsA突变完全消除了其对碳青霉烯类药物敏感的表型。我们得出结论,PQS与vqsR之间存在调节联系,且RpoS在它们的相互作用中很重要。我们还证明,VqsR影响碳青霉烯耐受性。