Suppr超能文献

多药耐药菌群体感应抑制剂:特别关注铜绿假单胞菌。

Multidrug-resistant bacteria quorum-sensing inhibitors: A particular focus on Pseudomonasaeruginosa.

机构信息

School of Pharmaceutical Sciences, Key Laboratory of Advanced Pharmaceutical Technology, Ministry of Education of China, Zhengzhou University, Zhengzhou, 450001, PR China.

School of Nursing and Health, Ministry of Education of China, Zhengzhou University, Zhengzhou, 450001, PR China.

出版信息

Eur J Med Chem. 2025 Jan 5;281:117008. doi: 10.1016/j.ejmech.2024.117008. Epub 2024 Oct 29.

Abstract

Many widely used conventional antibiotics have failed to show clinical efficacy against Pseudomonas aeruginosa (P. aeruginosa) due to the strain's rising resistance to most clinically relevant antimicrobials. P. aeruginosa uses quorum sensing to regulate its virulence and biofilm development, which contributes to its pathogenicity and drug resistance. This mechanism is responsible for the resurgence and persistence of infections. Therefore, targeting the virulence and pathogenicity of P. aeruginosa through quorum sensing (QS) is regarded as a potential target for anti-infective therapy. However, a number of natural and synthetic compounds have been demonstrated to interfere with quorum sensing, resulting in potential antibacterial agents. In this review, we discuss the mechanisms of P. aeruginosa QS and recent advances in the development of quorum sensing inhibitors (both synthetic and natural) that have the potential to become effective antibiotics.

摘要

由于菌株对大多数临床相关抗菌药物的耐药性不断上升,许多广泛使用的传统抗生素在治疗铜绿假单胞菌(P. aeruginosa)方面均未显示出临床疗效。铜绿假单胞菌利用群体感应来调节其毒力和生物膜的形成,这有助于其致病性和耐药性。该机制是感染复发和持续存在的原因。因此,通过群体感应(QS)靶向铜绿假单胞菌的毒力和致病性被认为是一种有潜力的抗感染治疗靶点。然而,一些天然和合成化合物已被证明可以干扰群体感应,从而成为有潜力的抗菌药物。在这篇综述中,我们讨论了铜绿假单胞菌 QS 的机制以及群体感应抑制剂(天然和合成)的最新进展,这些抑制剂有可能成为有效的抗生素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验