中国感染控制杂志
中國感染控製雜誌
중국감염공제잡지
CHINESE JOURNAL OF INFECTION CONTROL
2015年
3期
145-148
,共4页
赵亚楠%郭育奇%黄红兰%武晓琳%韦珍%孙超%赵春燕
趙亞楠%郭育奇%黃紅蘭%武曉琳%韋珍%孫超%趙春燕
조아남%곽육기%황홍란%무효림%위진%손초%조춘연
革兰阴性菌%金属β-内酰胺酶基因%IMP%VIM%多重耐药性%抗药性,微生物%医院感染
革蘭陰性菌%金屬β-內酰胺酶基因%IMP%VIM%多重耐藥性%抗藥性,微生物%醫院感染
혁란음성균%금속β-내선알매기인%IMP%VIM%다중내약성%항약성,미생물%의원감염
gram-negative bacteria%metallo-β-lactamase gene%IMP%VIM%multidrug resistance%drug resistance,microbial%healthcare-associated infection
目的:了解临床分离革兰阴性菌产 IMP 及VIM 金属β-内酰胺酶(MβLs)基因的检出情况,以及对β-内酰胺类抗生素的耐药状况。方法采用 K-B 法对临床分离的113株细菌进行药物敏感试验,采用聚合酶链反应(PCR)检测耐药基因 IMP 和 VIM ,测序并进行 BLAST 比对分析。结果1株荧光假单胞菌检出 VIM 基因;15株菌中检出 IMP 基因,其中肺炎克雷伯菌6株,鲍曼不动杆菌 3株,大肠埃希菌2株,罗尔斯顿菌、铜绿假单胞菌、无丙二酸柠檬酸杆菌、阴沟肠杆菌各1株。BLAST 结果显示,VIM 基因为VIM-2型,与基因库中序列相似度99%;IMP 基因均为 IMP-1亚型,相似度在98%~99%,高度同源。IMP 阳性菌株对头孢曲松、头孢噻肟、头孢西丁、氨曲南和亚胺培南的耐药率高于阴性菌株,差异均具有统计学意义(均 P <0.05)。结论不同菌株 IMP 基因高度同源,均为 IMP-1型,表明 IMP 基因的传播能力很强,可以突破种属的限制在不同细菌中传播。IMP 基因与细菌对β-内酰胺类抗生素耐药相关。
目的:瞭解臨床分離革蘭陰性菌產 IMP 及VIM 金屬β-內酰胺酶(MβLs)基因的檢齣情況,以及對β-內酰胺類抗生素的耐藥狀況。方法採用 K-B 法對臨床分離的113株細菌進行藥物敏感試驗,採用聚閤酶鏈反應(PCR)檢測耐藥基因 IMP 和 VIM ,測序併進行 BLAST 比對分析。結果1株熒光假單胞菌檢齣 VIM 基因;15株菌中檢齣 IMP 基因,其中肺炎剋雷伯菌6株,鮑曼不動桿菌 3株,大腸埃希菌2株,囉爾斯頓菌、銅綠假單胞菌、無丙二痠檸檬痠桿菌、陰溝腸桿菌各1株。BLAST 結果顯示,VIM 基因為VIM-2型,與基因庫中序列相似度99%;IMP 基因均為 IMP-1亞型,相似度在98%~99%,高度同源。IMP 暘性菌株對頭孢麯鬆、頭孢噻肟、頭孢西丁、氨麯南和亞胺培南的耐藥率高于陰性菌株,差異均具有統計學意義(均 P <0.05)。結論不同菌株 IMP 基因高度同源,均為 IMP-1型,錶明 IMP 基因的傳播能力很彊,可以突破種屬的限製在不同細菌中傳播。IMP 基因與細菌對β-內酰胺類抗生素耐藥相關。
목적:료해림상분리혁란음성균산 IMP 급VIM 금속β-내선알매(MβLs)기인적검출정황,이급대β-내선알류항생소적내약상황。방법채용 K-B 법대림상분리적113주세균진행약물민감시험,채용취합매련반응(PCR)검측내약기인 IMP 화 VIM ,측서병진행 BLAST 비대분석。결과1주형광가단포균검출 VIM 기인;15주균중검출 IMP 기인,기중폐염극뢰백균6주,포만불동간균 3주,대장애희균2주,라이사돈균、동록가단포균、무병이산저몽산간균、음구장간균각1주。BLAST 결과현시,VIM 기인위VIM-2형,여기인고중서렬상사도99%;IMP 기인균위 IMP-1아형,상사도재98%~99%,고도동원。IMP 양성균주대두포곡송、두포새우、두포서정、안곡남화아알배남적내약솔고우음성균주,차이균구유통계학의의(균 P <0.05)。결론불동균주 IMP 기인고도동원,균위 IMP-1형,표명 IMP 기인적전파능력흔강,가이돌파충속적한제재불동세균중전파。IMP 기인여세균대β-내선알류항생소내약상관。
Objective To investigate the detection of IMP andVIM metallo-β-lactamases (MβLs)genes in clinically iso-lated gram-negative bacteria as well as bacterial resistance toβ-lactam antimicrobial agents.Methods 113 clinically isolated bacteria were performed antimicrobial susceptibility testing by Kirby-Bauer method ,drug-resistant genes IMP and VIM were detected by polymerase chain reaction (PCR),PCR products were sequenced and aligned with BLAST software. Results VIM gene was detected in 1 Pseudomonas fluorescens strain ,IMP gene was detected in 15 strains ,they were Klebsiella pneumoniae (n=6),Acinetobacter baumannii (n=3),Escherichia coli (n=2),Ralstonia picket-tii (n=1),Pseudomonas aeruginosa (n=1 ),Citrobacter amalonaticua (n=1 ),and Enterobacter cloacae (n=1 ). BLAST results showed that VIM gene was VIM-2 subtype,similarity with gene bank was 99%;all IMP genes were IMP-1 subtype,which were highly homologous ,similarity was 98%-99%.Resistant rates of IMP positive strains to ceftriaxone,cefotaxime,cefoxitin,aztreonam and imipenem were all significantly higher than negative strains (all P <0.05).Conclusion IMP genes of different strains are highly homologous,all are IMP-1 type,indi-cating that IMP genes are highly transmissible and can spread among different species of bacteria.IMP genes are related with resistance ofβ-lactam antimicrobial agents.