Investigation of colistin heteroresistance and the colistin resistance genes mcr-1 to mcr-5 in Escherichia coli and Klebsiella pneumoniae isolates in a tertiary hospital in Turkey.

IF 1.4 4区 医学 Q4 INFECTIOUS DISEASES Journal of Infection in Developing Countries Pub Date : 2024-11-30 DOI:10.3855/jidc.19276
Erkut Afyoncu, Canan Eryıldız
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Abstract

Introduction: Heteroresistance is not detected by traditional antimicrobial susceptibility testing methods and may lead to treatment failures. Investigating the presence of plasmid-mediated colistin resistance genes is important because of the horizontal transmission of the relevant genes between bacterial species. This study aimed to investigate the presence of colistin heteroresistance and the colistin resistance genes mcr-1 to mcr-5 in Escherichia coli and Klebsiella pneumoniae isolates.

Methodology: A total of 254 isolates, including 100 E. coli and 154 K. pneumoniae strains isolated from clinical samples, were included in the study. Colistin susceptibility was evaluated using the broth microdilution method for all strains. Heteroresistance screening was performed using the gradient strip test. Eight strains were evaluated for heteroresistance by population analysis profiling (PAP). The colistin resistance genes mcr-1 to mcr-5 were investigated by multiplex polymerase chain reaction (PCR) in colistin-resistant K. pneumoniae isolates. Multilocus sequence typing (MLST) analysis was performed on two K. pneumoniae strains.

Results: Colistin resistance was not detected in the E. coli isolates and was detected in 16.23% (25/154) of the K. pneumoniae isolates. No heteroresistant bacteria were detected by the gradient strip test or by PAP. All colistin-resistant isolates were negative for the mcr genes. The two isolates analyzed by MLST were ST14 and ST2096.

Conclusions: Periodic follow-up of colistin heteroresistance is useful for administering appropriate antibiotic therapy. In addition, the investigation of colistin resistance genes is important for infection control measures.

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土耳其某三级医院大肠杆菌和肺炎克雷伯菌分离株粘菌素异源耐药及耐药基因mcr-1 ~ mcr-5的调查
传统的药敏试验方法无法检测到异耐药,可能导致治疗失败。研究质粒介导的粘菌素耐药基因的存在是很重要的,因为相关基因在细菌物种之间是水平传播的。本研究旨在探讨大肠杆菌和肺炎克雷伯菌分离株是否存在粘菌素异源耐药及粘菌素耐药基因mcr-1 ~ mcr-5。方法:从临床标本中分离出254株,其中大肠杆菌100株,肺炎克雷伯菌154株。采用肉汤微量稀释法对所有菌株进行粘菌素敏感性评价。采用梯度条形试验进行异抗筛选。采用群体分析谱法(PAP)评价了8株菌株的异源抗性。采用多重聚合酶链反应(PCR)对耐粘菌素肺炎克雷伯菌的耐药基因mcr-1 ~ mcr-5进行了检测。对2株肺炎克雷伯菌进行多位点序列分型分析。结果:大肠杆菌中未检出粘菌素耐药,肺炎克雷伯菌中有16.23%(25/154)检出粘菌素耐药。梯度试纸法和PAP法均未检出异耐药菌。所有耐粘菌素菌株的mcr基因均为阴性。MLST分析的菌株分别为ST14和ST2096。结论:定期随访粘菌素异源耐药有助于给予适当的抗生素治疗。此外,研究粘菌素耐药基因对采取感染控制措施具有重要意义。
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来源期刊
CiteScore
3.70
自引率
5.30%
发文量
239
审稿时长
4-8 weeks
期刊介绍: The Journal of Infection in Developing Countries (JIDC) is an international journal, intended for the publication of scientific articles from Developing Countries by scientists from Developing Countries. JIDC is an independent, on-line publication with an international editorial board. JIDC is open access with no cost to view or download articles and reasonable cost for publication of research artcles, making JIDC easily availiable to scientists from resource restricted regions.
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