肺炎克雷伯菌临床分离株中广谱β -内酰胺酶产生的流行和特征

B. Fouzia, A. Damle
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引用次数: 6

摘要

目的:研究TEM和SHV基因在产β-内酰胺酶(ESBL)肺炎克雷伯菌中的存在。本研究还旨在比较表型验证性双盘扩散试验和基因型方法的结果。材料与方法:选取2012年6月至2013年12月共679株肺炎克雷伯菌进行研究。采用Kirby - Bauer纸片扩散法测定耐药模式。筛选ESBL,经表型确证性椎间盘扩散试验(PCDDT)证实。随机选取100株分离株,采用两组不同引物,采用聚合酶链反应(PCR)检测TEM和SHV基因的存在。对其进行多重PCR检测。结果:表型证实试验能检测出90.13%的肺炎克雷伯菌分离株产生ESBL。在两种ESBL基因型中,TEM基因型最为普遍。大多数产生ESBL的分离株同时具有ESBL基因。结论:多重PCR可作为一种快速鉴定肺炎克雷伯菌产生广谱β -内酰胺酶的共同基因(TEM和SHV)的方法。它将证明对监测和确定针对耐药生物体的治疗路线是有价值的,从而节省宝贵的时间和资源。PCDDT检测结果均与基因型法相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence and Characterization of Extended Spectrum Beta-Lactamase Production in Clinical Isolates of Klebsiella pneumonia
Aim: This study was carried out to determine the presence of TEM and SHV genes in extended- spectrum β-lactamase (ESBL) producing Klebsiella pneumoniae. The study was also aimed to compare results of phenotypic confirmatory double disc diffusion test and genotypic methods. Materials and Methods: A total of 679 strains of Klebsiella pneumoniae were selected for the study from June 2012-December 2013. Kirby – Bauer disk diffusion method was performed to determine the antibiotic resistance pattern. Screened for ESBL and confirmed by phenotypic confirmatory disc diffusion test (PCDDT). 100 randomly selected isolates were investigated for the presence of TEM and SHV genes via Polymerase chain reaction (PCR) using two different sets of primers. Multiplex PCR was also performed for the same. Results: Phenotypic confirmatory test was able to detect ESBL production in 90.13% of Klebsiella pneumoniae isolates. Among the two ESBL genotypes, the most prevalent genotype was found to be TEM. Majority of ESBL producing isolates possess both ESBL genes. Conclusion: Multiplex PCR can be used as a rapid method to identify common genes (TEM and SHV) responsible for extended spectrum beta lactamase production in Klebsiella pneumoniae. It will prove valuable for surveillance and for determining the line of treatment against drug resistant organisms, thus saving precious time and resources. PCDDT results correlated with genotypic method in all the tested strains.
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