Institute of Hygiene, University Hospital Münster, 48149, Münster, Germany.
Institute for Hygiene and Microbiology, University of Würzburg, 97080, Würzburg, Germany.
Sci Rep. 2024 Jan 22;14(1):1895. doi: 10.1038/s41598-024-52310-1.
Clonal transmission and horizontal gene transfer (HGT) contribute to the spread of vancomycin-resistant enterococci (VRE) in global healthcare. Our study investigated vesiduction, a HGT mechanism via membrane vesicles (MVs), for vanA and vanB genes that determine vancomycin resistance. We isolated MVs for VRE of different sequence types (STs) and analysed them by nanoparticle tracking analysis. Selected MV samples were subjected to DNA sequence analysis. In resistance transfer experiments, vancomycin-susceptible enterococci were exposed to MVs and bacterial supernatants of VRE. Compared to bacteria grown in lysogeny broth (MVs/LB), cultivation under vancomycin stress (MVs/VAN) resulted in increased particle concentrations of up to 139-fold (ST80). As a key finding, we could show that VRE isolates of ST80 and ST117 produced remarkably more vesicles at subinhibitory antibiotic concentrations (approx. 9.2 × 10 particles/ml for ST80 and 2.4 × 10 particles/ml for ST117) than enterococci of other STs (range between 1.8 × 10 and 5.3 × 10 particles/ml). In those MV samples, the respective resistance genes vanA and vanB were completely verifiable using sequence analysis. Nevertheless, no vancomycin resistance transfer via MVs to vancomycin-susceptible Enterococcus faecium was phenotypically detectable. However, our results outline the potential of future research on ST-specific MV properties, promising new insights into VRE mechanisms.
克隆传播和水平基因转移 (HGT) 导致万古霉素耐药肠球菌 (VRE) 在全球医疗保健中传播。我们的研究调查了通过膜囊泡 (MVs) 进行 HGT 的机制,以确定万古霉素耐药性的 vanA 和 vanB 基因。我们分离了不同序列类型 (ST) 的 VRE 的 MVs,并通过纳米颗粒跟踪分析对其进行了分析。选择的 MV 样本进行了 DNA 序列分析。在耐药性转移实验中,将万古霉素敏感的肠球菌暴露于 VRE 的 MV 和细菌上清液中。与在溶菌肉汤中生长的细菌 (MVs/LB) 相比,在万古霉素应激下培养 (MVs/VAN) 导致颗粒浓度增加了高达 139 倍(ST80)。作为一个关键发现,我们能够表明 ST80 和 ST117 的 VRE 分离株在亚抑菌抗生素浓度下产生的囊泡数量明显更多(对于 ST80 约为 9.2×10 个/毫升,对于 ST117 为 2.4×10 个/毫升)比其他 ST 的肠球菌(范围在 1.8×10 和 5.3×10 个/毫升之间)。在这些 MV 样本中,使用序列分析完全可以验证各自的耐药基因 vanA 和 vanB。然而,通过 MVs 向万古霉素敏感的粪肠球菌转移万古霉素耐药性在表型上是不可检测的。然而,我们的结果概述了针对特定 ST 的 MV 特性进行未来研究的潜力,有望为 VRE 机制提供新的见解。