某三甲医院新生儿ST692型NDM-5和OXA-181联产大肠埃希菌血流感染流行病学特征

Epidemiological characteristics of neonatal bloodstream infection with Escherichia coli ST692 coproducing NDM-5 and OXA-181 in a tertiary hospital

  • 摘要:
    目的  探讨ST692型NDM-5和OXA-181联产碳青霉烯酶大肠埃希菌血流感染的流行病学特征,为临床合理使用抗菌药物提供参考依据。
    方法  收集某三级甲等医院2022年3-6月新生儿血流感染分离的碳青霉烯耐药大肠埃希菌(CRECO),采用微量肉汤稀释法进行抗菌药物最小抑菌浓度(MIC)测定,采用改良Hodge试验、改良碳青霉烯灭活试验(mCIM)和乙二胺四乙酸碳青霉烯灭活试验(eCIM)检测碳青霉烯酶,采用聚合酶链式反应(PCR)检测碳青霉烯酶基因(blaKPCblaNDMblaVIMblaIMPblaOXA-48),采用多位点序列分型(MLST)和脉冲场凝胶电泳(PFGE)方法检测其同源性。
    结果  2022年3-6月分离出17株CRECO,其中发现4株血流感染CRECO,均来自新生儿监护室,其中有3株是blaNDM-5blaOXA-181联产的CRECO,为ST692型;3株联产碳青霉烯酶的CRECO菌株对头孢菌素类、喹诺酮类、复方磺胺类、碳青霉烯类100.00%耐药,对四环素类、多肽类和氨基糖苷类均敏感;同源性分析显示,3株联产血流感染CRECO菌株高度同源。
    结论  3株blaNDM-5blaOXA-181联产的CRECO菌株对多种抗菌药物均呈现高水平耐药,均为ST692型,应当加强对此类碳青霉烯酶联产菌株的检测,控制此类细菌在医疗机构内的流行。

     

    Abstract:
    OBJECTIVE  To investigate the epidemiological characteristics of bloodstream infections caused by Escherichia coli ST692 co-producing NDM-5 and OXA-181 carbapenemases, and to provide a reference for the rational use of antimicrobial agents in clinical practice.
    METHODS  From Mar. to Jun. 2022, carbapenem-resistant Escherichia coli (CRECO) strains isolated from infected neonatal bloodstream in a tertiary hospital were collected. The minimum inhibitory concentrations (MIC) of antimicrobial agents were determined by the microbroth dilution method. Carbapenemases were tested by the modified Hodge test, modified carbapenem inactivation method(mCIM) and ethylenediaminetetraacetic acid-carbapenem inactivation method(eCIM). Carbapenemase genes (blaKPC, blaNDM, blaVIM, blaIMP, blaOXA-48) were detected by polymerase chain reaction(PCR), and homogeneity was assessed by multilocus sequence typing (MLST) and pulsed-field gel electrophoresis (PFGE).
    RESULTS  Of 17 CRECO strains isolated from Mar. to Jun. 2022, four were identified in bloodstream from the neonatal intensive care unit. Three of them were ST692 coharboring blaNDM-5 and blaOXA-181, which were 100.00% resistant to cephalosporins, quinolones, sulfonamides and carbapenems, but sensitive to tetracyclines, polypeptides and aminoglycosides. Homogeneity analysis showed that the three strains were highly homologous.
    CONCLUSION  The three strains of CRECO were all ST692 co-harboring blaNDM-5 and blaOXA-181 and exhibited high resistance to multiple antimicrobial agents. There is a need to strengthen the targeted detection of such type of strains and control its prevalence in healthcare institutions.

     

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