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首页> 外文期刊>Infection and Drug Resistance >Molecular and phenotypical characterization of two cases of antibiotic-driven ceftazidime-avibactam resistance in bla KPC-3 -harboring Klebsiella pneumoniae
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Molecular and phenotypical characterization of two cases of antibiotic-driven ceftazidime-avibactam resistance in bla KPC-3 -harboring Klebsiella pneumoniae

机译:两例抗生素驱动的头孢他啶-avibactam耐药性感染bla KPC-3的肺炎克雷伯氏菌的分子和表型特征

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Background: For years, Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae have represented a serious health problem in hospitals worldwide. Since its approval in 2015, ceftazidime-avibactam (CAZ-AVI) had been successfully used for treating complicated KPC-K. pneumoniae infections, until increasing reports of resistance began to emerge. Methods: Phenotypic tests and molecular analysis were performed in four multidrug-resistant K. pneumoniae isolates, collected from two patients following treatment with CAZ-AVI. Results: In this study, we report two cases of emergence of CAZ-AVI resistance in KPC-3-producing K. pneumoniae isolates, collected from two patients following treatment with CAZ-AVI. Molecular analysis highlighted the D179Y mutation in the bla subKPC-3/sub gene, whose role in the loss of hydrolytic activity (resulting in decreased carpabenem minimum inhibitory concentrations and negative phenotypic tests) of the enzyme has already been shown. Conclusion: Most surveillance schemes aimed at detecting carbapenem-resistant Enterobacteriaceae (CRE) rely on confirmatory phenotypic tests for detecting carbapenemase production. As reports of these treatment-induced, altered CRE phenotypes are increasing, the initial susceptibility testing should be followed by a combination of phenotypic and molecular methods, to make sure that no potential carbapenemase-producing bacteria are missed.
机译:背景:多年来,肺炎克雷伯菌肺炎克雷伯菌(KPC)产生的肺炎克雷伯菌(K. pneumoniae)在世界各地的医院中代表着严重的健康问题。自2015年获批以来,头孢他啶-avibactam(CAZ-AVI)已成功用于治疗复杂的KPC-K。肺炎感染,直到越来越多的耐药性报告开始出现。方法:对四种抗药性肺炎克雷伯菌分离株进行了表型测试和分子分析,这些分离株是从两名接受CAZ-AVI治疗的患者中收集的。结果:在这项研究中,我们报道了从两名患者接受CAZ-AVI治疗后收集到的生产KPC-3的肺炎克雷伯菌中出现的2例CAZ-AVI抗药性病例。分子分析强调了bla KPC-3 基因中的D179Y突变,该突变在该酶的水解活性丧失(导致降低的羧苄青霉素最低抑菌浓度和阴性表型试验)中发挥了作用。结论:大多数旨在检测对碳青霉烯耐药的肠杆菌科(CRE)的监测方案都依赖于验证性表型测试来检测碳青霉烯酶的产生。随着这些治疗引起的CRE表型改变的报道不断增加,应在进行表型和分子方法相结合的初始药敏试验之后,确保不会遗漏任何潜在的产生碳青霉烯酶的细菌。

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