碳青霉烯酶基因blaNDM、blaVIM、blaKPC和blaOXA-48在铜绿假单胞菌临床分离株中的共现

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International Journal of Biomedicine Pub Date : 2023-09-05 DOI:10.21103/article13(3)_oa12
S. Mohamed, Zainab Ahmed, Tajalseer Mubarak, Sara Mohamed, Rayan Mohamed, H. Higazi, Sara Ali
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引用次数: 0

摘要

铜绿假单胞菌是一种革兰氏阴性菌,因其对许多抗生素的先天耐药性而臭名昭著。碳青霉烯类是一种广谱抗生素,常用于治疗严重的铜绿假单胞菌感染。然而,耐碳青霉烯P. aeruginosa (CRPA)菌株的出现和增殖已经成为一个严重的全球健康问题。本研究检测了四种主要碳青霉烯酶基因blaNDM、blaVIM、blaKPC和blaOXA-48在铜绿假单胞菌临床分离株中的共现情况。采用标准的微生物学方法,收集并鉴定了150株铜绿假单胞菌临床分离株,并按照临床和实验室标准协会的指南进行了抗菌药敏试验。采用基因特异性引物聚合酶链反应(PCR)检测碳青霉烯酶基因的存在。在150株铜绿假单胞菌临床分离株中,发现62株(41.3%)对碳青霉烯耐药。检出最多的碳青霉烯酶基因为blaKPC(49%)、blaNDM(31%)、blaOXA-48(22%)和blaVIM(9%)。值得注意的是,13株(12.9%)分离株携带两个碳青霉烯酶基因。在8株分离株中发现blaKPC和blaNDM基因结合,2株分离株携带blaKPC和blaVIM基因,3株分离株携带blaOXA-48和blaNDM基因。4株(6.5%)含有3个碳青霉烯酶基因。4株(2.8%)共出现blaNDM、blaVIM、blaKPC和blaOXA-48。我们的发现强调了碳青霉烯酶基因的惊人流行,特别是blaNDM和blaKPC,在铜绿假单胞菌的临床分离株中。多个碳青霉烯酶基因同时出现在同一株分离物中,引起了人们对多重耐药铜绿假单胞菌菌株在临床环境中可能发生水平基因转移和传播的担忧。碳青霉烯酶基因共存的分子机制及其对铜绿假单胞菌感染临床结果的影响有待进一步研究。当务之急是采取紧急措施,如加强监测、感染控制协议和抗生素管理计划,以对抗CRPA菌株的出现和传播。
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Co-occurrence of Carbapenemase Genes blaNDM, blaVIM, blaKPC and blaOXA-48 in Pseudomonas aeruginosa Clinical Isolates
Pseudomonas aeruginosa, a gram-negative bacterium, is notorious for its innate resistance to many antibiotics. Carbapenems are broad-spectrum antibiotics often used to treat severe P. aeruginosa infections. However, the emergence and proliferation of carbapenem-resistant P. aeruginosa (CRPA) strains have become a grave global health concern. This study examined the co-occurrence of four major carbapenemase genes, namely blaNDM, blaVIM, blaKPC, and blaOXA-48, in clinical isolates of P. aeruginosa. Using standard microbiological methods,150 P. aeruginosa clinical isolates were collected and identified, and antimicrobial susceptibility testing was conducted following Clinical and Laboratory Standards Institute guidelines. Polymerase chain reaction (PCR) with gene-specific primers was used to detect the presence of carbapenemase genes. Among the 150 P. aeruginosa clinical isolates, 62(41.3%) were found to be carbapenem-resistant. The most detected carbapenemase genes were blaKPC (49%), blaNDM (31%), blaOXA-48 (22%), and blaVIM (9%). Notably 13(12.9%) isolates carried two carbapenemase genes. The combination of blaKPC and blaNDM genes was found in eight isolates, two isolates carried blaKPC and blaVIM, and three isolates carried blaOXA-48 and blaNDM. Four isolates (6.5%) harbored three carbapenemase genes. Co-occurrence of blaNDM, blaVIM, blaKPC, and blaOXA-48 was observed in four isolates (2.8%). Our findings highlight the alarming prevalence of carbapenemase genes, particularly blaNDM and blaKPC, in clinical isolates of P. aeruginosa. The co-occurrence of multiple carbapenemase genes in the same isolate raises concerns about the potential for horizontal gene transfer and dissemination of multidrug-resistant P. aeruginosa strains in clinical settings. Further research is needed to elucidate the molecular mechanisms underlying the co-occurrence of carbapenemase genes and their impact on the clinical outcomes of P. aeruginosa infections. Urgent measures, such as enhanced surveillance, infection control protocols, and antibiotic stewardship programs, are imperative to combat the emergence and spread of CRPA strains.
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来源期刊
International Journal of Biomedicine
International Journal of Biomedicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
0.60
自引率
33.30%
发文量
90
审稿时长
8 weeks
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