多药耐药肺炎克雷伯菌临床分离株β -内酰胺酶基因鉴定及分子分型研究。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Azadeh Ferdosi-Shahandashti, Abazar Pournajaf, Elaheh Ferdosi-Shahandashti, Fatemeh Zaboli, Kasra Javadi
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引用次数: 0

摘要

背景:肺炎克雷伯菌是一种临床相关病原体,引起了相当大的公共卫生关注。本研究旨在确定多药耐药肺炎克雷伯菌临床分离株β -内酰胺酶基因的存在并进行分子基因分型。方法:收集巴博尔医科大学附属教育医院临床分离的耐多药肺炎克雷伯菌。通过标准的微生物和生化试验对分离的肺炎克雷伯菌进行鉴定。采用纸片扩散法、改良霍奇试验(MHT)、联合纸片法和聚合酶链反应(PCR)法评估抗生素耐药性。采用肠杆菌重复基因间一致性(ERIC)-PCR进行分子分型。结果:从各种临床标本中共分离出42株耐多药肺炎克雷伯菌。抗生素耐药性最高的是氨苄西林(100%),最低的是阿米卡星(19.04%)。MHT显示38.09%的肺炎克雷伯菌分离株产生碳青霉烯酶。54.76%的分离菌株产生金属β -内酰胺酶(MBL)。β -内酰胺酶基因分子检测显示存在blaNDM(21.42%)、blaKPC(42.85%)、blaTEM(76.19%)、blaSHV(47.16%)和blaCTX-M(80.95%)基因。ERIC-PCR分子分型鉴定出7种不同的遗传模式。结论:本调查显示肺炎克雷伯菌具有较高的耐药水平。频率最高和最低的β -内酰胺酶基因分别对应于blaCTX-M和blaNDM基因。ERIC-PCR树状图提示肺炎克雷伯菌临床分离株和医院病房内类似克隆的传播具有共同起源。这些发现表明,肺炎克雷伯菌分离株具有高毒力,需要开发更有效的抗药技术和基因转移研究。临床试验号:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of beta-lactamase genes and molecular genotyping of multidrug-resistant clinical isolates of Klebsiella pneumoniae.

Background: Klebsiella pneumoniae is a clinically relevant pathogen that has raised considerable public health concerns. This study aims to determine the presence of beta-lactamase genes and perform molecular genotyping of multidrug-resistant (MDR) K. pneumoniae clinical isolates.

Methods: Clinical isolates of MDR K. pneumoniae were collected from educational hospitals affiliated with Babol University of Medical Sciences. The isolates of K. pneumoniae were identified through standard microbial and biochemical tests. Antibiotic resistance was assessed using disk diffusion, modified Hodge test (MHT), combined disk, and polymerase chain reaction (PCR) methods. Enterobacterial Repetitive Intergenic Consensus (ERIC)-PCR was performed for molecular typing.

Results: A total of 42 MDR K. pneumoniae isolates were obtained from various clinical specimens. The highest antibiotic resistance was observed for ampicillin (100%), while the lowest resistance was noted for amikacin (19.04%). The MHT indicated that 38.09% of K. pneumoniae isolates produced carbapenemase enzymes. Metallo-beta-lactamase (MBL) production was found in 54.76% of isolates. Molecular detection of beta-lactamase genes revealed the presence of blaNDM (21.42%), blaKPC (42.85%), blaTEM (76.19%), blaSHV (47.16%), and blaCTX-M (80.95%) genes. ERIC-PCR molecular typing identified seven distinct genetic patterns among the isolates.

Conclusions: This investigation demonstrates the high resistance levels of K. pneumoniae strains. The beta-lactamase genes with the highest and lowest frequencies correspond to blaCTX-M and blaNDM genes, respectively. ERIC-PCR dendrograms suggest a common origin for K. pneumoniae clinical isolates and the propagation of similar clones within hospital wards. These findings indicate that K. pneumoniae isolates are highly virulent, necessitating the development of more effective resistance-fighting techniques and gene transfer research.

Clinical trial number: Not applicable.

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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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