fig1

Biological properties and potential pathogenic mechanisms of oral bacterial-derived extracellular vesicles in oral and systemic diseases

Figure 1. Schematic representation of bacterial membrane vesicle biogenesis and cell wall architecture. Multilayered cell wall structure comprising, from the outermost to innermost, LPS/OM, a PG layer, and an IM. The OM undergoes local evagination to form OMVs that encapsulate LPS, porins, and surface proteins; (B) Magnified view of OMV budding: Asymmetry in OM lipid composition and remodeling of lipid A drive membrane curvature and vesicle scission from the cell envelope; (C) Gram-positive cell envelope architecture consisting of a thick PG layer that directly encloses the CM, with teichoic acids and lipoteichoic acids interspersed throughout; (D) CM evagination leads to CMV formation, wherein membrane proteins and cytosolic cargo are encapsulated. These vesicles are released extracellularly via a yet-to-be-elucidated mechanism that likely traverse the thick PG layer. Note: Other vesicle subtypes (e.g., OIMVs, eOMVs, nanotubules) have been reported in bacteria but remain to be characterized in oral species; accordingly, they are not depicted in this schematic. Created in BioRender. Xumeng, D. (2026) https://BioRender.com/8w62rdx. LPS: Lipopolysaccharide; OM: outer membrane; PG: peptidoglycan; IM: inner membrane; OMVs: outer membrane vesicles; CM: cytoplasmic membrane; CMV: cytoplasmic membrane vesicle; OIMVs: outer-inner membrane vesicles; eOMVs: explosive outer membrane vesicles; PS: periplasmic space.

Extracellular Vesicles and Circulating Nucleic Acids
ISSN 2767-6641 (Online)
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