西安地区87株艰难梭菌分子流行病学特征

Molecular epidemiological characteristics of 87 Clostridioides difficile isolates in Xi′an region

  • 摘要:
    目的 了解西安地区艰难梭菌的分子流行病学特征、抗菌药物敏感性和耐药机制,为防控艰难梭菌感染和临床合理应用抗菌药物提供数据支持。
    方法 对2018年10月-2022年12月从6家医院收集腹泻标本并成功分离的87株艰难梭菌进行毒力基因的检测,多位点序列分型(MLST)和核糖体分型(RT)方法分析艰难梭菌的种群结构和遗传多样性,采用Etest药敏条方法检测药物敏感性并检测喹诺酮耐药决定区GyrA和GyrB的氨基酸变异。
    结果 产毒艰难梭菌基因型A+B+CDT-41株,占62.12%;A-B+CDT-23株,占34.85%;A+B+CDT+2株,占3.03%。MLST共分为25个ST型别,主要型别为ST3、ST42和ST39等;核糖体分型共37种RT型别,主要型别为RT012、RT106等。所有菌株对万古霉素和甲硝唑敏感,对环丙沙星、左氧氟沙星和莫西沙星耐药率分别为90.80%、28.73%和21.84%。GyrA含Thr82-Ile和Asp205-Glu2种氨基酸变异,GyrB有6种氨基酸变异。
    结论 西安地区艰难梭菌产毒株以A+B+CDT-为主要型别,分子型别主要为ST54/RT012、ST42/RT106、ST3/RT001和ST37/RT017。未发现对万古霉素和甲硝唑耐药的菌株,艰难梭菌GyrA或GyrB中氨基酸变异与喹诺酮耐药有关,为有效预防艰难梭菌感染暴发流行,需要进一步加强分子流行病学及耐药监测工作。

     

    Abstract:
    OBJECTIVE To understand the molecular epidemiological characteristics, antimicrobial sensitivity and resistance mechanisms of Clostridioides difficile in Xi′an region, and provide data support for the prevention and control of C. difficile infection and the rational clinical use of antibiotics.
    METHODS A total of 87 strains of C. difficile, which were successfully isolated from stool samples collected from 6 hospitals from Oct. 2018 to Dec. 2022, were tested for virulence genes, population structure and genetic diversity were detected by Multilocus sequence typing (MLST) and Ribotyping (RT) methods, the drug sensitivity was detected by Etest, additionally, amino acid variations in the quinolone resistance-determining regions GyrA and GyrB were detected.
    RESULTS There were 41 strains (62.12%) with the genotype A+B+CDT-, 23 strains (34.85%) with the genotype A-B+CDT-, and 2 strains (3.03%) with the genotype A+B+CDT+. MLST was divided into 25 ST types, and the main types were ST3, ST42 and ST39. There were 37 RT types, mainly were RT012, RT106 and RT001. All strains were sensitive to vancomycin and metronidazole, and the resistance rates to ciprofloxacin, levofloxacin and moxifloxacin were 90.80%, 28.73% and 21.84%, respectively. GyrA contains two amino acid variations at Thr82-Ile and Asp205-Glu, and GyrB contains 6 amino acid variations.
    CONCLUSIONS The predominant toxin-producing strain of C. difficile in Xi′an is of A+B+CDT- genotype and the primary molecular types are ST54/RT012, ST42/RT106, ST3/RT001 and ST37/RT017. No strains resistant to vancomycin or metronidazole are detected. Amino acid variations in GyrA or GyrB of C. difficile are associated with quinolone resistance. To effectively prevent the outbreak of C. difficile infection, it is crucial to enhance molecular epidemiology studies and strengthen antimicrobial resistance surveillance efforts.

     

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