检验医学 ›› 2012, Vol. 27 ›› Issue (9): 749-753.

• 微生物学检验论著 • 上一篇    下一篇

耐碳青霉烯类鲍曼不动杆菌6种基因及ISAbal插入序列的研究

廖晚珍   

  1. 1. 南昌大学第一附属医院检验科,江西 南昌 330006;2. 南昌大学第一附属医院呼吸科,江西 南昌 330006
  • 收稿日期:2012-07-03 修回日期:2012-08-31 出版日期:2012-09-12 发布日期:2012-09-12
  • 通讯作者: 廖晚珍
  • 作者简介:廖晚珍,男,1952年生,副主任技师,主要从事临床细菌学与真菌学、分子生物学研究。

Research on six genes and insertion sequence ISAbal of carbopenems-resistant Acinetobacter baumannii

  1. 1. Department of Clinical Laboratory,the First Affiliated Hospital of Nanchang University,Jiangxi Nanchang 330006,China; 2. Department of Respiration,the First Affiliated Hospital of Nanchang University,Jiangxi Nanchang 330006,China
  • Received:2012-07-03 Revised:2012-08-31 Online:2012-09-12 Published:2012-09-12

摘要: 目的 研究耐碳青霉烯类鲍曼不动杆菌(CRAB)的基因型特点和与插入序列ISAbal的关系,探讨其耐药机制。方法 收集CRAB 70株(非重复)和碳青霉烯类敏感鲍曼不动杆菌10株,采用2-巯基丙酸抑制试验检测金属β-内酰胺酶(MBLs);采用多重聚合酶链反应(PCR)扩增blaIMP、blaVIM、blaOXA-23、blaOXA-24、blaOXA-51、blaOXA-58、ISAbalOXA-23,扩增产物DNA测序进行比对。结果 70株CRAB 2-巯基丙酸与头孢他啶协同试验全部为阴性(即MBLs阴性),用7对特异性引物对70株CRAB和10株敏感菌进行PCR扩增,所有CRAB均携带blaOXA-23、blaOXA-51,未检出blaOXA-24;1株含有blaOXA-58;80株均不携带blaIMP和blaVIM;插入序列ISAbalOXA-23 70株CRAB均有表达,敏感菌均不表达。结论 CRAB的主要耐药基因是blaOXA-51和blaOXA-23;另外,blaOXA-23上游都存在插入序列ISAbal。鲍曼不动杆菌的耐药性与MBLs、blaOXA-24、blaOXA-58无相关性。

关键词:

mso-ascii-theme-font: minor-latin, mso-fareast-theme-font: minor-fareast, mso-hansi-theme-font: minor-latin, mso-fareast-font-family: 宋体, mso-ascii-font-family: Calibri, mso-hansi-font-family: Calibri">鲍曼不动杆菌font-size: 7.5pt" lang="EN-US">, mso-ascii-theme-font: minor-latin, mso-fareast-theme-font: minor-fareast, mso-hansi-theme-font: minor-latin, mso-fareast-font-family: 宋体, mso-ascii-font-family: Calibri, mso-hansi-font-family: Calibri">金属酶font-size: 7.5pt" lang="EN-US">, mso-ascii-theme-font: minor-latin, mso-fareast-theme-font: minor-fareast, mso-hansi-theme-font: minor-latin, mso-fareast-font-family: 宋体, mso-ascii-font-family: Calibri, mso-hansi-font-family: Calibri">碳青霉烯酶font-size: 7.5pt" lang="EN-US">, mso-ascii-theme-font: minor-latin, mso-fareast-theme-font: minor-fareast, mso-hansi-theme-font: minor-latin, mso-fareast-font-family: 宋体, mso-ascii-font-family: Calibri, mso-hansi-font-family: Calibri">基因型font-size: 7.5pt" lang="EN-US">, mso-ascii-theme-font: minor-latin, mso-fareast-theme-font: minor-fareast, mso-hansi-theme-font: minor-latin, mso-fareast-font-family: 宋体, mso-ascii-font-family: Calibri, mso-hansi-font-family: Calibri">插入序列ISAbal

Abstract: Objective To study the relationship between the genotype characteristics and insertion sequence ISAbal of carbopenems-resistant Acinetobacter baumannii(CRAB),and investigate the drug-resistant mechanism.  Methods A total of 70 strains of CRAB (no repeat strains) and 10 strains of carbopenems-sensitive Acinetobacter baumannii were collected. Metalloenzyme beta-lactamase (MBLs) were detected by 2-mercaptopropionic acid inhibition test. The blaIMP,blaVIM,blaOXA-23,blaOXA-24,blaOXA-51,blaOXA-58 and ISAbalOXA-23 were amplified by multiplex polymerase chain reaction (PCR). The amplified products were measured for DNA sequence.  Results The synergy tests were negative (MBLs negative) by 2-mercaptopropionic acid and ceftazime in 70 strains of CRAB. Through 7 pairs of specific primers,70 strains of CRAB and 10 strains of carbopenems-sensitive Acinetobacter baumannii were determined for PCR amplification. All the CRAB strains carried blaOXA-23 and blaOXA-51,but blaOXA-24 was never detected. Only 1 strain carried blaOXA-58,and the 80 strains did not carry blaIMP and blaVIM. In addition,all the CRAB strains carried insertion sequence ISAbalOXA-23,however,all the sensitive strains did not carry.  Conclusions Major genes are blaOXA-51 and blaOXA-23 in the CRAB strains. Insertion sequence ISAbal is located in the upstream of blaOXA-23. There is no correlation among drug-resistance of Acinetobacter baumannii to MBLs,blaOXA-24 and blaOXA-58.

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