检验医学 ›› 2020, Vol. 35 ›› Issue (10): 994-999.DOI: 10.3969/j.issn.1673-8640.2020.10.007

• 碳青霉烯类耐药肠杆菌科细菌临床检测与治疗方案的发展及应用专题 • 上一篇    下一篇

Polymyxin NP实验筛查肠杆菌科多黏菌素耐药菌株临床评价

唐瑜1, 沈平华2, 史保庆3, 蒋晓飞4()   

  1. 1.上海交通大学附属胸科医院检验科,上海 200030
    2.上海市第一妇婴保健院检验科,上海 200040
    3.枣庄市市中区矿务局医院检验科,山东 枣庄 277100
    4.复旦大学附属华山医院检验科,上海 200040
  • 收稿日期:2019-07-25 出版日期:2020-10-30 发布日期:2020-11-12
  • 作者简介:null
    作者简介:唐 瑜,女,1991年生,博士,技师,主要从事革兰阴性菌耐药机制研究。
  • 基金资助:
    国家自然科学基金资助项目(81871692);国家自然科学基金资助项目(81572031)

Clinical evaluation of Polymyxin NP test for screening polymyxin-resistant Enterobacteriaceae

TANG Yu1, SHEN Pinghua2, SHI Baoqing4, JIANG Xiaofei4()   

  1. 1. Department of Clinical Laboratory,Shanghai Chest Hospital,Shanghai 200030,China
    2. Department of Clinical Laboratory,Shanghai First Maternal and Infant Hospital,Shanghai 200040,China
    3. Department of Clinical Laboratory,Zaozhuang Hospital of Zaozhuang Mining Group,Zaozhuang 277100,Shandong,China
    4. Department of Clinical Laboratory,Huashan Hospital,Fudan University,Shanghai 200040,China
  • Received:2019-07-25 Online:2020-10-30 Published:2020-11-12

摘要:

目的 评价Polymyxin NP实验筛查多黏菌素耐药肠杆菌科细菌的临床价值。方法 采用Polymyxin NP实验对461株肠杆菌科临床分离株进行初步筛查,采用微量肉汤稀释法测定菌株对多黏菌素的最小抑菌浓度(MIC),采用纸片扩散法进行临床常用抗菌药物的体外药物敏感性试验,采用聚合酶链反应(PCR)扩增多黏菌素耐药相关基因pmrApmrBphoPphoQmgrBmcr,并进行测序,采用实时定量聚合酶链反应(qRT-PCR)检测多黏菌素耐药相关双组分调控元件pmrA/pmrBpmrD/pmrFPhoP/PhoQ表达水平。结果 461株肠杆菌科细菌中,13株多黏菌素耐药株Polymyxin NP实验在2 h内均表现为阳性,多黏菌素敏感菌株表现为阴性。13株多黏菌素耐药菌株中,10株肺炎克雷伯菌主要由mgrB基因插入突变及双组分调控系统pmrA/pmrBPhoP/PhoQ突变或表达上调引起,1株大肠埃希菌由质粒携带的mcr-1基因介导,2株阴沟肠杆菌的耐药机制尚不清楚。多黏菌素耐药菌株和敏感菌株对多种常用抗菌药物的耐药率差异无统计学意义(P>0.05)。结论 Polymyxin NP实验操作简便、结果可靠,可用于各种机制介导的多黏菌素耐药肠杆菌科细菌的临床筛查,为临床抗感染治疗和耐药防控提供依据。

关键词: 肠杆菌科, Polymyxin NP实验, 多黏菌素耐药

Abstract:

Objective To evaluate the clinical role of Polymyxin NP test for screening polymyxin-resistant Enterobacteriaceae. Methods A total of 461 isolates of Enterobacteriaceae were screened by Polymyxin NP test preliminarily. Broth microdilution method was performed to determine minimum inhibitory concentration(MIC) of polymyxin,and Kirby-Bauer method was used to determine the in vitro antimicrobial susceptibility of common antibiotics. Polymyxin-related genes,including pmrA,pmrB,phoP,phoQ,mgrB and mcr,were determined by polymerase chain reaction(PCR) and sequencing. Real-time quantitative polymerase chain reaction(qRT-PCR) was performed to determine the expression levels of genes associated with pmrA/pmrB,pmrD/pmrF and PhoP/PhoQ regulatory systems. Results Among the 461 Enterobacteriaceae isolates,within 2 h,13 polymyxin-resistant isolates were positive in Polymyxin NP test,and polymyxin-susceptible isolates were negative. Totally,10 of 13 polymyxin-resistant isolates belonging to Klebsiella pneumoniae resulted from insertion of mgrB as well as mutants and expression increasing of pmrA/pmrB and PhoP/PhoQ regulatory systems,and 1 isolate belonging to Escherichia coli was mediated bymcr-1 in plasmid. The resistance mechanisms of 2 isolates of Enterobacter cloacae were still unclear. There was no statistical significance between polymyxin-resistant and polymyxin-susceptible isolates(P>0.05). Conclusions Polymyxin NP test is easy to perform and reliable. It could be used in screening polymyxin-resistant Enterobacteriaceae mediated by various mechanisms,which can provide a reference for treating infectious diseases and preventing the prevalence of resistance.

Key words: Enterobacteriaceae, Polymyxin NP test, Polymyxin resistance

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