Evaluation of Plasmid Mediated Colistin Resistance in Colistin Resistant Gram-negative Bacilli

Y. Tanrıverdi Çaycı, Kubra Hacieminoglu Ulker, Demet Gur Vural, K. Bilgin, A. Birinci
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Abstract

Background: Infections caused by carbapenem-resistant gram-negative bacteria are treated with colonistin as a last resort. However, the increased resistance in recent years is significant for treating multiple drug-resistant infections. Objectives: This study aimed to determine the resistance genes mobile colistin resistance (mcr)-1 and mcr-2 in the colistin-resistant isolates, understand the resistance mechanism, and help with treatment. Methods: Isolates were identified in the Vitek MS automated system. The antibiotic susceptibility was tested with the Vitek 2 Compact automated system. Enteric gram-negative bacilli isolates were stored at -20°C until the molecular study. DNA extraction of colistin-resistant isolates was performed by boiling method. Then, polymerase chain reaction (PCR) optimization was performed using the specific primers, and mcr-1 and mcr-2 genes were investigated by the multiplex PCR method. Results: About 170 enteric gram-negative bacilli isolate were mainly sent from internal medicine (44.7%) and neurology (13.5%) services. According to the species identification, 37.6% of the isolates were Klebsiella pneumonia, and 31.7% were Serratia marcescens. Based on PCR results, mcr-1 and mcr-2 genes were not detected in the isolates. Conclusions: Increased colistin resistance and the worrying discovery of mcr genes require urgent precautions, even though the study did not detect mcr-1 and mcr-2. New studies investigating mcr genes in new isolates are needed to understand the mechanism of resistance and identify resistant isolates.
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耐粘菌素革兰氏阴性杆菌质粒介导的粘菌素耐药性评价
背景:碳青霉烯耐药革兰氏阴性菌引起的感染是最后的治疗手段。然而,近年来耐药性的增加对治疗多重耐药感染具有重要意义。目的:检测黏菌素耐药菌株的耐药基因mcr -1和mcr-2,了解其耐药机制,为治疗提供依据。方法:分离物在Vitek MS自动系统中鉴定。使用Vitek 2 Compact自动系统进行抗生素敏感性测试。分离的肠内革兰氏阴性杆菌保存在-20°C以待分子研究。采用煮沸法提取耐粘菌素菌株的DNA。然后利用特异性引物进行聚合酶链反应(PCR)优化,并采用多重PCR法对mcr-1和mcr-2基因进行检测。结果:170株肠源性革兰氏阴性杆菌主要来自内科(44.7%)和神经内科(13.5%)。根据菌种鉴定,肺炎克雷伯菌占37.6%,粘质沙雷菌占31.7%。PCR结果显示,分离株中未检出mcr-1和mcr-2基因。结论:尽管该研究未检测到mcr-1和mcr-2,但增加的粘菌素耐药性和令人担忧的mcr基因发现需要紧急预防。需要对新分离株的mcr基因进行新的研究,以了解耐药机制并鉴定耐药分离株。
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