4.4 Article

Outer membrane vesicles of Tannerella forsythia: biogenesis, composition, and virulence

Journal

MOLECULAR ORAL MICROBIOLOGY
Volume 30, Issue 6, Pages 451-473

Publisher

WILEY
DOI: 10.1111/omi.12104

Keywords

atomic force microscopy; electron microscopy; inflammatory response; outer membrane vesicles; periodontal pathogen; Tannerella forsythia strain ATCC 43037 versus strain 92A2

Funding

  1. Austrian Science Fund FWF [P24317-B22]
  2. International Team of Implantology [781_2011]
  3. PhD program 'BioToP-Biomolecular Technology of Proteins' (Fund, FWF project) [W1224]
  4. Austrian Science Fund (FWF) [P24317, P24305] Funding Source: Austrian Science Fund (FWF)
  5. Austrian Science Fund (FWF) [P 24317, P 24305] Funding Source: researchfish

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Tannerella forsythia is the only red-complex' bacterium covered by an S-layer, which has been shown to affect virulence. Here, outer membrane vesicles (OMVs) enriched with putative glycoproteins are described as a new addition to the virulence repertoire of T.forsythia. Investigations of this bacterium are hampered by its fastidious growth requirements and the recently discovered mismatch of the available genome sequence (92A2=ATCC BAA-2717) and the widely used T.forsythia strain (ATCC43037). T. forsythia was grown anaerobically in serum-free medium and biogenesis of OMVs was analyzed by electron and atomic force microscopy. This revealed OMVs with a mean diameter of similar to 100nm budding off from the outer membrane while retaining the S-layer. An LC-ESI-TOF/TOF proteomic analysis of OMVs from three independent biological replicates identified 175 proteins. Of these, 14 exhibited a C-terminal outer membrane translocation signal that directs them to the cell/vesicle surface, 61 and 53 were localized to the outer membrane and periplasm, respectively, 22 were predicted to be extracellular, and 39 to originate from the cytoplasm. Eighty proteins contained the Bacteroidales O-glycosylation motif, 18 of which were confirmed as glycoproteins. Release of pro-inflammatory mediators from the human monocytic cell line U937 and periodontal ligament fibroblasts upon stimulation with OMVs followed a concentration-dependent increase that was more pronounced in the presence of soluble CD14 in conditioned media. The inflammatory response was significantly higher than that caused by whole T.forsythia cells. Our study represents the first characterization of T.forsythia OMVs, theirproteomic composition and immunogenic potential.

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