Department of Bacteriology, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Department of Medical Technology, Kansai University of Health Sciences, Kumatori, Osaka, Japan.
mSphere. 2020 Apr 8;5(2):e00102-20. doi: 10.1128/mSphere.00102-20.
Vancomycin-resistant enterococci pose a threat in the clinical setting and have been linked to hospital outbreaks worldwide. In 2017, a local spread of VanA-type vancomycin-resistant enterococci (VRE) occurred in Japan, and 25 enterococcal isolates, including 14 , 8 , and 3 isolates, were identified from four inpatients. Molecular analysis of the multispecies of VanA-type VRE revealed the involvement of both the dissemination of clonally related VRE strains between patients and the horizontal transfer of plasmids harboring the gene cluster between spp. Pulsed-field gel electrophoresis showed that the plasmid DNAs without S1 nuclease treatment were able to migrate into the gel, suggesting that the topology of the plasmid was linear. Whole-genome sequencing revealed that this plasmid, designated pELF2, was 108,102 bp long and encoded multiple antimicrobial resistance genes, including and (9). The amino acid sequences of putative replication- and transfer-related genes were highly conserved between pELF2 and pELF1, the latter of which was the first identified enterococcal conjugative linear plasmid. On comparing the genomic structure, pELF2 showed the presence of a backbone similar to that of pELF1, especially with respect to the nucleotide sequences of both terminal ends, indicating a hybrid-type linear plasmid, possessing two different terminal structures. pELF2 possessed a broad host range and high conjugation frequencies for enterococci. The easy transfer of pELF2 to different spp. might explain this local spread of multiple species, highlighting the clinical threat from the spread of antimicrobial resistance by an enterococcal linear plasmid. Increasing multidrug resistance, including vancomycin resistance, in enterococci is a major concern in clinical settings. Horizontal gene transfer, such as via plasmids, has been shown to play a crucial role in the acquisition of vancomycin resistance. Among vancomycin resistance types, the VanA type is one of the most prevalent, and outbreaks caused by VanA-type vancomycin-resistant enterococci (VRE) have occurred worldwide. Here, we describe an enterococcal linear plasmid responsible for multispecies local spread of VanA-type VRE. Such a study is important because although hospital outbreaks caused by mixed enterococcal species have been reported, this particular spread indicates plasmid transfer across species. This is a crucial finding because the high risk for such a spread of antimicrobial resistance calls for regular monitoring and surveillance.
耐万古霉素肠球菌在临床环境中构成威胁,并与全球范围内的医院爆发有关。2017 年,日本发生了 VanA 型耐万古霉素肠球菌(VRE)的局部传播,从 4 名住院患者中分离出了 25 株肠球菌分离株,包括 14 株、8 株和 3 株。对 VanA 型 VRE 的多菌种分子分析表明,患者间克隆相关 VRE 菌株的传播以及携带 基因簇的质粒在 spp. 之间的水平转移均参与其中。脉冲场凝胶电泳显示,未经 S1 核酸酶处理的质粒 DNA 能够迁移到凝胶中,表明质粒的拓扑结构为线性。全基因组测序表明,该质粒命名为 pELF2,长 108102bp,编码多种抗微生物药物耐药基因,包括 和 (9)。复制和转移相关基因的氨基酸序列在 pELF2 和 pELF1 之间高度保守,后者是第一个鉴定出的肠球菌接合性线性质粒。比较基因组结构后,pELF2 显示出与 pELF1 相似的骨架,尤其是在两个末端的核苷酸序列方面,表明其为具有两种不同末端结构的混合型线性质粒。pELF2 对肠球菌具有广泛的宿主范围和高的接合频率。pELF2 易于向不同的 spp. 转移,这可能解释了多种物种的局部传播,突出了肠球菌线性质粒传播抗微生物药物耐药性的临床威胁。临床环境中肠球菌的多药耐药性(包括万古霉素耐药性)不断增加是一个主要关注点。质粒等水平基因转移已被证明在万古霉素耐药性的获得中发挥关键作用。在万古霉素耐药类型中,VanA 型是最常见的类型之一,并且全球范围内都发生过由 VanA 型耐万古霉素肠球菌(VRE)引起的爆发。在这里,我们描述了一种肠球菌线性质粒,该质粒可导致 VanA 型 VRE 的多物种局部传播。这样的研究很重要,因为尽管已经报道了由混合肠球菌物种引起的医院爆发,但这种特殊的传播表明质粒在物种间转移。这是一个重要的发现,因为这种抗微生物药物耐药性的高风险需要进行定期监测和监测。