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喹诺酮类耐药机制:靶点改变、蓄积减少及DNA回旋酶保护。

Mechanisms of resistance to quinolones: target alterations, decreased accumulation and DNA gyrase protection.

作者信息

Ruiz Joaquim

机构信息

Department of Microbiology, Institut Clínic Infeccions i Immunologia, Hospital Clínic, C/.Villarroel 170, 08036-Barcelona, Spain.

出版信息

J Antimicrob Chemother. 2003 May;51(5):1109-17. doi: 10.1093/jac/dkg222. Epub 2003 Apr 14.

Abstract

Quinolones are broad-spectrum antibacterial agents, commonly used in both clinical and veterinary medicine. Their extensive use has resulted in bacteria rapidly developing resistance to these agents. Two mechanisms of quinolone resistance have been established to date: alterations in the targets of quinolones, and decreased accumulation due to impermeability of the membrane and/or an overexpression of efflux pump systems. Recently, mobile elements have also been described, carrying the qnr gene, which confers resistance to quinolones.

摘要

喹诺酮类是广谱抗菌剂,常用于临床医学和兽医学。它们的广泛使用已导致细菌迅速对这些药物产生耐药性。迄今为止,已确定了两种喹诺酮耐药机制:喹诺酮类药物靶点的改变,以及由于细胞膜通透性降低和/或外排泵系统过表达导致的药物蓄积减少。最近,还发现了携带qnr基因的可移动元件,该基因赋予对喹诺酮类药物的耐药性。

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