Phenotypic Characterization of Extended-Spectrum Beta-Lactamases and Metallo-Beta-Lactamase of Multi Drug Resistant Acinetobacter baumannii Causing Nosocomial Infections in Erbil City

S. Smail, Kamal I. Al-Otrachi
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引用次数: 3

Abstract

Background: Resistance to broad‑spectrum beta‑lactams, mediated by extended‑spectrum beta‑lactamases, and metallo‑beta‑lactamase enzymes, is an increasing problem worldwide. The main aim is to study phenotypic characterization of extended‑spectrum beta‑lactamases and metallo‑beta‑lactamase multidrug resistant Acinetobacter baumannii in Erbil City. Materials and Methods: A total of 112 Acinetobacter baumannii isolations were collected from patients of all age groups from clinical specimens sputum, blood, pus, wound swab, urine and body fluids (Pleural fluid and cerebrospinal fluid) collected from different medical wards and intensive care unit departments of hospitals in Erbil City for a period of one year from march 2018--march 2019. Isolates were tested for the presence of extended‑spectrum beta‑lactamases and metallo‑beta‑lactamase. Detection of extended‑spectrum beta‑lactamases was done by the combined disk diffusion method according to Clinical and Laboratory Standards Institute guidelines, while metallo‑beta‑lactamase was detected by meropenem and imipenem combined with ethylenediaminetetraacetic acid disk method. Results: 25% (28) Acinetobacter baumannii isolates were positive for extended‑spectrum beta‑lactamases, while 100 % (112) were metallo‑beta‑lactamase producers. Conclusion: Acinetobacter baumannii is becoming a global medical challenge due to the emergence of multi-drug resistance. Newer beta lactamase is a matter of concern as they are developing rapidly and lead to treatment failure. Carbapenems are known to be effective therapeutic agents for Acinetobacter baumannii infections and its resistance limits the use to polymyxins and colistin. Several new medicines are still in research and combination of drug therapy is being currently used in the hospitals together with ours to treat multidrug resistant Acinetobacter baumannii infections.
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埃尔比勒市多重耐药鲍曼不动杆菌引起医院感染的广谱β -内酰胺酶和金属β -内酰胺酶表型特征
背景:由广谱β -内酰胺酶和金属β -内酰胺酶介导的广谱β -内酰胺耐药在世界范围内是一个日益严重的问题。主要目的是研究埃尔比勒市广谱β -内酰胺酶和金属β -内酰胺酶多重耐药鲍曼不动杆菌的表型特征。材料与方法:2018年3月- 2019年3月,从埃尔比勒市医院不同病房和重症监护病房收集临床标本,包括痰、血、脓、伤口拭子、尿液和体液(胸膜液和脑脊液),从各年龄组患者中分离出鲍曼不动杆菌112株。检测分离物是否存在广谱β -内酰胺酶和金属β -内酰胺酶。扩展谱β -内酰胺酶检测采用联合圆盘扩散法,按照临床与实验室标准协会指南,金属β -内酰胺酶检测采用美罗培南、亚胺培南联合乙二胺四乙酸圆盘法。结果:25%(28株)鲍曼不动杆菌对广谱β -内酰胺酶呈阳性,100%(112株)为金属β -内酰胺酶产生菌。结论:鲍曼不动杆菌因出现多重耐药而成为全球性的医学挑战。较新的β内酰胺酶是一个值得关注的问题,因为它们发展迅速,导致治疗失败。碳青霉烯类已知是鲍曼不动杆菌感染的有效治疗剂,其耐药性限制了多粘菌素和粘菌素的使用。一些新药仍在研究中,目前正在与我们的医院一起使用药物联合治疗来治疗多重耐药鲍曼不动杆菌感染。
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