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MAST D73C组合纸片法检测肠杆菌科细菌碳青霉烯酶
引用本文:田东兴,张泓.MAST D73C组合纸片法检测肠杆菌科细菌碳青霉烯酶[J].中国抗感染化疗杂志,2020(1):81-85.
作者姓名:田东兴  张泓
作者单位:上海交通大学附属儿童医院
基金项目:上海市卫计委重要薄弱学科建设(2015ZB0203);第四轮公共卫生三年行动计划重点学科项目(15GWZK0101)。
摘    要:目的使用MAST D73C组合纸片法检测儿童碳青霉烯类耐药肠杆菌科细菌(CRE)菌株中碳青霉烯酶及其分型,为临床提供一种简便快速的碳青霉烯酶检测方法。方法MAST D73C组合纸片法和PCR基因检测确认240株儿童临床分离CRE菌株碳青霉烯酶基因,并用统计学方法分析MAST D73C检测碳青霉烯酶的灵敏度和特异度。结果233株CRE碳青霉烯酶基因表达阳性,blaNDM、blaOXA-232、blaKPC-2和blaIMP检出率分别为40.00%、28.75%、23.33%和4.17%,另有2株同时携带2种碳青霉烯酶基因。MAST D73C组合纸片对MβL酶、OXA-48酶和KPC酶的检出率分别为48.48%(112/231)、27.27%(63/231)和8.66%(20/231),另有36株(15.58%)细菌抑菌圈结果无法解释。与PCR方法相比,MAST D73C检测MβL酶的灵敏度和特异度分别为99.06%和94.40%;检测OXA-48酶的灵敏度和特异度为81.16%和95.68%;检测KPC酶的灵敏度和特异度为33.93%和99.43%,但采用法罗培南耐药判断该菌为产KPC型碳青霉烯酶的补充标准后,灵敏度提高至87.50%,并且检测其他酶型的灵敏度和特异度不变,与PCR结果相比总符合率为90.91%(210/231)。结论儿童分离CRE菌株主要检出NDM-1酶和OXA-232酶,MAST D73C组合纸片法补充解释标准后可以简便、快速、准确地检测碳青霉烯酶,并可将其分型。

关 键 词:肠杆菌科细菌  碳青霉烯酶  检测方法  儿童

MASTDISCS combi Carba plus disc system D73C,a method for identifying carbapenemase phenotypes among Enterobacteriaceae
TIAN Dongxing,ZHANG Hong.MASTDISCS combi Carba plus disc system D73C,a method for identifying carbapenemase phenotypes among Enterobacteriaceae[J].Chinese Journal of Infection and Chemotherapy,2020(1):81-85.
Authors:TIAN Dongxing  ZHANG Hong
Affiliation:(Department of Laboratory Medicine,Shanghai Children's Hospital,Shanghai Jiao Tong University,Shanghai 200040,China)
Abstract:Objective To describe a simple and accurate method,MASTDISCS■combi Carba plus disc system D73C,for identifying carbapenemase phenotypes in the carbapenem-resistant Enterobacteriaceae(CRE)strains isolated from children.Methods MASTDISCS■D73C and polymerase chain reaction(PCR)were used for analysis of carbapenemase phenotypes and genotypes in 240 non-duplicate carbapenem-resistant Enterobacteriaceae strains.The sensitivity and specificity of MASTDISCS■D73C in detection of carbapenemases were evaluated by statsitical analysis.Results Carbapenemases were expressed in 233 strains.The prevalence of blaNDM,blaOXA-232,blaKPC-2,and blaIMP was 40.00%,28.75%,23.33%,and 4.17%,respectively.Two strains were positive simultaneously for 2 carbapenemase genes.Metallo-β-lactamase,OXA-48,and KPC carbapenemases were identified by MASTDISCS■D73C in 48.48%,27.27%,and 8.66%of the strains.Equivocal result was generated in 36(15.58%)strains.The sensitivity and specificity of MASTDISCS■D73C were 99.06%and 94.40%in identifying metallo-β-lactamase;81.16%and 95.68%in detecting OXA-48 carbapenemase;33.93%and 99.43%in identifying KPC carbapenemase.When KPCproducers were counted according to faropenem breakpoints,the sensitivity of MASTDISCS■D73C increased to 87.50%in detection of KPC carbapenemase,but its sensitivity and specificity remained stable for other carbapenemases.Conclusions NDM-1 and OXA-232 were the most prevalent carbapenemases in the CRE strains isolated from children.MASTDISCS■combi Carba plus disc system D73C is a simple,quick,and accurate method for discriminating the types of carbapenemase produced by CRE strains when faropenem breakpoints are considered to judge KPC-producers.
Keywords:Enterobacteriaceae  carbapenemase  testing method  children
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