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首页> 外文期刊>Journal of microbiology, immunology, and infection: Wei mian yu gan ran za zhi >Nationwide spread of Klebsiella pneumoniae carbapenemase-2-producing K. pneumoniae sequence type 11 in Taiwan
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Nationwide spread of Klebsiella pneumoniae carbapenemase-2-producing K. pneumoniae sequence type 11 in Taiwan

机译:台湾产肺炎克雷伯菌肺炎克雷伯菌酶2的肺炎克雷伯菌序列11型在全国范围内传播

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摘要

Since the past decade, carbapenem-resistant Enter-obacteriaceae isolates, particularly Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae and New Delhi metallo-p-lactamase-1 (NDM-1)-producing Enter-obacteriaceae, have emerged in health care settings of many countries. Apart from NDM, which is endemic in the Indian subcontinent, KPC was first reported among K. pneumoniae in the United States in 2001 and has also been proven to possess great potential for intra- and interhospital dissemination worldwide. The first clinical KPC-producing K. pneumoniae isolate in Taiwan was obtained in 2010 from a patient with bacteremia who had just returned from Zhejiang Province, the epicenter of the KPC-2 endemic in China.4 For most clinical laboratories, however, it is difficult to judge the existence of carbape-nemases in Enterobacteriaceae through minimum inhibitory concentration (MIC) levels against carbapenem agents alone. In 2009, by means of the modified Hodge test, no ertapenem-nonsusceptible (NS; MIC > 0.25 (mug/mL) Enterobacteriaceae isolates of class A carbapenemase production were detected in intensive care units in Taiwan. However, using the MIC breakpoints recommended by the Clinical and Laboratory Standards Institute (CLSI) in 2011, we found alarmingly high rates of nonsusceptibility of Enterobacter cloacae and K. pneumoniae to ertapenem (40.5% and 24.5%, respectively). Subsequently, using the polymerase chain reaction method and electrophoresis analysis, two nationwide surveys in Taiwan investigated the 2011 prevalence rates of Enterobacteriaceae carriers of carbapenemases (class A, class B) and elucidated the main resistance mechanisms of carbapenem-NS Enterobacteriaceae isolates collected in 2010 and 2012, respectively.
机译:自过去的十年以来,抗碳青霉菌的肠杆菌科细菌,尤其是产生肺炎克雷伯菌的碳青霉烯酶(KPC)和生产新德里金属对β-内酰胺酶-1(NDM-1)的肠杆菌科细菌在健康中已经出现。许多国家的医疗机构。除了在印度次大陆流行的NDM以外,KPC于2001年在美国的肺炎克雷伯菌中首次被报道,并且已被证明具有在全世界医院内和医院间传播的巨大潜力。台湾首例临床生产KPC的肺炎克雷伯菌分离株是2010年从一名刚从浙江省返回的细菌血症患者那里获得的,而浙江省是中国KPC-2地方性流行的中心。4然而,对于大多数临床实验室而言,难以通过仅对碳青霉烯类药物的最低抑菌浓度(MIC)水平来判断肠杆菌科中是否存在碳青霉病。 2009年,通过改良的Hodge检验,在台湾的重症监护病房中未检测到厄他培南不敏感(NS; MIC> 0.25(Mug / mL)A类碳青霉烯酶产肠杆菌科细菌的分离株,但是使用了在2011年临床和实验室标准协会(CLSI)中,我们发现阴沟肠杆菌和肺炎克雷伯菌对ertapenem的不敏感率很高(分别为40.5%和24.5%),随后使用聚合酶链反应法和电泳分析,台湾的两项全国性调查均调查了2011年碳青霉烯酶的肠杆菌科细菌携带者(A类,B类)的患病率,并阐明了分别于2010年和2012年收集到的碳青霉烯-NS肠杆菌科细菌的主要耐药机制。

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