中华烧伤杂志
中華燒傷雜誌
중화소상잡지
16
2008年
6期
432-436
,共5页
蒋丽媛%薛晓东%魏莲花%司小强%刘刚%周华%俞云松
蔣麗媛%薛曉東%魏蓮花%司小彊%劉剛%週華%俞雲鬆
장려원%설효동%위연화%사소강%류강%주화%유운송
烧伤%感染%鲍氏不动杆菌%抗药性%整合子类%碳青霉烯酶
燒傷%感染%鮑氏不動桿菌%抗藥性%整閤子類%碳青黴烯酶
소상%감염%포씨불동간균%항약성%정합자류%탄청매희매
Burns%Infection%Acinetobacter baumannii%Drug resistance%Integrons%Carbapenemase
目的 明确甘肃省人民医院烧伤病房多重耐药鲍氏不动杆菌的耐药性、同源性及与整合子的关系. 方法 31株多重耐药鲍氏不动杆菌分离自该院烧伤住院患者创面分泌物标本.采用琼脂稀释法测定鲍氏不动杆菌对11种抗菌药物的最低抑菌浓度(MIC);脉冲场凝胶电泳(PFGE)分析菌株的同源性:PCR扩增I、Ⅱ、Ⅲ类整合酶及整合酶阳性菌株的整合子基因盒,进行序列分析;分析亚胺培南耐药菌株的碳青霉烯酶基因型. 结果 鲍氏不动杆菌对亚胺培南、美罗培南、哌拉西林/他唑巴坦和头孢哌酮/舒巴坦的耐药率分别为45.2%、48.4%、48.4%、41.0%,对头孢他啶、头孢吡肟、环丙沙星、阿米卡星、庆大霉素、氨曲南和哌拉西林的耐药率均在80.0%以上.所有菌株PFGE分型共分为A、B、C 3型,A克隆18株、B克隆7株、C克隆6株.20株细菌整合子扩增阳性,携带有aadA1、aadA5、aacA4、aac3、aacC1、aac(6')-Ib、catB8、drfA17和drf8基因,介导对氨基糖苷类抗生素、氯霉素、甲氧苄啶的耐药.14株亚胺培南耐药的菌株均产OXA-23型碳青霉烯酶. 结论 多重耐药鲍氏不动杆菌在该院烧伤病房播散,以A克隆为主;鲍氏不动杆菌整合子主要介导对氨基糖苷类抗生素及氯霉素的耐药性,碳青霉烯类抗生素耐药鲍氏不动杆菌均产OXA-23型碳青霉烯酶.
目的 明確甘肅省人民醫院燒傷病房多重耐藥鮑氏不動桿菌的耐藥性、同源性及與整閤子的關繫. 方法 31株多重耐藥鮑氏不動桿菌分離自該院燒傷住院患者創麵分泌物標本.採用瓊脂稀釋法測定鮑氏不動桿菌對11種抗菌藥物的最低抑菌濃度(MIC);脈遲場凝膠電泳(PFGE)分析菌株的同源性:PCR擴增I、Ⅱ、Ⅲ類整閤酶及整閤酶暘性菌株的整閤子基因盒,進行序列分析;分析亞胺培南耐藥菌株的碳青黴烯酶基因型. 結果 鮑氏不動桿菌對亞胺培南、美囉培南、哌拉西林/他唑巴坦和頭孢哌酮/舒巴坦的耐藥率分彆為45.2%、48.4%、48.4%、41.0%,對頭孢他啶、頭孢吡肟、環丙沙星、阿米卡星、慶大黴素、氨麯南和哌拉西林的耐藥率均在80.0%以上.所有菌株PFGE分型共分為A、B、C 3型,A剋隆18株、B剋隆7株、C剋隆6株.20株細菌整閤子擴增暘性,攜帶有aadA1、aadA5、aacA4、aac3、aacC1、aac(6')-Ib、catB8、drfA17和drf8基因,介導對氨基糖苷類抗生素、氯黴素、甲氧芐啶的耐藥.14株亞胺培南耐藥的菌株均產OXA-23型碳青黴烯酶. 結論 多重耐藥鮑氏不動桿菌在該院燒傷病房播散,以A剋隆為主;鮑氏不動桿菌整閤子主要介導對氨基糖苷類抗生素及氯黴素的耐藥性,碳青黴烯類抗生素耐藥鮑氏不動桿菌均產OXA-23型碳青黴烯酶.
목적 명학감숙성인민의원소상병방다중내약포씨불동간균적내약성、동원성급여정합자적관계. 방법 31주다중내약포씨불동간균분리자해원소상주원환자창면분비물표본.채용경지희석법측정포씨불동간균대11충항균약물적최저억균농도(MIC);맥충장응효전영(PFGE)분석균주적동원성:PCR확증I、Ⅱ、Ⅲ류정합매급정합매양성균주적정합자기인합,진행서렬분석;분석아알배남내약균주적탄청매희매기인형. 결과 포씨불동간균대아알배남、미라배남、고랍서림/타서파탄화두포고동/서파탄적내약솔분별위45.2%、48.4%、48.4%、41.0%,대두포타정、두포필우、배병사성、아미잡성、경대매소、안곡남화고랍서림적내약솔균재80.0%이상.소유균주PFGE분형공분위A、B、C 3형,A극륭18주、B극륭7주、C극륭6주.20주세균정합자확증양성,휴대유aadA1、aadA5、aacA4、aac3、aacC1、aac(6')-Ib、catB8、drfA17화drf8기인,개도대안기당감류항생소、록매소、갑양변정적내약.14주아알배남내약적균주균산OXA-23형탄청매희매. 결론 다중내약포씨불동간균재해원소상병방파산,이A극륭위주;포씨불동간균정합자주요개도대안기당감류항생소급록매소적내약성,탄청매희류항생소내약포씨불동간균균산OXA-23형탄청매희매.
Objective To investigate the relationship among antibiotic esistance,integron,homology of multi-drug resistant Acinetobacter Baumannii isolated from burn ward. Methods hirty-one strains of multi-drug resistant Acinetobacter baumannii were isolated from samples of burn wound exudate in hospitalized patients of Gansu Province People's Hospital.The minimum inhibitory concentrations(MIC)of these strains against 11 zntibiotics was examined by agar dilution mehod.Homology of these strains was analyzed by pulse-field gel electrophoresis(PFGE).Class 1,2 and 3 integrase,integron genes and genotype of carbapenemases were amplified by PCR and verified by DNA sequencing. Results Acinetobacter baumannii were highly resistant to all antibiotics except imipenem,meropenem,cefoperazone-sulb-actam,piperacillintazobactam(antibiotic resistance rate was 45.2%.48.4%,48.4%,41.0%,respectively).All strains were classified into 3 types of clones(A,B,C clone included 18,7,6 strains respectively)based on PFGE pattern.Integrons of 20 strains of Acinetobacter Baumannii harbored aadA1,aadA5,aacA4,aac3,catB8,aacC1,aac(6')-Ib,drfA17 and drf8 gene. Conclusion Multi-drug resistance Acinetobacter baumannii (major in clone A)spread widely in burn ward of Gansu Province People's Hospital.Integrons of Acinetobacter baumannii mediated drug resistance against aminoglycoside antibiotics,chloram-phenicol.All carbapenem-resistant Acinetobacter Baumannii can produce OXA-23 carbapenemase.