首页> 美国卫生研究院文献>PLoS Clinical Trials >Mobile Insertion Cassette Elements Found in Small Non-Transmissible Plasmids in Proteeae May Explain qnrD Mobilization
【2h】

Mobile Insertion Cassette Elements Found in Small Non-Transmissible Plasmids in Proteeae May Explain qnrD Mobilization

机译:在Proteeae的小型不可传播质粒中发现的移动插入盒式元件可能解释了qnrD的动员

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

qnrD is a plasmid mediated quinolone resistance gene from unknown origin, recently described in Enterobacteriaceae. It encodes a pentapeptide repeat protein 36–60% different from the other Qnr (A, B, C, S and VC). Since most qnrD-positive strains were described as strains belonging to Proteus or Providencia genera, we hypothesized that qnrD originated in Proteeae before disseminating to other enterobacterial species. We screened 317 strains of Proteeae for qnrD and its genetic support by PCR. For all the seven qnrD-positive strains (4 Proteus mirabilis, 1 Proteus vulgaris and 2 Providencia rettgeri) the gene was carried onto a small non-transmissible plasmid, contrarily to other qnr genes that are usually carried onto large multi-resistant plasmids. Nucleotide sequences of the qnrD-bearing plasmids were 96% identical. Plasmids contained 3 ORFs apart from qnrD and belonged to an undescribed incompatibility group. Only one plasmid, in P. vulgaris, was slightly different with a 1,568-bp insertion between qnrD and its promoter, leading to absence of quinolone resistance. We sought for similar plasmids in 15 reference strains of Proteeae, but which were tested negative for qnrD, and found a 48% identical plasmid (pVERM) in Providencia vermicola. In order to explain how qnrD could have been inserted into such native plasmid, we sought for gene mobilization structures. qnrD was found to be located within a mobile insertion cassette (mic) element which sequences are similar to one mic also found in pVERM. Our conclusions are that (i) the small non-transmissible qnrD-plasmids described here may result from the recombination between an as-yet-unknown progenitor of qnrD and pVERM, (ii) these plasmids are maintained in Proteeae being a qnrD reservoir (iii) the mic element may explain qnrD mobilization from non-transmissible plasmids to mobilizable or conjugative plasmids from other Enterobacteriaceae, (iv) they can recombined with larger multiresistant plasmids conjugated in Proteeae.
机译:qnrD是来自未知来源的质粒介导的喹诺酮抗性基因,最近在肠杆菌科中有描述。它编码的五肽重复蛋白与其他Qnr(A,B,C,S和VC)差异36-60%。由于大多数qnrD阳性菌株被描述为属于变形杆菌或Providencia属的菌株,因此我们假设qnrD起源于Proteeae,然后传播到其他肠细菌物种。我们通过PCR筛选了317株Proteeae的qnrD及其遗传支持。对于所有七个qnrD阳性菌株(4个奇异变形杆菌,1个寻常变形杆菌和2个瑞氏普罗维登斯氏菌),该基因被携带到一个小的不可传播质粒上,这与通常携带在大型多抗性质粒上的其他qnr基因相反。带有qnrD的质粒的核苷酸序列是96%相同的。质粒除qnrD外还包含3个ORF,属于一个未描述的不相容性组。在 P中只有一个质粒。寻常型 qnrD 及其启动子之间的插入长度为1,568-bp略有不同,导致对喹诺酮类药物没有耐药性。我们在15个 Proteeae 参比菌株中寻找相似的质粒,但对 qnrD 进行了阴性测试,并在 Providencia vermicola中发现了48%相同的质粒(pVERM)。 。为了解释如何将 qnrD 插入此类天然质粒,我们寻求基因动员结构。发现 qnrD 位于移动插入盒(mic)元件内,其序列类似于在pVERM中也发现的一种麦克风。我们的结论是(i)这里所述的小的不可传播的 qnrD 质粒可能是由于 qnrD 的迄今未知的祖细胞与pVERM重组所致,( ii)这些质粒被保存在作为 qnrD 库的 Proteeae 中(iii)mic元件可以解释 qnrD 从非传播性质粒到可动员的动员或其他肠杆菌科的结合质粒,(iv)它们可以与 Proteeae 中结合的较大的多抗性质粒重组。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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