Firoozeh Farzaneh, Mahluji Zeinab, Shams Ehsaneh, Khorshidi Ahmad, Zibaei Mohammad
Department of Microbiology and Immunology, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Department of Microbiology and Immunology, School of Medicine, Karaj University of Medical Sciences, Karaj, Iran.
Iran J Microbiol. 2017 Oct;9(5):283-287.
New Delhi metallo-ß-lactamase (NDM) is a newly emerging metallo-ß-lactamases, which can destroy all β-lactams including carbapenems. Therefore, this study aimed at evaluating New Delhi metallo-ß-lactamase-1-production in clinical isolates of in Kashan, Iran.
In a cross-sectional study, 181 isolates were collected from clinical samples of patients, who referred to Shahid Beheshi hospital in Kashan during November 2013 and October 2014. Antimicrobial susceptibility patterns were determined using disk diffusion method, according to CLSI guidelines. Metallo-ß-lactamase (MBL) production was identified among imipenem-resistant isolates using imipenem-EDTA double disk synergy test (EDTA-IMP DDST). PCR method and sequencing were used to detect integron Class 1 and gene. Statistical analyses were performed using SPSS software Version 16.
Of the 181 isolates, 36 (19.9 %) were imipenem-resistant strains. A total of 28 out of 36 (77.7%) imipenem-resistant isolates were identified as MBL producer strains. Also, 150 (82.9%) isolates carried gene, and 20 (11.1%) isolates harbored gene.
Our study revealed a high frequency of MBL production and the presence of among strains, especially among hospitalized patients, which is alarming. Moreover, the presence of Class 1 integrons in all multi-drug resistant isolates highlights the risk of rapid spread of the resistance genes, especially in clinical settings.
新德里金属β-内酰胺酶(NDM)是一种新出现的金属β-内酰胺酶,它能破坏包括碳青霉烯类在内的所有β-内酰胺类抗生素。因此,本研究旨在评估伊朗卡尚临床分离株中新型德里金属β-内酰胺酶-1的产生情况。
在一项横断面研究中,从2013年11月至2014年10月转诊至卡尚沙希德·贝赫什提医院的患者临床样本中收集了181株分离株。根据美国临床和实验室标准协会(CLSI)指南,采用纸片扩散法测定抗菌药物敏感性模式。使用亚胺培南-乙二胺四乙酸双纸片协同试验(EDTA-IMP DDST)在耐亚胺培南的分离株中鉴定金属β-内酰胺酶(MBL)的产生情况。采用聚合酶链反应(PCR)方法和测序来检测1类整合子和NDM基因。使用SPSS 16.0软件进行统计分析。
在181株分离株中,36株(19.9%)为耐亚胺培南菌株。在36株耐亚胺培南菌株中,共有28株(77.7%)被鉴定为产MBL菌株。此外,150株(82.9%)分离株携带NDM基因,20株(11.1%)分离株含有1类整合子。
我们的研究显示,尤其是在住院患者中,MBL产生的频率很高,并且在鲍曼不动杆菌菌株中存在NDM基因,这令人担忧。此外,所有多重耐药鲍曼不动杆菌分离株中1类整合子的存在突出了耐药基因快速传播的风险,尤其是在临床环境中。