细菌外膜囊泡增加了铜绿假单胞菌对多粘菌素的抗性,同时抑制了其法定人数感应。

Journal of hazardous materials Pub Date : 2024-10-05 Epub Date: 2024-08-22 DOI:10.1016/j.jhazmat.2024.135588
Zhihui Chen, Yucheng Liu, Lan Jiang, Chao Zhang, Xun Qian, Jie Gu, Zilin Song
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引用次数: 0

摘要

耐多药细菌病原体的持续出现导致抗生素的疗效下降,其中铜绿假单胞菌(P. aeruginosa)是一个显著的威胁。我们对铜绿假单胞菌的抗生素耐药性和法定量感应(QS)系统进行了研究,重点是作为抗生素最后一道防线的外膜囊泡和多粘菌素 B。我们的研究结果表明,外膜囊泡增加了铜绿微囊藻对多粘菌素 B 的抗药性。铜绿微囊藻体内的整体基因转录水平也表明,外膜囊泡能降低多粘菌素 B 的药效,但外膜囊泡和亚致死浓度的多粘菌素 B 都抑制了与 QS 系统相关的基因转录水平。此外,OMVs 和多粘菌素 B 对铜绿微囊藻的 QS 系统协同作用,产生了更强的抑制效果。这种抑制作用表现为毒力因子分泌减少、细菌运动能力受损以及形成生物膜的能力明显下降。这些结果表明,OMVs 增强了铜绿假单胞菌对多粘菌素 B 的耐药性,但它们与多粘菌素 B 共同抑制了 QS 系统。我们的研究有助于更深入地了解环境中铜绿假单胞菌的抗性机制,并为通过 QS 系统减少铜绿假单胞菌引起的细菌感染提供了新的见解。
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Bacterial outer membrane vesicles increase polymyxin resistance in Pseudomonas aeruginosa while inhibiting its quorum sensing.

The persistent emergence of multidrug-resistant bacterial pathogens is leading to a decline in the therapeutic efficacy of antibiotics, with Pseudomonas aeruginosa (P. aeruginosa) emerging as a notable threat. We investigated the antibiotic resistance and quorum sensing (QS) system of P. aeruginosa, with a particular focused on outer membrane vesicles (OMVs) and polymyxin B as the last line of antibiotic defense. Our findings indicate that OMVs increase the resistance of P. aeruginosa to polymyxin B. The overall gene transcription levels within P. aeruginosa also reveal that OMVs can reduce the efficacy of polymyxin B. However, both OMVs and sublethal concentrations of polymyxin B suppressed the transcription levels of genes associated with the QS system. Furthermore, OMVs and polymyxin B acted in concert on the QS system of P. aeruginosa to produce a more potent inhibitory effect. This suppression was evidenced by a decrease in the secretion of virulence factors, impaired bacterial motility, and a notable decline in the ability to form biofilms. These results reveal that OMVs enhance the resistance of P. aeruginosa to polymyxin B, yet they collaborate with polymyxin B to inhibit the QS system. Our research contribute to a deeper understanding of the resistance mechanisms of P. aeruginosa in the environment, and provide new insights into the reduction of bacterial infections caused by P. aeruginosa through the QS system.

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