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利奈唑胺耐药屎肠球菌分离株的耐药机制和临床特征:韩国单中心研究。

Resistance mechanisms and clinical characteristics of linezolid-resistant Enterococcus faecium isolates: A single-centre study in South Korea.

机构信息

Division of Infectious Diseases, Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea; Center for Infection Prevention and Control, Samsung Medical Center, Seoul, South Korea.

Asia Pacific Foundation for Infectious Diseases (APFID), Seoul, South Korea.

出版信息

J Glob Antimicrob Resist. 2018 Mar;12:44-47. doi: 10.1016/j.jgar.2017.09.009. Epub 2017 Sep 20.

Abstract

OBJECTIVES

This study aimed to determine the prevalence of linezolid-resistant (LR) vancomycin-resistant enterococci and to investigate the mechanisms of linezolid resistance with clinical and microbiological characterisation.

METHODS

All vancomycin-resistant Enterococcus faecium (VREF) isolated from blood and rectal swab cultures during 2012-2015 were tested for linezolid resistance. LR-VREF isolates were tested for antimicrobial susceptibility, glycopeptide resistance genes and virulence genes. Multilocus sequence typing (MLST) and pulsed-field gel electrophoresis (PFGE) were performed. Isolates were tested for known mechanisms of linezolid resistance.

RESULTS

Among 389 VREF isolates, 7 (1.8%) were found to be resistant to linezolid. All LR-VREF isolates carried the vanA gene. Five isolates had both hyl and esp genes. The isolates were susceptible to tigecycline, daptomycin and quinupristin/dalfopristin, except for one isolate with daptomycin resistance. Two LR-VREF isolates recovered from patients with previous linezolid exposure contained the G2576T mutation in 23S rRNA and exhibited high-level resistance to linezolid (MIC>64mg/L). The other five isolates recovered from linezolid-naïve patients revealed no known linezolid resistance mechanism and exhibited low-level resistance to linezolid (MICs=8-16mg/L). Plasmid-mediated genes encoding cfr or optrA were not detected. LR-VREF isolates were represented by six different sequence types, belonging to hospital lineages, and were assigned to seven PFGE types.

CONCLUSIONS

The prevalence of LR-VREF in this centre was low. Both linezolid exposure and horizontal transmission appear to be responsible for acquisition of LR-VREF in hospitalised patients. Prudent use of linezolid and improved infection control strategies are needed to limit the spread of LR-VREF.

摘要

目的

本研究旨在确定耐(linezolid-resistant, LR)利奈唑胺的万古霉素耐药肠球菌(vancomycin-resistant enterococci, VRE)的流行率,并通过临床和微生物学特征研究利奈唑胺耐药的机制。

方法

对 2012 年至 2015 年期间从血液和直肠拭子培养物中分离出的所有万古霉素耐药粪肠球菌(vancomycin-resistant Enterococcus faecium, VREF)进行利奈唑胺耐药性检测。LR-VREF 分离株进行抗菌药物敏感性、糖肽类耐药基因和毒力基因检测。进行多位点序列分型(multilocus sequence typing, MLST)和脉冲场凝胶电泳(pulsed-field gel electrophoresis, PFGE)。检测已知的利奈唑胺耐药机制。

结果

在 389 株 VREF 分离株中,发现 7 株(1.8%)对利奈唑胺耐药。所有 LR-VREF 分离株均携带 vanA 基因。5 株分离株同时携带 hyl 和 esp 基因。除 1 株对达托霉素耐药的分离株外,所有分离株均对替加环素、达托霉素和奎奴普丁/达福普汀敏感。从先前利奈唑胺暴露的患者中分离出的 2 株 LR-VREF 分离株含有 23S rRNA 上的 G2576T 突变,对利奈唑胺表现出高水平耐药(MIC>64mg/L)。从利奈唑胺初治患者中分离出的另外 5 株分离株未发现已知的利奈唑胺耐药机制,对利奈唑胺表现出低水平耐药(MICs=8-16mg/L)。未检测到编码 cfr 或 optrA 的质粒介导基因。LR-VREF 分离株代表了 6 种不同的序列类型,属于医院谱系,并分为 7 种 PFGE 型。

结论

本中心 LR-VREF 的流行率较低。利奈唑胺暴露和水平传播似乎都导致了住院患者中 LR-VREF 的获得。需要谨慎使用利奈唑胺和改进感染控制策略,以限制 LR-VREF 的传播。

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