中华流行病学杂志
中華流行病學雜誌
중화류행병학잡지
CHINESE JOURNAL OF EPIDEMIOLOGY
2009年
8期
832-835
,共4页
曹敬荣%魏星%闫中强%沈定霞%罗燕萍
曹敬榮%魏星%閆中彊%瀋定霞%囉燕萍
조경영%위성%염중강%침정하%라연평
鲍曼不动杆菌%多重耐药%分子流行病学
鮑曼不動桿菌%多重耐藥%分子流行病學
포만불동간균%다중내약%분자류행병학
Acinetobacter baumannii%Multidrug-resistant%Epidemiology,molecular
目的 研究不同医院分离的鲍曼不动杆菌产碳青霉烯酶的基因型和分子流行特征.方法 采用琼脂稀释法检测64株多重耐药鲍曼不动杆菌对抗菌药物的最小抑菌浓度(MIC);PCR检测碳青霉烯酶基因、整合酶基因及per基因,选取不同的耐药克隆菌株进行序列测定;脉冲场凝胶电泳(PFGE)分析菌株同源关系,确定菌株的分子流行特征.结果 50株菌(78.1%)携带blaOXA-23-like基因,经测序分析确定为OXA-23;1株菌检测出blaOXA-58-like基因;57株菌(89.1%)携带I类整合子;25株菌(39.1%)检测出blaPER-1基因.PFGE图谱显示64株菌分为A、B、C、D、E等13个基因型,三家医院分别以A型、B型和U型为主要流行株.结论 三家医院均发现多耐药鲍曼不动杆菌的播散流行,不同医院间和同一医院不同科室间存在同型别流行;三家医院多耐药鲍曼不动杆菌产生的碳青霉烯酶常携带OXA-23型酶,同时检测出blaOXA-58、I类整合子和balPER基因.
目的 研究不同醫院分離的鮑曼不動桿菌產碳青黴烯酶的基因型和分子流行特徵.方法 採用瓊脂稀釋法檢測64株多重耐藥鮑曼不動桿菌對抗菌藥物的最小抑菌濃度(MIC);PCR檢測碳青黴烯酶基因、整閤酶基因及per基因,選取不同的耐藥剋隆菌株進行序列測定;脈遲場凝膠電泳(PFGE)分析菌株同源關繫,確定菌株的分子流行特徵.結果 50株菌(78.1%)攜帶blaOXA-23-like基因,經測序分析確定為OXA-23;1株菌檢測齣blaOXA-58-like基因;57株菌(89.1%)攜帶I類整閤子;25株菌(39.1%)檢測齣blaPER-1基因.PFGE圖譜顯示64株菌分為A、B、C、D、E等13箇基因型,三傢醫院分彆以A型、B型和U型為主要流行株.結論 三傢醫院均髮現多耐藥鮑曼不動桿菌的播散流行,不同醫院間和同一醫院不同科室間存在同型彆流行;三傢醫院多耐藥鮑曼不動桿菌產生的碳青黴烯酶常攜帶OXA-23型酶,同時檢測齣blaOXA-58、I類整閤子和balPER基因.
목적 연구불동의원분리적포만불동간균산탄청매희매적기인형화분자류행특정.방법 채용경지희석법검측64주다중내약포만불동간균대항균약물적최소억균농도(MIC);PCR검측탄청매희매기인、정합매기인급per기인,선취불동적내약극륭균주진행서렬측정;맥충장응효전영(PFGE)분석균주동원관계,학정균주적분자류행특정.결과 50주균(78.1%)휴대blaOXA-23-like기인,경측서분석학정위OXA-23;1주균검측출blaOXA-58-like기인;57주균(89.1%)휴대I류정합자;25주균(39.1%)검측출blaPER-1기인.PFGE도보현시64주균분위A、B、C、D、E등13개기인형,삼가의원분별이A형、B형화U형위주요류행주.결론 삼가의원균발현다내약포만불동간균적파산류행,불동의원간화동일의원불동과실간존재동형별류행;삼가의원다내약포만불동간균산생적탄청매희매상휴대OXA-23형매,동시검측출blaOXA-58、I류정합자화balPER기인.
Objecfive To investigate antibiotic resistance,carbapenemase genotype and the molecular epidemiology of multidrug-resistant Acinetobacter baumannii (Aba) collected from 3 military hospitals in China.Methotis The minimum inhibitory concentrations (MIC) were examined by ager dilution method.Genotypes of carbapenemases were amplified by multiplex PCR and its products were sequenced.PCR was used to detect per gene,Homology of the resistant isolates was analyzed by pulse-field gel electrophoresis(PFGE).Results Among the 64 MDRA strains,78.1%(50)strains possessed blaOXA-23 gene,89.1%(57) carried Class 1 integrase gene,39.1% (25) with blaPER-1 gene,and 1 strain with blaOXA-58-like gene.PFGE showed that 13(A,B,C,D,E genotype) different clones were identified in these strains.A,B,and U clones were the predominant clones in three hospitals,respectitively.Conclusion OutbreaEs of muitidrug-rcsistant Aba occurred at 3 military hospitals with the most prevalent carbapenemase as OXA-23 enzyme.OXA-58 type of carbapenemase and per-1 in Aba were also isolated.