设计一种快速准确检测伊朗德黑兰鲍曼不动杆菌金属β -内酰胺酶耐药基因的多重PCR方法

Q3 Medicine
zahra Mottaghiyan, Davoud Esmaeili, Mohammad Ahmadi, Mohammad Niakan
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引用次数: 0

摘要

背景与目的:鲍曼不动杆菌携带的Meallobetalactamases (MBL)在医院感染中构成重大威胁。本研究的目的是设计一种多重PCR方法,用于同时检测伊朗德黑兰市流行的鲍曼不动杆菌菌株的MBL基因。方法:2020年10月至2021年2月,从德黑兰Motahhari医院住院患者的烧伤标本中采集100株鲍曼不动杆菌。鲍曼不动杆菌菌株的鉴定采用常规生化技术,同时确认了bla OXA-51基因的存在。采用Kirby-Bauer椎间盘扩散试验评估抗生素敏感性。采用联合圆盘试验对产生mbl的菌株进行表型鉴定,并采用多重PCR同时鉴定bla VIM、bla IMP、bla GIM和bla NDM基因。统计学分析采用卡方检验,数据处理采用SPSS 20.0版本。结果:在100株菌株中,96.1%的菌株MBL检测呈阳性。该研究揭示了广泛耐药(XDR)菌株的优势,粘菌素显示出最高水平的敏感性。基因型分析结果显示,20株菌株中存在bla VIM、bla NDM和bla IMP基因,30株菌株中存在bla VIM和bla NDM基因,45株菌株中只存在bla NDM基因。值得注意的是,多重PCR技术能够同时检测2个菌株的MBL基因(bla VIM、bla IMP、bla GIM、bla NDM)。结论:目前的调查强调了bla NDM基因在鲍曼不动杆菌临床菌株中的流行。此外,多重PCR作为一种快速识别鲍曼不动杆菌MBL基因的强大且高度敏感的技术出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Designing a Multiplex PCR for Rapid and Accurate Detection of Metallobetalactamases Resistant Genes from Acinetobacter baumaniiIsolates in Tehran City, Iran
Background & Objective: Acinetobacter baumannii strains harboring Meallobetalactamases (MBL) pose a significant threat in the context of nosocomial infections. The present investigation was undertaken with the objective of devising a Multiplex PCR methodology for the concurrent detection of MBL genes within A. baumannii strains prevalent in Tehran City, Iran.Methods: Between October 2020 and February 2021, 100 strains of A. baumannii were procured from burn specimens of hospitalized patients at Motahhari Hospital in Tehran. The identification of A. baumannii strains involved conventional biochemical techniques, coupled with confirmation of the presence of the bla OXA-51 gene. Antibiotic susceptibility was assessed using the Kirby–Bauer disc diffusion test. MBL-producing strains were characterized through a phenotypic approach employing the combined disk test, alongside Multiplex PCR for the simultaneous identification of bla VIM, bla IMP, bla GIM, and bla NDM genes. Statistical analyses were conducted using the chi-square test, with SPSS version 20.0 employed for data processing.Results: Among 100 strains examined, 96.1% exhibited positivity for MBL, as determined by the combined disk test. The study revealed a predominance of extensively drug-resistant (XDR) strains, with colistin demonstrating the highest level of sensitivity. The genotypic assay unveiled that Multiplex PCR identified bla VIM, bla NDM, and bla IMP in 20 strains, bla VIM and bla NDM in 30 strains, and exclusively the bla NDM gene in 45 strains. Notably, the Multiplex PCR technique exhibited the capacity to concurrently detect MBL genes (bla VIM, bla IMP, bla GIM, bla NDM) in 2 strains.Conclusion: The current investigation underscores prevalence of the bla NDM gene within clinical strains of A. baumannii. Furthermore, Multiplex PCR emerges as a robust and highly sensitive technique for rapid discernment of the MBL genes within in A. baumannii strains.
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来源期刊
Iranian Journal of Pathology
Iranian Journal of Pathology Medicine-Pathology and Forensic Medicine
CiteScore
2.00
自引率
0.00%
发文量
99
审稿时长
20 weeks
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