Oskoui M, Farrokh P
Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran.
Iran J Microbiol. 2010 Mar;2(1):14-21.
Infection with vancomycin-resistant enterococci (VRE) has caused a therapeutic problem. VanA and VanB resistant types are the predominant phenotypes among vancomycin resistant enetrococci. Transposon 1546 (Tn1546) harboring the vanA gene cluster, plays an important role in the horizontal transfer of vanA gene. In this study, we examined the phenotypic and genotypic diversity of a number of clinical VRE.
Twenty-four clinical VRE isolated from two university hospitals in Tehran were examined based on their antimicrobial susceptibility, Tn1546 related element organization and pulsed-field gel electrophoresis (PFGE) patterns. Integration of well-studied insertion sequence elements IS1216V, IS1542 and IS1251 was examined by PCR mapping and sequencing.
From 24 isolates, 15 isolates with VanA phenotype and 9 isolates with VanB phenotype were identified which both groups interestingly possessed the vanA gene. According to PCR mapping, our isolates were assigned to 6 main groups. In 14 (58.3%) isolates, IS1216V was inserted in vanX-vanY region and/or in truncated left-hand of Tn1546-like elements. In 11 (45.8%) isolates, both IS1216V and IS1542 were inserted in vanX-vanY and orf2-vanR regions, respectively and none of them harbored IS1251. Interestingly, PFGE of the isolates showed a high degree of diversity.
PCR mapping revealed that VanA elements in our isolates were highly heterogeneous. Overall, we found no correlation between transposon type and PFGE pattern. Genetic diversity of VRE provides practical information for epidemiological studies and our data showed horizontal transfer of VRE in this region.
耐万古霉素肠球菌(VRE)感染引发了治疗难题。VanA和VanB耐药类型是耐万古霉素肠球菌中的主要表型。携带vanA基因簇的转座子1546(Tn1546)在vanA基因的水平转移中起重要作用。在本研究中,我们检测了一些临床VRE的表型和基因型多样性。
从德黑兰的两家大学医院分离出24株临床VRE,根据其药敏性、Tn1546相关元件组织和脉冲场凝胶电泳(PFGE)图谱进行检测。通过PCR定位和测序检测深入研究的插入序列元件IS1216V、IS1542和IS1251的整合情况。
在24株分离株中,鉴定出15株VanA表型和9株VanB表型的分离株,有趣的是两组均含有vanA基因。根据PCR定位,我们的分离株被分为6个主要组。在14株(58.3%)分离株中,IS1216V插入到vanX - vanY区域和/或Tn1546样元件的截短左手端。在11株(45.8%)分离株中,IS1216V和IS1542分别插入到vanX - vanY和orf2 - vanR区域,且均未携带IS1251。有趣的是,分离株的PFGE显示出高度的多样性。
PCR定位显示我们分离株中的VanA元件高度异质性。总体而言,我们发现转座子类型与PFGE图谱之间无相关性。VRE的遗传多样性为流行病学研究提供了实用信息,我们的数据显示该区域存在VRE的水平转移。