Malehmir Shirin, Ranjbar Reza, Harzandi Naser
Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran.
Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Open Microbiol J. 2017 Sep 21;11:189-194. doi: 10.2174/1874285801711010189. eCollection 2017.
is known as one of the most important causes of gastrointestinal disease in the world. Quinolones and fluoroquinolones are used successfully in the treatment of salmonellosis particularly for infections that have become resistant to several antibiotics. But non-susceptible isolates to quinolones have been reported in several countries. The data are limited about the prevalence of quinolone-resistant isolates in our country. Therefore, this study investigated the plasmid-mediated quinolone resistance genes in isolated in Children's Medical Center in Tehran during 2014-2015.
isolates were isolated and identified using standard microbiological methods. Antibiotic susceptibility testing and screening of strains resistant to quinolones were performed according to the CLSI guidelines. The molecular investigation was done using specific primers for detection of qnr genes including: A, B and S, by polymerase chain reaction.
Overall, 92 (66.6%) strains were resistant to nalidixic acid. None of the strains showed resistance to ciprofloxacin. Out of the 92 nalidixic acid resistant strains, 52 (56.52%) harbored S genes, 15 strains (16.30%) had both A and S genes. Two (1.1%) isolates were positive for B gene. Twenty four (26.08%) nalidixic acid resistant isolates did not have any qnr qens.
The results of this study show high prevalence of resistance to nalidixic and qnr genes in isolates. Plasmid nature of this type of resistance poses an increased risk of dissemination of quinolone resistance between and non- isolates circulating in hospitals environments.
已知是世界上胃肠道疾病的最重要病因之一。喹诺酮类和氟喹诺酮类药物成功用于治疗沙门氏菌病,特别是针对已对多种抗生素产生耐药性的感染。但在几个国家已报告了对喹诺酮不敏感的分离株。我国关于喹诺酮耐药分离株流行情况的数据有限。因此,本研究调查了2014 - 2015年期间在德黑兰儿童医学中心分离出的[细菌名称未给出]中质粒介导的喹诺酮耐药基因。
使用标准微生物学方法分离并鉴定[细菌名称未给出]分离株。根据CLSI指南进行抗生素敏感性测试和对喹诺酮耐药菌株的筛选。通过聚合酶链反应,使用检测qnr基因(包括:A、B和S)的特异性引物进行分子研究。
总体而言,92株(66.6%)对萘啶酸耐药。所有菌株对环丙沙星均未显示耐药。在92株萘啶酸耐药菌株中,52株(56.52%)携带S基因,15株(16.30%)同时具有A和S基因。2株(1.1%)分离株B基因呈阳性。24株(26.08%)萘啶酸耐药分离株没有任何qnr基因。
本研究结果显示[细菌名称未给出]分离株中对萘啶酸和qnr基因的耐药率很高。这种耐药类型的质粒性质增加了喹诺酮耐药性在医院环境中循环的[细菌名称未给出]和非[细菌名称未给出]分离株之间传播的风险。