中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2008年
47期
3319-3324
,共6页
王玉明%刘玉村%万远廉%刘树林%刘桂荣%汪欣%王秋实%曹小利
王玉明%劉玉村%萬遠廉%劉樹林%劉桂榮%汪訢%王鞦實%曹小利
왕옥명%류옥촌%만원렴%류수림%류계영%왕흔%왕추실%조소리
假单胞菌属,铜绿%监护%基因组,细菌
假單胞菌屬,銅綠%鑑護%基因組,細菌
가단포균속,동록%감호%기인조,세균
Pseudomonas,aeruginosa%Custodial care%Genome,bacterial
目的 对比分析外科重症监护室多重耐药铜绿假单胞菌的基因组差异,探索其与多重耐药性的关系.方法 琼脂稀释法检测49株铜绿假单胞菌对临床常用9种抗菌药物的敏感性,应用4种稀有位点核酸内切酶结合的脉冲场凝胶电泳技术(PFGE)对临床分离的株铜绿假单胞菌进行基因组分型.结果 多重耐药铜绿假单胞菌菌株占外科重症监护室铜绿假单胞菌临床分离株的85.7%;PFGE基因组型A菌株占全部铜绿假单胞菌分离株的61.2%,为主导基因组型,该基因组型全部对阿米卡星和头孢吡肟敏感,对左旋氧氟沙星和美洛培南耐药;PFGE基因组型H、P菌株对6种以上抗生素耐药;PFGE基因组型I和J菌株对所测9种抗生素均敏感.结论 4种稀有位点核酸内切酶结合的PFGE基因组分型可以作为临床多重耐药铜绿假单胞菌监控和鉴定的有效手段.
目的 對比分析外科重癥鑑護室多重耐藥銅綠假單胞菌的基因組差異,探索其與多重耐藥性的關繫.方法 瓊脂稀釋法檢測49株銅綠假單胞菌對臨床常用9種抗菌藥物的敏感性,應用4種稀有位點覈痠內切酶結閤的脈遲場凝膠電泳技術(PFGE)對臨床分離的株銅綠假單胞菌進行基因組分型.結果 多重耐藥銅綠假單胞菌菌株佔外科重癥鑑護室銅綠假單胞菌臨床分離株的85.7%;PFGE基因組型A菌株佔全部銅綠假單胞菌分離株的61.2%,為主導基因組型,該基因組型全部對阿米卡星和頭孢吡肟敏感,對左鏇氧氟沙星和美洛培南耐藥;PFGE基因組型H、P菌株對6種以上抗生素耐藥;PFGE基因組型I和J菌株對所測9種抗生素均敏感.結論 4種稀有位點覈痠內切酶結閤的PFGE基因組分型可以作為臨床多重耐藥銅綠假單胞菌鑑控和鑒定的有效手段.
목적 대비분석외과중증감호실다중내약동록가단포균적기인조차이,탐색기여다중내약성적관계.방법 경지희석법검측49주동록가단포균대림상상용9충항균약물적민감성,응용4충희유위점핵산내절매결합적맥충장응효전영기술(PFGE)대림상분리적주동록가단포균진행기인조분형.결과 다중내약동록가단포균균주점외과중증감호실동록가단포균림상분리주적85.7%;PFGE기인조형A균주점전부동록가단포균분리주적61.2%,위주도기인조형,해기인조형전부대아미잡성화두포필우민감,대좌선양불사성화미락배남내약;PFGE기인조형H、P균주대6충이상항생소내약;PFGE기인조형I화J균주대소측9충항생소균민감.결론 4충희유위점핵산내절매결합적PFGE기인조분형가이작위림상다중내약동록가단포균감공화감정적유효수단.
Objective To investigate the genetic differences and their relativity with multi-drug resistance of Pseudomonas aeruginosa isolated.Methods Forty-nine Pseudomonas aeruginosa isolates were characterized by antimicrobial susceptibility and four-enzyme (I-Ceu I,Spe I,Swa I,Pac I) pulsed-field gel electrophoresis (PFGE).Results 85.7% of the P.aeruginosa isolates were MDR strains.Strains with PFGE pattern A were all susceptible to amikacin and cefepime, but were resistant to levofloxacin and meropenem.Strains with PFGE Patterns H and P had resistance to 6-8 different kinds of antibiotics.Strains with PFGE Patterns I and J were susceptible to all antibiotics tested in this study.Strains with other PFGE Patterns had intermediate resistance.PFGE pattern A was the dominant pattern, which accounted for 61.2% of all P.aeruginosa strains, 100 % (2/2) in 2001, 65% (13/20) in 2002, 44.4% (8/18) in 2003 and 77.8% (7/9) in 2004.Conclusion Four-enzyme combined PFGE analysis is highly discriminatory for the subtyping of MDR P.aeruginosa isolates.