2014年至2018年在突尼斯一家医院收集的耐厄他培烯肠杆菌科细菌中碳青霉烯酶的筛查

European Journal of Microbiology & Immunology Pub Date : 2019-02-13 eCollection Date: 2019-03-18 DOI:10.1556/1886.2018.00033
Hans Kollenda, Hagen Frickmann, Rania Ben Helal, Dorothea Franziska Wiemer, Habiba Naija, Mohamed Sélim El Asli, Melanie Egold, Joachim Jakob Bugert, Susann Handrick, Roman Wölfel, Farouk Barguellil, Mohamed Ben Moussa
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引用次数: 19

摘要

背景:从突尼斯患者分离的肠杆菌科细菌中经常检测到碳青霉烯耐药性。该研究旨在鉴定突尼斯分离株中常见的碳青霉烯酶。方法:2014年5月至2018年1月,在突尼斯军队医院微生物科分离到197株耐厄他培宁肠杆菌。对菌株进行了表型鉴定,然后进行了针对碳青霉烯酶基因blaIMP、blaVIM、blaNDM、blaSPM、blaAIM、blaDIM、blaGIM、blaSIM、blaKPC、blaBIC和blaOXA-48的内部聚合酶链反应(PCR)。结果:突尼斯197株耐埃他培宁肠杆菌科细菌包括肺炎克雷伯菌170株、阴沟肠杆菌19株、大肠杆菌6株、锡拉克柠檬酸杆菌1株、沙伯肠杆菌1株。因此,197个分离株中有55个(27.9%)来自血培养,表明是全身性疾病。碳青霉烯酶基因blaOXA-48数量最多,有153个检测,其次是blaNDM,有14个检测,分布在整个研究区间。相比之下,blaBIC和blaVIM仅分别在5例和3例中被罕见地发现,而其他碳青霉酰胺酶未被发现。结论:碳青霉烯酶基因blaOXA-48在绝大多数耐厄他培烯突尼斯肠杆菌科中被鉴定出来,而所有其他被评估的碳青霉烯酶的丰度都要低得多。在定量相关的少数分离株中,应用基于pcr的筛选方法未发现任何碳青霉烯酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening for Carbapenemases in Ertapenem-Resistant Enterobacteriaceae Collected at a Tunisian Hospital Between 2014 and 2018.

Background: Carbapenem-resistance is frequently detected in Enterobacteriaceae isolated from patients in Tunisia. The study was performed to identify frequent carbapenemases in Tunisian isolates.

Methods: Between May 2014 and January 2018, 197 ertapenem-resistant Enterobacteriaceae were isolated at the microbiological department of the Military Hospital of Tunis. The strains were phenotypically characterized and then subjected to in-house polymerase chain reaction (PCR) targeting the carbapenemase genes blaIMP, blaVIM, blaNDM, blaSPM, blaAIM, blaDIM,blaGIM, blaSIM, blaKPC, blaBIC , and blaOXA-48.

Results: The assessed 197 ertapenem-resistant Enterobacteriaceae from Tunis comprised 170 Klebsiella pneumoniae, 19 Enterobacter cloacae, 6 Escherichia coli, 1 Citrobacter sedlakii, and 1 Enterobacter asburiae. Thereby, 55 out of 197 isolates (27.9%) were from blood cultures, suggesting a systemic disease. The carbapenemase gene blaOXA-48 quantitatively dominated by far with 153 detections, followed by blaNDM with 14 detections, which were distributed about the whole study interval. In contrast, blaBIC and blaVIM were only infrequently identified in 5 and 3 cases, respectively, while the other carbapenamases were not observed.

Conclusions: The carbapenemase gene blaOXA-48 was identified in the vast majority of ertapenem-resistant Tunisian Enterobacteriaceae while all other assessed carbapenemases were much less abundant. In a quantitatively relevant minority of isolates, the applied PCR-based screening approach did not identify any carbapenemases.

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