首页> 外文期刊>Iranian Journal of Microbiology >Isolation and genetic characterization of metallo-β-lactamase and carbapenamase producing strains of Acinetobacter baumannii from patients at Tehran hospitals
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Isolation and genetic characterization of metallo-β-lactamase and carbapenamase producing strains of Acinetobacter baumannii from patients at Tehran hospitals

机译:德黑兰医院患者鲍曼不动杆菌产金属β-内酰胺酶和碳青霉烯酶的菌株的分离和遗传特性

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Background and Objective: Carbapenems are therapeutic choice against infections caused by gram-negative bacilli including strains of Acinetobacter baumannii. Resistance to these antibiotics is mediated by efflux pumps, porins, PBPs and ?-lactamases. The aim of this study was to determine the possibility of existence of MBLs, OXAs and GES-1 betalactamase genes among clinical isolates of Acinetobacter collected from Tehran hospitals.Material and Methods: Two hundred and three Acinetobacter isolates were collected from patient at Tehran hospitals. The isolates were identified using biochemical tests. The susceptibility to different antibiotics was evaluated by disk diffusion method and MICs of imipenem were determined using Micro broth dilution method (CLSI). PCR was performed for detection of blaVIM-2, blaSPM-1, blaIMP-2, blaGES-1, blaOXA-51, blaOXA-23 betalactamase genes. Clonal relatedness was estimated by PFGE with the restriction enzyme SmaI.Results and Conclusion: Of 100 isolates of imipenem resistant Acinetobacter spp. collected from Tehran hospitals in 2009 and 2010, 6 isolates produced metallo-beta-lactamases and 94 isolates produced OXA- type carbapenemase. The blaSPM-1, blaGES-1, blaOXA-51, blaOXA-23 genes were detected by PCR among 6, 2, 94 and 84 isolates of A. baumannii, respectively. The MICs of isolates to imipenem were 8-128 μg/mL. PFGE analysis of 29 blaOXA-51 and blaOXA-23-positive A. baumannii isolates gave 6 different patterns. This is the first report of SPM-1 and GES-1 beta-lactamase producing A. baumannii. Production of the OXA-23, OXA-51, GES-1 and SPM-1 enzyme presents an emerging threat of carbapenem resistance among A. baumannii in Iran.
机译:背景与目的:碳青霉烯类是治疗革兰氏阴性杆菌(包括鲍曼不动杆菌)引起的感染的治疗选择。对这些抗生素的抗性由外排泵,孔蛋白,PBP和β-内酰胺酶介导。这项研究的目的是确定从德黑兰医院收集的临床不动杆菌中存在MBLs,OXAs和GES-1β-内酰胺酶基因的可能性。材料与方法:从德黑兰医院的患者中收集了203株不动杆菌。使用生化测试鉴定了分离物。通过圆盘扩散法评估对不同抗生素的敏感性,并使用微肉汤稀释法(CLSI)测定亚胺培南的MIC。进行PCR以检测blaVIM-2,blaSPM-1,blaIMP-2,blaGES-1,blaOXA-51,blaOXA-23β-内酰胺酶基因。通过PFGE和限制性内切酶SmaI进行克隆相关性评估。结果与结论:在100株亚胺培南耐药的不动杆菌属菌株中。在2009年和2010年从德黑兰医院收集的样本中,有6种分离物产生了金属β-内酰胺酶,有94种分离物产生了OXA型碳青霉烯酶。通过PCR分别在鲍曼不动杆菌的6、2、94和84个分离株中检测到blaSPM-1,blaGES-1,blaOXA-51,blaOXA-23基因。亚胺培南分离物的MIC值为8-128μg/ mL。对29种blaOXA-51和blaOXA-23阳性鲍曼不动杆菌的PFGE分析给出了6种不同的模式。这是SPM-1和GES-1β-内酰胺酶生产鲍曼不动杆菌的首次报道。在伊朗鲍曼不动杆菌中,OXA-23,OXA-51,GES-1和SPM-1酶的产生对碳青霉烯类药物产生了新的威胁。

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