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Genotyping of ESBL Producing Uropathogenic Escherichia coli in West of Iran

机译:伊朗西部生产ESBL致病性大肠埃希菌的基因分型

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摘要

Background and Objective. Urinary tract infection (UTI) is one of the most common bacterial infections in the world. Molecular fingerprinting of UTI isolates such as pulsed-Field Gel Electrophoresis using for Clonal distribution and determine of predominant type. The aim of the study was to determine genotyping of ESBL producing UPECs. Material and Methods. 200 UPEC isolates from outpatients with UTI were obtained. Antimicrobial susceptibility and interpretation were performed by disk diffusion. Virulence factors for UPECs were screened by using PCR. UPECs were analyzed by Pulsed-Field Gel Electrophoresis and images analyzed by Phoretix1DPro software. Results. A total of 200 isolates of UPECs, 24.5% (n = 49) of isolates, were positive for ESBL production. Resistance ranged from 0% for amikacin and imipenem to over 93.9% for carbenicillin and ampicillin. Frequencies of haemagglutination, haemolysin, and hydrophobicity were 51%, 18.3%, and 14.28%, respectively. A total of 10 different genotypes were obtained, which include nine common clones and one single clone. Conclusion. We confirmed the prevalence of virulence phenotyping especially Haemagglutination among UPEC strains and that it can also contribute to virulence in these strains. Large diversity in genotypes was observed in the isolates that could be indicative of different sources of infection in community acquired.
机译:背景和目标。尿路感染(UTI)是世界上最常见的细菌感染之一。 UTI分离物的分子指纹图谱,例如用于克隆分布和确定主要类型的脉冲场凝胶电泳。该研究的目的是确定产生ESBL的UPEC的基因型。材料与方法。从门诊UTI患者中获得了200株UPEC分离株。抗菌药敏性和解释通过磁盘扩散进行。使用PCR筛选UPEC的毒力因子。 UPEC通过脉冲场凝胶电泳进行分析,图像通过Phoretix1DPro软件进行分析。结果。总共200株UPEC分离株,其中24.5%(n = 49)分离株对ESBL产生呈阳性。耐药性范围从阿米卡星和亚胺培南的0%到羧苄青霉素和氨苄青霉素的93.9%以上。血凝,溶血素和疏水性的频率分别为51%,18.3%和14.28%。总共获得了10种不同的基因型,包括9个常见克隆和1个单个克隆。结论。我们证实了UPEC菌株中毒力表型的普遍存在,尤其是血凝反应,并且它也可以促进这些菌株的毒力。在分离物中观察到基因型的巨大差异,这可能表明获得的社区感染的不同来源。

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