MvfR Shapes Pseudomonas aeruginosa Interactions in Polymicrobial Contexts: Implications for Targeted Quorum-Sensing Inhibition.

IF 5.1 2区 生物学 Q2 CELL BIOLOGY
Cells Pub Date : 2025-05-20 DOI:10.3390/cells14100744
Kelsey M Wheeler, Myung Whan Oh, Julianna Fusco, Aishlinn Mershon, Erin Kim, Antonia De Oliveira, Laurence G Rahme
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引用次数: 0

Abstract

Infections often occur in complex niches consisting of multiple bacteria. Despite the increasing awareness, there is a fundamental gap in understanding which interactions govern microbial community composition. Pseudomonas aeruginosa is frequently isolated from monomicrobial and polymicrobial human infections. This pathogen forms polymicrobial infections with other ESKAPEE pathogens and defies eradication by conventional therapies. By analyzing the competition within co-cultures of P. aeruginosa and representative secondary pathogens that commonly co-infect patients, we demonstrate the antagonism of P. aeruginosa against other ESKAPEE pathogens and the contribution of this pathogen's multiple quorum-sensing (QS) systems in these interactions. QS is a highly conserved bacterial cell-to-cell communication mechanism that coordinates collective gene expressions at the population level, and it is also involved in P. aeruginosa virulence. Using a collection of P. aeruginosa QS mutants of the three major systems, LasR/LasI, MvfR/PqsABCDE, and RhlR/RhlI, and mutants of several QS-regulated functions, we reveal that MvfR and, to a lesser extent, LasR and RhlR, control competition between P. aeruginosa and other microbes, possibly through their positive impact on pyoverdine, pyochelin, and phenazine genes. We show that MvfR inhibition alters competitive interspecies interactions and preserves the coexistence of P. aeruginosa with the ESKAPEE pathogens tested while disarming the pathogens' ability to form biofilm and adhere to lung epithelial cells. Our results highlight the role of MvfR inhibition in modulating microbial competitive interactions across multiple species, while simultaneously attenuating virulence traits. These findings reveal the complexity and importance of QS in interspecies interactions and underscore the impact of the anti-virulence approach in microbial ecology and its importance for treating polymicrobial infections.

MvfR形状铜绿假单胞菌在多微生物环境中的相互作用:对目标群体感应抑制的影响。
感染通常发生在由多种细菌组成的复杂生态位中。尽管越来越多的认识,有一个根本的理解差距,相互作用支配微生物群落组成。铜绿假单胞菌经常从单微生物和多微生物人类感染中分离出来。这种病原体与其他ESKAPEE病原体形成多微生物感染,无法通过传统疗法根除。通过分析铜绿假单胞菌(P. aeruginosa)和通常共同感染患者的代表性继发病原体在共培养中的竞争,我们证明了铜绿假单胞菌(P. aeruginosa)对其他ESKAPEE病原体的拮抗作用,以及该病原体的多群体感应(QS)系统在这些相互作用中的作用。QS是一种高度保守的细菌细胞间通讯机制,在群体水平上协调集体基因表达,也参与了P. aeruginosa的毒力。通过对铜绿假单胞菌QS中LasR/LasI、MvfR/PqsABCDE、RhlR/RhlI三种主要系统的突变体以及几种具有QS调控功能的突变体的分析,我们发现MvfR以及LasR和RhlR可能通过对pyoverdine、pyochelin和phenazine基因的积极影响,控制了铜绿假单胞菌与其他微生物之间的竞争。我们发现MvfR抑制改变了竞争性种间相互作用,并保留了铜绿假单胞菌与ESKAPEE病原体的共存,同时解除了病原体形成生物膜和粘附在肺上皮细胞上的能力。我们的研究结果强调了MvfR抑制在调节多物种微生物竞争相互作用中的作用,同时减弱了毒力性状。这些发现揭示了QS在种间相互作用中的复杂性和重要性,并强调了抗毒力方法在微生物生态学中的影响及其在治疗多微生物感染中的重要性。
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来源期刊
Cells
Cells Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
9.90
自引率
5.00%
发文量
3472
审稿时长
16 days
期刊介绍: Cells (ISSN 2073-4409) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to cell biology, molecular biology and biophysics. It publishes reviews, research articles, communications and technical notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided.
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