Biology Research Center, Zanjan branch, Islamic Azad University, Zanjan, Iran.
Department of Clinical Microbiology, Maku branch, Islamic Azad University, Maku, Iran.
Braz J Microbiol. 2023 Sep;54(3):1769-1781. doi: 10.1007/s42770-023-01084-1. Epub 2023 Aug 21.
Quinolones are one of the most widely used drugs in medicine. Resistance to this agent has been increased significantly among the nosocomial isolates. The objective of this research was to study generalized transduction, as a potential mechanism for plasmid-mediated quinolone resistance (PMQR) genes acquisition among hospital effluent isolates. Discharge samples from hospital effluent were taken from four medical centers in Azerbaijan. Resident phages were enriched against resident enterobacterial hosts using standard phage enrichment protocols. Polymerase chain reaction (PCR) was used to examine phage stocks and bacterial isolates for the presence of PMQR determinants. All positive bacterial isolates for target genes were subjected to transduction assays. Restriction fragment length polymorphism (RFLP) profiles were determined for cluster analysis. A total of 55 pure phage stocks were prepared from 42 effluents. A total of 95 non-duplicated Gram-negative bacteria were isolated. Thirty-two EcoRV-RFLP profiles were determined for the 40 Escherichia coli phage stocks. Twenty-six of 40 (65%) E. coli phages were positive for qnrB (n = 15), qnrD (n = 7), qnrA (n = 3), and qnrC (n = 2) genes. A total of 34 (35.7%) bacterial isolates were recognized to have any PMQR genes including qnrB (n = 23), qnrD (n = 8), qnrA (n = 5), and qnrC (n = 3) genes. Present research provided a strong evidence for potential role of generalized transduction in persistence and circulation of PMQR genes in health care settings of Azerbaijan.
喹诺酮类药物是医学中应用最广泛的药物之一。该药物在医院分离株中的耐药性显著增加。本研究的目的是研究普遍转导作为质粒介导的喹诺酮耐药(PMQR)基因获得的潜在机制,特别是在医院污水分离株中。从阿塞拜疆的四个医疗中心采集医院污水排放样本。使用标准噬菌体富集方案,针对常驻肠杆菌宿主富集常驻噬菌体。聚合酶链反应(PCR)用于检查噬菌体库存和细菌分离株中是否存在 PMQR 决定因素。所有针对目标基因呈阳性的细菌分离株均进行转导测定。限制性片段长度多态性(RFLP)图谱用于聚类分析。从 42 个污水中制备了总共 55 个纯噬菌体库存。总共分离出 95 个非重复革兰氏阴性菌。对 40 个大肠杆菌噬菌体库存进行了 32 个 EcoRV-RFLP 图谱分析。40 个大肠杆菌噬菌体中有 26 个(65%)为 qnrB(n = 15)、qnrD(n = 7)、qnrA(n = 3)和 qnrC(n = 2)基因阳性。总共 34 个(35.7%)细菌分离株被鉴定出携带任何 PMQR 基因,包括 qnrB(n = 23)、qnrD(n = 8)、qnrA(n = 5)和 qnrC(n = 3)基因。本研究为普遍转导在阿塞拜疆医疗保健环境中 PMQR 基因的持久性和传播中潜在作用提供了有力证据。