Chauhan Kalpana, Pandey Anita, Asthana Ashish K, Madan Molly
Department of Microbiology, Subharti Medical College, Swami Vivekanand Subharti University, Meerut, Uttar Pradesh, India.
Indian J Pathol Microbiol. 2015 Jan-Mar;58(1):31-5. doi: 10.4103/0377-4929.151168.
Carbapenemase production is an important mechanism responsible for carbapenem resistance.
Phenotypic detection and differentiation of types of carbapenemase in carbapenem resistant Enterobacteriaceae is important for proper infection control and appropriate patient management.
We planned a study to determine the occurrence of Class A Klebsiella pneumoniae carbapenemase (KPC type) and Class B Metallo-β-lactamase (MBL type) carbapenemase in hospital and community.
Clinical isolates of Escherichia coli and Klebsiella species and simultaneously evaluate different phenotypic methods for detection of carbapenemases.
It was observed that 20.72% clinical isolates of E. coli and Klebsiella spp. were resistant to carbapenem on screening of which, 14.64% were E. coli and 29.69% were Klebsiella spp. Using phenotypic confirmatory tests the occurrence of carbapenemase production was found to be 87.01% in E. coli and 91.51% in Klebsiella spp. using both modified Hodge test (MHT) and combined disk test (CDT) using imipenem-ethylenediaminetetraacetic acid.
Both MBL and KPC type carbapenemases were seen among clinical isolates of E. coli and Klebsiella spp. CDT is simple, rapid and technically less demanding procedure, which can be used in all clinical laboratories. Supplementing MHT with CDT is reliable phenotypic tests to identify the class A and class B carbapenemase producers.
碳青霉烯酶的产生是导致碳青霉烯耐药的重要机制。
对耐碳青霉烯肠杆菌科细菌中的碳青霉烯酶类型进行表型检测和区分,对于正确的感染控制和恰当的患者管理至关重要。
我们计划开展一项研究,以确定医院和社区中A类肺炎克雷伯菌碳青霉烯酶(KPC型)和B类金属β-内酰胺酶(MBL型)碳青霉烯酶的发生率。
收集大肠杆菌和克雷伯菌属的临床分离株,并同时评估检测碳青霉烯酶的不同表型方法。
在筛选的大肠杆菌和克雷伯菌属临床分离株中,观察到20.72%对碳青霉烯耐药,其中14.64%为大肠杆菌,29.69%为克雷伯菌属。使用表型确证试验,发现使用亚胺培南-乙二胺四乙酸的改良 Hodge试验(MHT)和联合纸片试验(CDT)时,大肠杆菌中碳青霉烯酶产生率为87.01%,克雷伯菌属中为91.51%。
在大肠杆菌和克雷伯菌属的临床分离株中均发现了MBL型和KPC型碳青霉烯酶。CDT是一种简单、快速且技术要求较低的方法,可用于所有临床实验室。用CDT补充MHT是鉴定A类和B类碳青霉烯酶产生菌的可靠表型试验。