Lipopolysaccharides (LPS) were extracted from whole cells of seven strains of Bactevoides gingiudis -381, ATCC 33277, BH18/10,OMZ314,OMZ409,6/26 and HW24D-1-by the phenollwater procedure, and purified by treatment with nuclease and by repeated ultracentrifugation. These LPS were composed of hexoses, hexosamines, fatty acids, phosphorus and phosphorylated 2-keto-3-deoxyoctonate (KDO). The major components of the lipid portion of these LPS were hexadecanoic, 3-hydroxyhexadecanoic, branched 3-hydroxypentadecanoic and branched 3-hydroxyheptadecanoic acids. All the LPS preparations induced marked mitogenic and in vitro polyclonal B cell activation responses in spleen cells from both C3H/HeN and C3H/HeJ mice, exhibited no definitive preparatory activity in the local Shwartzman reaction in rabbits, but were active in the chromogenic Limulus amoebocyte lysate test. A monoclonal antibody (mAb) raised against the LPS from B. gingiudis strain 6/26 reacted with LPS from all other B. gingiudis strains tested. Other mAbs raised against LPS from B. gingiuds strains 381 and 6/26 reacted with the LPS from strains 381, ATCC 33277, BH18/10 and 6/26 (these strains were termed LPS serogroup I), as revealed by ELISA and immunodiffusion. The LPS from these strains except for 6/26 showed almost indentical patterns in SDS-PAGE stained with ammoniacal silver. A mAb raised against the LPS from B. gingivdis HW24D-1 reacted with the LPS from strains OMZ314, HW24D-1 and O M W (LPS serogroup 11). These LPS, except OMZ409, exhibited very similar profiles in SDS-PAGE. These results indicate that there are at least two Merent antigenic groups present among LPS from B. gingiudis strains, as well as a common, species-specific antigen.