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中国临床药理学与治疗学 ›› 2014, Vol. 19 ›› Issue (10): 1093-1098.

• 基础研究 • 上一篇    下一篇

耐碳青霉烯类抗生素鲍曼不动杆菌耐药机制的研究

汪红, 胡龙华, 宁长秀, 杭亚平, 钟桥石, 胡晓彦, 章白苓, 贾坤如   

  1. 南昌大学第二附属医院检验科,南昌 330006,江西
  • 收稿日期:2014-03-07 修回日期:2014-08-07 出版日期:2014-10-26 发布日期:2014-10-29
  • 通讯作者: 胡龙华,男,主任技师,硕士生导师,研究方向:临床微生物学及细菌耐药机制。 Tel: 0791-86300410 E-mail: longhuahu@163.com
  • 作者简介:汪红,女,在读硕士研究生,研究方向:临床微生物学及细菌耐药机制。
  • 基金资助:
    江西省科技支撑计划(20112BBG70054)

Study on the mechanism of carbapenem resistance in Acinetobacter baumannii

WANG Hong, HU Long-hua, NING Chang-xiu, HANG Ya-ping, ZHONG Qiao-shi, HU Xiao-yan, ZHANG Bai-ling, JIA Kun-ru   

  1. Department of Clinical Laboratory,the Second Affiliated Hospital of Nanchang University,Nanchang 330006 , Jiangxi,China
  • Received:2014-03-07 Revised:2014-08-07 Online:2014-10-26 Published:2014-10-29

摘要: 目的 调查和研究南昌地区鲍曼不动杆菌对碳青霉烯类抗生素的耐药机制。方法 收集南昌大学第二附属医院2012年间临床分离的耐亚胺培南鲍曼不动杆菌(CRAB)非重复株。Vitek-32型全自动微生物分析仪进行菌株鉴定,K-B法进行药敏试验,三维试验检测AmpC酶,EDTA协同试验检测金属β-内酰胺酶,采用聚合酶链反应(PCR)扩增耐药基因,并对阳性产物进行双向测序分析,确定其基因型。结果 84株CRAB对临床常用的12种抗菌药物有9种耐药率>90%,对头孢哌酮-舒巴坦的耐药率最低(44.0%),所有菌株均为多重耐药株。三维试验在83株菌(98.8%)中检出AmpC酶,协同试验未检出产金属酶菌株。所有菌株均携带blaOXA-23、blaOXA-51及blaADC基因,1株携带blaOXA-58基因,未检测到blaOXA-24及金属酶基因(blaIMP、blaVIM-2、blaNDM-1及blaSIM-1); 外排泵编码基因adeB、调控基因adeS和adeR的检出率分别为 98.8%( 83/84) 、81.0%( 68/84) 和 67.9%( 57/84);所有菌株均检出外膜蛋白carO基因;69株(82.1%)检测出I类整合酶基因(intI1),全部菌株携带插入序列ISAba1。结论 南昌地区CRAB耐药性及多重耐药性非常严重,鲍曼不动杆菌对碳青霉烯类抗生素耐药的主要机制为产OXA-23型碳青霉烯酶,AmpC酶、外排泵AdeABC、I类整合子和插入序列ISAba1,可能与CRAB的多重耐药性密切相关。

关键词: 碳青霉烯类抗生素, 鲍曼不动杆菌, 耐药机制

Abstract: AIM: To investigate the mechanism of carbapenems resistance in Acinetobacter baumannii in nanchang. METHODS: Nonduplicate carbapenem- resistant A.baumannii (CRAB) isolates collected during 2012 in Second Affiliated Hospital of Nanchang University,strains were identified by vitek-32 automatic microbe analyzer, antimicrobial susceptibility testing by Kirby-Bauer method,AmpC enzyme by three dimensional test,Metallo β-lactamases(MBLs) by EDTA synergy test. Resistance genes were amplified by PCR,the positive results were sequenced to identify the genotype. RESULTS: More than 90% of 84 CRAB isolates were resistant to 9 of 12 antimicrobial agents tested,but the least resistant to cefoperazone-sulbactam(44.0%),and all the strains were multiple drug-resistant. Among the 84 isolates,AmpC enzyme in 83(98.8%) strains was detected,no MBLs-producing strain was found by synergy test. All strains had blaOXA-23, blaOXA-51 and blaADC genes and one had blaOXA-58 gene,while MBLs and blaOXA-24 genes were all negative. The positive rates of adeB,adeS and adeR genes were 98.8%(83/84), 81.0%(68/84) and 67.9%(57/84). The carO gene was found in all isolates,class I intergase gene was detected in 69 isolates,each strain carried ISAba1. CONCLUSION: The drug resistance of CRAB is very severer in nanchang. Production of OXA-23 carbapenemase in A.baumannii is major mechanism of carbapenems resistance in local area. AmpC enzyme, efflux pump AdeABC, class I integron and ISAba1 may be closely related to multidrug resistance of CRAB.

Key words: carbapenems, acinetobacter baumannii, resistance mechanism

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