Multidrug-resistant bacteria quorum-sensing inhibitors: A particular focus on Pseudomonas aeruginosa

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2024-10-29 DOI:10.1016/j.ejmech.2024.117008
Aichata Maiga , Maxwell Ampomah-Wireko , Hongteng Li , Zhengmin Fan , Ziwei Lin , Haojie Zhen , Stephen Kpekura , Chunli Wu
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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.

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耐多药细菌法定人数感应抑制剂:特别关注铜绿假单胞菌。
由于铜绿假单胞菌(P. aeruginosa)对大多数临床相关抗菌药物的耐药性不断增强,许多广泛使用的常规抗生素都未能显示出对铜绿假单胞菌的临床疗效。铜绿假单胞菌利用法定人数感应来调节其毒力和生物膜的发展,这导致了其致病性和耐药性。这种机制是感染复发和持续存在的原因。因此,通过法定量感应(QS)来针对铜绿假单胞菌的毒力和致病性被认为是抗感染治疗的潜在靶点。然而,许多天然和合成化合物已被证明能干扰法定人数感应,从而产生潜在的抗菌剂。在这篇综述中,我们将讨论铜绿假单胞菌法定人数感应的机制,以及最近在开发有可能成为有效抗生素的法定人数感应抑制剂(包括合成的和天然的)方面取得的进展。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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