首页> 外文期刊>Iranian Journal of Microbiology >Molecular analysis and antimicrobial resistance pattern of distinct strains of Pseudomonas aeruginosa isolated from cystic fibrosis patients in Iran
【24h】

Molecular analysis and antimicrobial resistance pattern of distinct strains of Pseudomonas aeruginosa isolated from cystic fibrosis patients in Iran

机译:伊朗囊性纤维化患者分离的铜绿假单胞菌不同菌株的分子分析和抗药性模式

获取原文
           

摘要

Background and Objectives: Colonization of Pseudomonas aeruginosa in Cystic Fibrosis (CF) patients may lead to severe pulmonary disease and death. Different characteristics of P. aeruginosa from these patients were determined in the present study. Materials and Methods: Antimicrobial susceptibility and AmpC-overproduction were determined. The β-lactamase genes were detected by PCR and the oprD gene was sequenced in some of the carbapenem resistance isolates. Distribution of exo genes was determined by PCR. Cytotoxicity of Exo effector proteins was measured using A549 cells. Biofilm production was determined by microtiter plate assay. Random amplified polymorphic DNA (RAPD) –PCR was performed for molecular analysis. Results: Polymyxin B, piperacillin/tazobactam and meropenem were the most active antibiotics and 9.6% of isolates were ampC overproducers. The prevalence of blaVEB, blaOXA, blaVIM, and blaPER genes were as follow: 22.7%, 3.75%, 6.25% and 3.75%, respectively. A high proportion (83.5%) of isolates was able to produce biofilm. The exoT gene was present in all isolates while exoU was present in about 35% of them. RAPD-PCR revealed 49 patterns among 78 tested isolates in which 34 patterns were detected once. Conclusion: Biofilm formation ability and relatively high frequency of exoS may contribute to the persistence of bacteria within lungs of CF patients. Some characteristics of isolates recovered from a single patient after several sampling procedures were similar, while others lacked resemblance.
机译:背景与目的:囊性纤维化(CF)患者中的铜绿假单胞菌定植可能导致严重的肺部疾病和死亡。在本研究中确定了来自这些患者的铜绿假单胞菌的不同特征。材料和方法:测定抗菌药的敏感性和AmpC的过量生产。通过PCR检测β-内酰胺酶基因,并在一些碳青霉烯抗性分离株中对oprD基因进行测序。外显子基因的分布通过PCR确定。使用A549细胞测量Exo效应蛋白的细胞毒性。通过微量滴定板测定法确定生物膜产量。进行了随机扩增多态性DNA(RAPD)–PCR的分子分析。结果:多粘菌素B,哌拉西林/他唑巴坦和美罗培南是最活跃的抗生素,而分离株的9.6%是ampC过量生产的。 blaVEB,blaOXA,blaVIM和blaPER基因的患病率分别为:22.7%,3.75%,6.25%和3.75%。高比例(83.5%)的分离株能够产生生物膜。 exoT基因存在于所有分离株中,而exoU则存在于其中约35%。 RAPD-PCR揭示了78种测试菌株中的49种模式,其中一次检测到34种模式。结论:生物膜形成能力和较高的exoS频率可能有助于CF患者肺部细菌的持久性。经过几次采样程序从单个患者中回收的分离株的某些特征相似,而另一些则缺乏相似性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号