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主动外排系统在沙门氏菌临床分离株喹诺酮耐药性中的重要性

The importance of active efflux systems in the quinolone resistance of clinical isolates of Salmonella spp.

作者信息

Escribano Isabel, Rodríguez Juan Carlos, Cebrian Laura, Royo Gloria

机构信息

Servicio de Microbiología, Hospital General Universitario de Elche, Camí de l'almazara s/n, 03203 Elche Alicante, Spain.

出版信息

Int J Antimicrob Agents. 2004 Nov;24(5):428-32. doi: 10.1016/j.ijantimicag.2004.05.004.

Abstract

The aim of this study was to determine the importance of the active elimination of antibiotics by active efflux systems, in the decrease in fluoroquinolone sensitivity of clinical isolates of Salmonella spp. as well as the intrinsic antibiotic activity of certain active efflux system inhibitors. The effect of the active efflux system on the decrease in sensitivity to nalidixic acid, ciprofloxacin, ofloxacin and sparfloxacin was studied by investigating the variation in the in vitro activity of these compounds when assayed in association with reserpine and MC 207.110. The active efflux systems inhibited by reserpine displayed low activity in the elimination of these compounds, whereas those inhibited by MC 207.110 showed high activity in the elimination of nalidixic acid and sparfloxacin, but were less effective in the elimination of ofloxacin and ciprofloxacin. These two compounds did not exhibit intrinsic inhibitory activity against Salmonella spp. at the concentrations assayed. These mechanisms of resistance to antibiotics are complex and vary depending on the chemical composition of the antibiotics used, and perhaps the inhibitors of these systems, although they do not exhibit any intrinsic antibiotic activity, may be used as adjuvants to increase the activity of certain antibiotics. These mechanisms complement the mutations in the gyrA gene and this supports the thesis that it is necessary to lower the breakpoint established by the NCCLS for ciprofloxacin, since the strains studied have resistance mechanisms that reduce the activity of this drug and may favour the emergence of resistant mutants during treatment.

摘要

本研究的目的是确定主动外排系统主动消除抗生素在沙门氏菌临床分离株对氟喹诺酮敏感性降低中的重要性,以及某些主动外排系统抑制剂的内在抗生素活性。通过研究这些化合物与利血平和MC 207.110联合检测时体外活性的变化,研究了主动外排系统对萘啶酸、环丙沙星、氧氟沙星和司帕沙星敏感性降低的影响。利血平抑制的主动外排系统在消除这些化合物方面活性较低,而MC 207.110抑制的主动外排系统在消除萘啶酸和司帕沙星方面活性较高,但在消除氧氟沙星和环丙沙星方面效果较差。这两种化合物在所检测的浓度下对沙门氏菌没有内在抑制活性。这些抗生素耐药机制很复杂,取决于所用抗生素的化学成分,也许这些系统的抑制剂虽然没有任何内在抗生素活性,但可作为佐剂来增强某些抗生素的活性。这些机制补充了gyrA基因突变,这支持了有必要降低NCCLS制定的环丙沙星断点的观点,因为所研究的菌株具有降低该药物活性的耐药机制,可能有利于治疗期间耐药突变体的出现。

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