印度阿萨姆邦部分地区产生 ESBL 的克雷伯氏菌临床分离株中 AmpC β-内酰胺酶的流行和分布模式

Indrani Gogoi, Shyamalima Saikia, Mohan Sharma, Amos Oloo Onyango, Minakshi Puzari, Pankaj Chetia
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引用次数: 0

摘要

产生广谱β-内酰胺酶(ESBLs)和AmpC β-内酰胺酶是临床分离的克雷伯氏菌产生多药耐药性的最常见原因。DU/Dib/ECBHR(Human)/2021-22/02)。这些菌株采集自阿萨姆邦的各种医疗机构,经鉴定具有耐药性。对这些分离物进行了抗生素敏感性筛选,并对耐多药分离物进行了表型测试,以确认ESBL和AmpC β-内酰胺酶的产生。通过聚合酶链反应(PCR)研究了 ESBL 和 AmpC β-内酰胺酶基因型的分布模式。结果表明,在 107 个耐多药(MDR)克雷伯菌属分离株中,67.28% 的分离株产 ESBL,56.07% 的分离株可能产 AmpC。PCR 结果显示,blaCTX-M 是最常见的 ESBL 基因型。在ESBL产生者中,11.11%的分离株与质粒介导的AmpC β内酰胺酶基因型共存,这表明肺炎双球菌和氧乐果中ESBL和AmpC共产生者的流行率很高,可能会引发严重的公共卫生问题。因此,定期监测临床分离株中多药耐药性的传播至关重要。
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 distribution pattern of AmpC β-lactamases in ESBL producing clinical isolates of Klebsiella spp. in parts of Assam, India

Prevalence and distribution pattern of AmpC β-lactamases in ESBL producing clinical isolates of Klebsiella spp. in parts of Assam, India

The production of extended-spectrum β-lactamases (ESBLs) and AmpC β-lactamases is the most common explanation of multidrug resistance in clinical isolates of Klebsiella spp. In the present study, a total of 160 isolates of Klebsiella spp. were procured from the DBT-NER project with ethical clearance no. DU/Dib/ECBHR(Human)/2021-22/02). These were collected from various health settings of Assam and identified as drug-resistant. The isolates were screened for antibiotic susceptibility and phenotypic tests were performed on multidrug resistant isolates to confirm ESBL and AmpC β-lactamases production. The distribution pattern of ESBL and AmpC β-lactamase genotype was investigated by polymerase chain reaction (PCR). The results showed that among 107 multidrug-resistant (MDR) isolates of Klebsiella spp., 67.28% of isolates were ESBL producers and 56.07% were potential AmpC producers. The PCR results revealed that blaCTX−M was the most prevalent ESBL genotype. Among the ESBL producers, 11.11% of isolates showed co-occurrence with plasmid-mediated AmpC β lactamases genotype which indicated the high prevalence of ESBL and AmpC co-producers in K. pneumoniae and K. oxytoca, suggesting the possibility of serious public health concerns. Therefore, it is crucial to regularly monitor the spread of multidrug resistance among clinical isolates.

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