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首页> 外文期刊>BioMed research international >In Vitro Activity of Imipenem and Colistin against a Carbapenem-ResistantKlebsiella pneumoniaeIsolate Coproducing SHV-31, CMY-2, and DHA-1
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In Vitro Activity of Imipenem and Colistin against a Carbapenem-ResistantKlebsiella pneumoniaeIsolate Coproducing SHV-31, CMY-2, and DHA-1

机译:亚胺培南和共价素对耐碳青霉烯的肺炎克雷伯氏菌分离株共生产SHV-31,CMY-2和DHA-1的体外活性

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We investigated the synergism of colistin and imipenem against a multidrug-resistantK. pneumoniaeisolate which was recovered from a severe hip infection. PCR and DNA sequencing were used to characterize the outer membrane porin genes and the resistance genes mediating the commonβ-lactamases and carbapenemases. Synergism was evaluated by time-kill studies. TheblaSHV-31,blaCMY-2, andblaDHA-1were detected. Outer membrane porin genes analysis revealed loss ofompK36and frame-shift mutation ofompK35. The common carbapenemase genes were not found. Time-kill studies demonstrated that a combination of 1x MIC of colistin (2 mg/L) and 1x MIC of imipenem (8 mg/L) was synergistic and bactericidal but with inoculum effect. Bactericidal activity without inoculum effect was observed by concentration of 2x MIC of colistin alone or plus 2x MIC of imipenem. In conclusion, colistin plus imipenem could be an alternative option to treat carbapenem-resistantK. pneumoniaeinfections.
机译:我们调查了大肠粘菌素和亚胺培南对多药耐药K的协同作用。从严重的髋部感染中恢复出来的肺炎分离物。 PCR和DNA测序用于表征外膜孔蛋白基因和介导常见β-内酰胺酶和碳青霉烯酶的抗性基因。通过时间杀伤研究评估了协同作用。检测到blaSHV-31,blaCMY-2和blaDHA-1。外膜孔蛋白基因分析显示ompK36缺失和ompK35移码突变。找不到常见的碳青霉烯酶基因。时间杀灭研究表明,大肠菌素1x MIC(2 mg / L)和亚胺培南1x MIC(8 mg / L)的组合具有协同作用和杀菌作用,但具有接种作用。通过单独的粘菌素2x MIC浓度或加亚胺培南2x MIC浓度观察到没有接种效果的杀菌活性。总之,粘菌素加亚胺培南可能是治疗对碳青霉烯耐药的K的替代选择。肺炎感染。

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