Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran.
Department of Microbiology, Research Center of Health Reference Laboratory, Ministry of Health and Medical Education, Tehran, Iran.
BMC Microbiol. 2024 Jun 28;24(1):230. doi: 10.1186/s12866-024-03376-4.
Carbapenemase-producing Klebsiella pneumoniae (CRKP) presents a significant challenge to antimicrobial therapy, especially when compounded by resistance to colistin. The objective of this study was to explore molecular epidemiological insights into strains of clinical K. pneumoniae that produce carbapenemases and exhibit resistance to colistin. Eighty clinical isolates of CRKP were obtained from Milad Hospital in Tehran, Iran. Antimicrobial susceptibility and colistin broth disk elution were determined. PCR assays were conducted to examine the prevalence of resistance-associated genes, including bla, bla, bla, bla, bla and mcr-1 to -10. Molecular typing (PFGE) was used to assess their spread.
Colistin resistance was observed in 27 isolates (33.7%) using the Broth Disk Elution method. Among positive isolates for carbapenemase genes, the most frequent gene was bla, identified in 36 strains (45%). The mcr-1 gene was detected in 3.7% of the obtained isolates, with none of the other of the other mcr genes detected in the studied isolates.
To stop the spread of resistant K. pneumoniae and prevent the evolution of mcr genes, it is imperative to enhance surveillance, adhere rigorously to infection prevention protocols, and implement antibiotic stewardship practices.
产碳青霉烯酶肺炎克雷伯菌(CRKP)对抗菌治疗构成重大挑战,尤其是在对黏菌素耐药的情况下。本研究旨在探讨对碳青霉烯类药物具有耐药性并对黏菌素耐药的临床肺炎克雷伯菌菌株的分子流行病学见解。从伊朗德黑兰 Milad 医院获得了 80 株临床耐碳青霉烯肺炎克雷伯菌。测定了药敏试验和黏菌素肉汤稀释法药敏纸片洗脱法。采用 PCR 检测法检测耐药相关基因 bla、bla、bla、bla、bla 和 mcr-1 至 mcr-10 的流行情况。采用 PFGE 对其传播情况进行分子分型。
采用肉汤稀释法药敏纸片洗脱法检测,27 株(33.7%)对黏菌素耐药。在检测到的产碳青霉烯酶基因阳性菌株中,最常见的基因是 bla,在 36 株(45%)中发现。在获得的分离株中检测到 mcr-1 基因的 3.7%,而在研究的分离株中未检测到其他 mcr 基因。
为了阻止耐药肺炎克雷伯菌的传播并防止 mcr 基因的进化,加强监测、严格遵守感染预防方案和实施抗生素管理实践至关重要。