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铜绿假单胞菌临床和环境分离株对氟喹诺酮类药物耐药性的诱导

Induction of resistance to fluoroquinolones in clinical and environmental isolates of Pseudomonas aeruginosa.

作者信息

Prasad S Vishnu, Ballal Mamatha, Shivananda P G

机构信息

Department of Microbiology, Kasturba Medical College, Manipal and Sikkim Institute of Medical Sciences, Gangtok, Sikkim.

出版信息

Indian J Pathol Microbiol. 2007 Jan;50(1):94-6.

Abstract

An attempt to induce resistance to ciprofloxacin in vitro was made against clinical and environmental isolates of Pseudomonas aeruginosa. This in vitro manipulation of strains resulted in the increase of minimum inhibitory concentration from 0.4 microg/ml to 1 microg/ml of the original strains to 9.0 to 12.5 microg/ml indicating development of resistance to ciprofloxacin and a major decrease in the size of zone diameters of norfloxacin and ofloxacin indicating cross resistance to these agents. Results indicate the induced resistance to ciprofloxacin can promote development of cross resistance to other fluoroquinolones. This suggests that caution should be taken while using fluoroquinolones for the treatment of Pseudomonas aeruginosa infections.

摘要

针对铜绿假单胞菌的临床分离株和环境分离株进行了体外诱导对环丙沙星耐药性的尝试。对菌株的这种体外操作导致最低抑菌浓度从原始菌株的0.4微克/毫升增加到1微克/毫升,再到9.0至12.5微克/毫升,表明对环丙沙星产生了耐药性,并且诺氟沙星和氧氟沙星的抑菌圈直径大幅减小,表明对这些药物产生了交叉耐药性。结果表明,诱导产生的对环丙沙星的耐药性可促进对其他氟喹诺酮类药物交叉耐药性的产生。这表明在使用氟喹诺酮类药物治疗铜绿假单胞菌感染时应谨慎。

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