Research Group of Host-Microbe Interactions, Department of Medical Biology, Faculty of Health Sciences, UiT-The Arctic University of Norway, Norway.
Research Group of Host-Microbe Interactions, Department of Medical Biology, Faculty of Health Sciences, UiT-The Arctic University of Norway, Norway; Norwegian National Advisory Unit on Detection of Antimicrobial Resistance, Department of Microbiology and Infection Control, University Hospital of North-Norway, Tromsø, Norway.
J Proteomics. 2018 Sep 15;187:28-38. doi: 10.1016/j.jprot.2018.05.017. Epub 2018 May 30.
Enterococcus faecium is a commensal but also a bacteremia causing pathogen, which is inherently resistant to several antimicrobials and has a great ability to acquire new traits. Bacterial membrane vesicles (MVs) are increasingly recognized as a mode of cell-free communication and a way to deliver virulence factors and/or antimicrobial resistance determinants. These features make MVs interesting research targets in research on critical hospital pathogens. This study describes for the first time that E. faecium strains produce MVs. It presents a morphological as well as a proteomic analysis of MVs isolated from four different, clinically relevant E. faecium strains grown under two different conditions and identifies MV-associated proteins in all of them. Interestingly, 11 virulence factors are found among the MV-associated proteins, including biofilm-promoting proteins and extracellular matrix-binding proteins, which may aid in enterococcal colonization. Additionally, 11 antimicrobial resistance-related proteins were MV-associated. Among those, all proteins encoded by the vanA-cluster of a vancomycin resistant strain were found to be MV-associated. This implies that E. faecium MVs may be utilized by the bacterium to release proteins promoting virulence, pathogenicity and antimicrobial resistance.
Enterococcal infections, especially bacteremia and endocarditis, are challenging to treat because E. faecium have acquired resistance to multiple classes of antimicrobials, including ampicillin, aminoglycosides, and glycopeptides. Thus, research on different modes of enterococcal pathogenicity is warranted. This study utilized a proteomic approach to identify MV-associated proteins of different nosocomial E. faecium strains representing four clinically relevant sequence types (STs), namely ST17, ST18, ST78, and ST192. The presented data suggest that E. faecium MVs are involved in virulence and antimicrobial resistance.
屎肠球菌是一种共生菌,但也是一种引起菌血症的病原体,它天生对几种抗生素具有耐药性,并且具有获取新特性的巨大能力。细菌膜泡(MVs)越来越被认为是一种细胞外通讯方式,也是传递毒力因子和/或抗生素耐药决定因素的一种方式。这些特性使 MVs 成为研究重要医院病原体的研究目标。本研究首次描述了屎肠球菌菌株产生 MVs。它对从四种不同的、临床相关的屎肠球菌菌株中分离出的 MVs 进行了形态和蛋白质组学分析,并在所有菌株中鉴定了 MV 相关蛋白。有趣的是,在 MV 相关蛋白中发现了 11 种毒力因子,包括促进生物膜形成的蛋白和细胞外基质结合蛋白,这可能有助于肠球菌定植。此外,11 种与抗生素耐药相关的蛋白与 MV 相关。其中,万古霉素耐药株的 vanA 簇编码的所有蛋白都被发现与 MV 相关。这意味着屎肠球菌 MVs 可能被细菌用来释放促进毒力、致病性和抗生素耐药性的蛋白。
肠球菌感染,尤其是菌血症和心内膜炎,治疗起来具有挑战性,因为屎肠球菌已经获得了对包括氨苄西林、氨基糖苷类和糖肽类在内的多种抗生素类别的耐药性。因此,有必要研究不同的肠球菌致病性模式。本研究利用蛋白质组学方法鉴定了不同医院来源的屎肠球菌菌株的 MV 相关蛋白,这些菌株代表了四个临床相关的序列型(ST),即 ST17、ST18、ST78 和 ST192。所呈现的数据表明,屎肠球菌 MVs 参与了毒力和抗生素耐药性。