Department of Microbiology, Medical School, University of Thessaly, Larissa, Greece.
J Clin Microbiol. 2010 Jul;48(7):2601-4. doi: 10.1128/JCM.02134-09. Epub 2010 May 26.
Meropenem heteroresistance was investigated in six apparently meropenem-susceptible, Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae (KPC-KP) clinical isolates, compared with that in carbapenemase-negative, meropenem-susceptible controls. In population analyses, the KPC-KP isolates grew at meropenem concentrations of 64 to 256 microg/ml. Heteroresistant colonies had significantly elevated expression of the bla(KPC) gene compared with the native populations but did not retain heteroresistance when subcultured in drug-free media. Time-kill assays indicated that meropenem alone was not bactericidal against KPC-KP but efficiently killed the control strains.
研究了 6 株产碳青霉烯酶肺炎克雷伯菌(KPC-KP)的临床分离株,这些分离株在表型上对美罗培南敏感,但实际上存在美罗培南异质性耐药,与碳青霉烯酶阴性、美罗培南敏感的对照株进行了比较。在群体分析中,KPC-KP 分离株在美罗培南浓度为 64 至 256μg/ml 时生长。与原始种群相比,异质性耐药菌的 bla(KPC)基因表达水平显著升高,但在无药物培养基中传代培养时,异质性耐药性消失。时间杀伤试验表明,美罗培南单独使用对 KPC-KP 没有杀菌作用,但能有效杀死对照株。