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重症监护病区碳青霉烯类耐药肠杆菌科细菌的主动筛查及基因分析

The active screening carbapenem-resistant Enterobacteriaceae in intensive care unit and gene analysis

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目的 调查重症监护病区(ICU)患者在住院期间碳青霉烯类耐药肠杆菌科细菌(CRE)主动筛查菌株的分布以及CRE耐药基因的检测和分析.方法 收集424例ICU患者直肠拭子、咽拭子和腹股沟拭子样本,采用肉汤增菌法进行CRE阳性病例的主动筛查,全自动药敏分析仪进行体外药敏试验,PCR法检测碳青霉烯酶耐药基因,通过多位点序列分型(MLST)和肠杆菌基因间重复共有序列PCR分析CRE菌株的同源性关系.结果 直肠拭子、咽拭子和腹股沟拭子CRE筛查阳性率分别为12.5%、5.0%和4.2%,CRE菌株主要来自肺炎克雷伯菌(82.6%)、大肠埃希菌(9.8%)和产气肠杆菌(4.3%),CRE菌株对替加环素、头孢他啶阿维巴坦敏感性较好(>90%);92株CRE碳青霉类耐药基因检测,以blaKPC-2亚型(91.3%)为主;MLST分型结果显示76株碳青霉烯类耐药肺炎克雷伯菌(CRKP)主要为ST11型(69.7%)和ST15型(28.9%);ERIC-PCR扩增结果分析显示,76株肺炎克雷伯菌主要为谱型A(69.7%)和谱型B(28.9%).结论 ICU住院患者CRE主动筛查以blaKPC-2亚型的CRKP为主,MLST分型和ERIC-PCR扩增结果聚类分析发现主要存在两个克隆株传播.
Objective To investigate the distribution of carbapenem-resistant Enterobacteriaceae(CRE)in intensive care unit(ICU)during hospitalization,examine and analyze CRE-related genes.Methods Rectal swabs,throat swabs,and groin swabs were collected.Broth cultivation was used amplify the samples from above swabs and screen CRE positive cases.Automatic drug sensitivity analyzer was used for in vitro drug sensitivity testing.PCR was applied to detect CRE genes.Multi-locus sequence typing(MLST)and Enterobacterial repetitive intergenic consensus(ERIC)PCR were used to determine homologous relationship.Results The positive rates of CRE in rectal swabs,throat swabs,and groin swabs were 12.5%,5.0%,and 4.2%respectively.The main CRE strains were Klebsiella pneumoniae(82.6%),Escherichia coli(9.8%),and Enterobacter aerogenes(4.3%).CRE strains exhibited good sensitivity to tigecycline,cefotaxime,and avibactam(>90%).A total of 92 CRE strains were detected,and bla KPC-2 subtype was predominant,accounting for 91%.MLST typing results indicated that the majority of carbapenem-resistant K.pneumoniae(CRKP)belonged to ST11 type(69.7%),followed by ST15 type(28.9%).ERIC-PCR analysis demonstrated that most K.pneumoniae strains belonged to type A(69.7%)or type B(28.9%).Conclusion CRKP of bla KPC-2 subtype is a major strain found by active screening of CRE in ICU inpatients.MLST typing and cluster analysis of ERIC-PCR amplification reveal the spread of two clonal strains.

intensive care unitcarbapenem-resistant Enterobacteriaceaebacterium screeningdrug resistant gene testingmulti-locus sequence typingEnterobacterial repetitive intergenic consensus PCR

张慧、周聪、徐茂锁、余司文、申春梅、林勇

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复旦大学附属上海市第五人民医院检验科,上海 200240

复旦大学附属上海市第五人民医院院感科,上海 200240

重症监护病区 碳青霉烯类耐药肠杆菌科 细菌筛查 耐药基因检测 多位点序列分型 肠杆菌基因间重复共有序列PCR

2024

贵州医科大学学报
贵阳医学院

贵州医科大学学报

CSTPCD
影响因子:0.827
ISSN:2096-8388
年,卷(期):2024.49(11)