Multidrug resistance in Pseudomonas aeruginosa: genetic control mechanisms and therapeutic advances.

IF 6.3 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yuanjing Zhao, Haoran Xu, Hui Wang, Ping Wang, Simin Chen
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Abstract

Pseudomonas aeruginosa is a significant opportunistic pathogen, and its complex mechanisms of antibiotic resistance pose a challenge to modern medicine. This literature review explores the advancements made from 1979 to 2024 in understanding the regulatory networks of antibiotic resistance genes in Pseudomonas aeruginosa, with a particular focus on the molecular underpinnings of these resistance mechanisms. The review highlights four main pathways involved in drug resistance: reducing outer membrane permeability, enhancing active efflux systems, producing antibiotic-inactivating enzymes, and forming biofilms. These pathways are intricately regulated by a combination of genetic regulation, transcriptional regulators, two-component signal transduction, DNA methylation, and small RNA molecules. Through an in-depth analysis and synthesis of existing literature, we identify key regulatory elements mexT, ampR, and argR as potential targets for novel antimicrobial strategies. A profound understanding of the core control nodes of drug resistance offers a new perspective for therapeutic intervention, suggesting that modulating these elements could potentially reverse resistance and restore bacterial susceptibility to antibiotics. The review looks forward to future research directions, proposing the use of gene editing and systems biology to further understand resistance mechanisms and to develop effective antimicrobial strategies against Pseudomonas aeruginosa. This review is expected to provide innovative solutions to the problem of drug resistance in infectious diseases.

铜绿假单胞菌的多药耐药性:基因控制机制和治疗进展。
铜绿假单胞菌是一种重要的机会性病原体,其复杂的抗生素耐药性机制给现代医学带来了挑战。这篇文献综述探讨了从 1979 年到 2024 年在了解铜绿假单胞菌抗生素耐药基因调控网络方面取得的进展,尤其侧重于这些耐药机制的分子基础。综述重点介绍了涉及耐药性的四种主要途径:降低外膜渗透性、增强活性外排系统、产生抗生素失活酶和形成生物膜。这些途径受到基因调控、转录调控因子、双组分信号转导、DNA 甲基化和小 RNA 分子的综合调控,错综复杂。通过对现有文献的深入分析和综合,我们确定了关键调控元件 mexT、ampR 和 argR,并将其作为新型抗菌策略的潜在靶标。对耐药性核心控制节点的深刻理解为治疗干预提供了新的视角,表明调节这些元素有可能逆转耐药性,恢复细菌对抗生素的敏感性。综述展望了未来的研究方向,提出利用基因编辑和系统生物学进一步了解耐药性机制,并开发针对铜绿假单胞菌的有效抗菌策略。这篇综述有望为解决传染病的耐药性问题提供创新的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
0.00%
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0
审稿时长
10 weeks
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