首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Characterization of the novel optrA-carrying pseudo-compound transposon Tn7363 and an Inc18 plasmid carrying cfr(D) in Vagococcus lutrae
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Characterization of the novel optrA-carrying pseudo-compound transposon Tn7363 and an Inc18 plasmid carrying cfr(D) in Vagococcus lutrae

机译:携带optrA的新型假化合物转座子Tn7363和携带cfr(D)的Inc18质粒在Lutrae迷霉菌中的表征

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摘要

Objectives To investigate the genetic context and transferability of the oxazolidinone resistance genes cfr(D) and optrA in a porcine Vagococcus lutrae isolate. Methods V. lutrae isolate BN31 was screened for the presence of known oxazolidinone resistance genes via PCR assays. Conjugation experiments were carried out to assess horizontal transferability of resistance genes. WGS was performed using a combination of Nanopore MinION and Illumina HiSeq platforms. Detection of a translocatable unit (TU) was conducted by PCR. Results V. lutrae isolate BN31 harboured the oxazolidinone resistance genes cfr(D) and optrA. The optrA gene, together with the phenicol resistance gene fexA, was located on a novel pseudo-compound transposon, designated Tn7363. Tn7363 was bounded by two copies of the new insertion sequence ISVlu1, which represented a new member of the ISL3 family. A TU, comprising one copy of ISVlu1 and the segment between the two IS elements including the optrA gene, was detected. The cfr(D) gene and an erm(B) gene were identified on the broad-host-range Inc18 plasmid pBN31-cfrD, a pAM beta 1-like plasmid. Similar to plasmid pAM beta 1, plasmid pBN31-cfrD was conjugative. Conclusions To the best of our knowledge, we report the first identification of the cfr(D) and optrA in Vagococcus. Two novel oxazolidinone resistance gene-carrying mobile genetic elements, Tn7363 and pBN31-cfrD, were identified in V. lutrae BN31. Considering their transmission potential, attention should be paid to the risk of transfer of the optrA and cfr(D) genes from V. lutrae to clinically more important bacterial pathogens.
机译:目的 探讨猪卢氏菌分离株中噁唑烷酮抗性基因cfr(D)和optrA的遗传背景和可转移性。方法 通过PCR法筛选出的乳酸弧菌BN31中已知的恶唑烷酮抗性基因。通过偶联实验评估抗性基因的水平转移性。WGS使用Nanopore MinION和Illumina HiSeq平台的组合进行。通过PCR检测可转位单位(TU)。结果 乳草分离株BN31含有噁唑烷酮抗性基因cfr(D)和optrA。optrA 基因与苯尼考抗性基因 fexA 一起位于一种新型假化合物转座子上,命名为 Tn7363。 Tn7363 由新插入序列 ISVlu1 的两个拷贝结合,该序列代表 ISL3 家族的新成员。检测到一个 TU,包括 ISVlu1 的一个拷贝和两个 IS 元件之间的片段,包括 optrA 基因。cfr(D) 基因和 erm(B) 基因在宽宿主 Inc18 质粒 pBN31-cfrD(一种 pAM β1 样质粒)上鉴定。与质粒pAM beta 1类似,质粒pBN31-cfrD是偶联的。结论 据我们所知,我们报道了迷走球菌中cfr(D)和optrA的首次鉴定。在 V. lutrae BN31 中鉴定出两种新型的噁唑烷酮抗性基因携带可移动遗传元件 Tn7363 和 pBN31-cfrD。考虑到其传播潜力,应注意optrA和cfr(D)基因从卢特雷弧菌转移到临床上更重要的细菌病原体的风险。

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