中东三级保健中心对碳青霉烯类药物敏感性降低的肠杆菌科细菌的碳青霉烯酶分型和耐药性分析

Alexander Malek, Josselin Abi Chebl, H. Younes, J. Choucair, Nadim Azar
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摘要

目的:现在耐药细菌是世界范围内的一个公共卫生问题,在某些情况下导致僵局,没有任何可能的治疗。因此,早期检测和鉴定产碳青霉烯酶革兰氏阴性菌(GNB)至关重要。因此,我们在一家三级保健医院进行了一项研究,分析耐碳青霉烯类GNB (CRGNB)的耐药表型。方法:收集2014年9月至2016年1月收集的所有CRGNB菌株,随机抽取40/126株,采用敏感性试验和实时多重PCR检测准确的碳青霉烯酶编码基因(bla SPC、bla IMP1、bla VIM、bla NDM、bla KPC、bla OXA-48)。研究菌株为大肠埃希菌(70%)、肺炎克雷伯菌(20%)、产气肠杆菌(2.5%)、阴沟肠杆菌(2.5%)和产氧克雷伯菌(2.5%)。结果:100%的菌株对厄他培南中等或耐药,85%的菌株对亚胺培南和美罗培南中等或耐药。bla OXA-48阳性33 / 40株(82.5%),bla NDM阳性1株(2.5%)。OXA-48为尿路大肠杆菌菌株。6 / 40株(15%)未表达碳青霉烯酶基因。结论:我们注意到CPGNB的显著出现,特别是具有高耐药模式的bla OXA-48,导致治疗选择狭窄。这就需要迅速发现这种GNB菌株,以便迅速采取正确的预防和治疗措施,避免医院流行病造成灾难性后果。
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Carbapenemase typing and resistance profile of Enterobacteriaceae with reduced sensitivity to carbapenems in a Middle Eastern tertiary care center
Objective: nowadays resistant bacteria represent worldwide a public health problem leading in some cases to a stalemate without any possible treatment. Therefore early detection and identification of carbapenemase producing gram-negative bacteria (GNB) is of crucial importance. Consequently we conducted a study in a tertiary care hospital to analyze the resistance phenotype of the carbapenem resistant GNB (CRGNB). Methods: we collected all the CRGNB from September 2014 till January 2016, we took randomly 40/126 strains and performed a sensitivity test in addition to a real time multiplex PCR to detect the exact carbapenemase coding genes (bla SPC , bla IMP1, bla VIM , bla NDM , bla KPC , et bla OXA-48). The studied strains were: Escherichia coli (70%), Klebsiella pneumonia (20%), Enterobacter aerogenes (2,5%), Enterobacter cloacae (2.5%) et Klebsiella oxytoca (2.5%). Results: 100% of the studied strains were intermediate or resistant to ertapenem, 85% intermediate or resistant to imipenem and/or meropenem. 33 / 40 strains (82.5%) are bla OXA-48 positive et one strain (2.5%) is bla NDM positive. the OXA-48 were urinary strains of E coli. 6 / 40 strains (15%) did not express carbapenemase genes in molecular studies. Conclusion: we note a marked emergence of CPGNB especially bla OXA-48 with high resistance pattern leading to narrow therapeutic options. This requires a rapid detection of such strains of GNB so that to initiate quickly the right preventive and therapeutic measures to avoid hospital epidemics with disastrous consequences.
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