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In Vitro Activity of Imipenem and Colistin against a Carbapenem-Resistant Klebsiella pneumoniae Isolate Coproducing SHV-31 CMY-2 and DHA-1

机译:亚胺培南和colistin的抗碳青霉烯耐药肺炎克雷伯菌肺炎克雷伯菌分离株共同生产SHV-31CMY-2和DHA-1的体外活性。

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摘要

We investigated the synergism of colistin and imipenem against a multidrug-resistant K. pneumoniae isolate 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 common β-lactamases and carbapenemases. Synergism was evaluated by time-kill studies. The bla SHV-31, bla CMY-2, and bla DHA-1 were detected. Outer membrane porin genes analysis revealed loss of ompK36 and frame-shift mutation of ompK35. 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-resistant K. pneumoniae infections.
机译:我们调查了大肠菌素和亚胺培南对多药耐药的肺炎克雷伯菌分离株的协同作用,该分离株从严重的髋部感染中恢复。 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bla SHV-31,bla CMY-2和bla DHA-1。外膜孔蛋白基因分析显示ompK36的丢失和ompK35的移码突变。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(2μmg/ L)和亚胺培南1x MIC(8μmg/ L)的组合具有协同作用和杀菌作用,但具有接种作用。通过单独添加粘菌素2x MIC或加亚胺培南2x MIC观察到无接种效果的杀菌活性。总之,粘菌素加亚胺培南可能是治疗耐碳青霉烯的肺炎克雷伯菌感染的替代选择。

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