K-ANTIGENS IN PORPHYROMONAS-GINGIVALIS ARE ASSOCIATED WITH VIRULENCE

Citation
Aj. Vanwinkelhoff et al., K-ANTIGENS IN PORPHYROMONAS-GINGIVALIS ARE ASSOCIATED WITH VIRULENCE, Oral microbiology and immunology, 8(5), 1993, pp. 259-265
Citations number
26
Categorie Soggetti
Immunology,Microbiology
ISSN journal
09020055
Volume
8
Issue
5
Year of publication
1993
Pages
259 - 265
Database
ISI
SICI code
0902-0055(1993)8:5<259:KIPAAW>2.0.ZU;2-G
Abstract
We investigated antigens in spreading and non-spreading Porphyromonas gingivalis strains. On the basis of differences in virulence in the mo use model, 8 strains were selected for antiserum production in rabbits . Hyperimmune sera were tested by double immunoprecipitation and immun oelectrophoresis. Besides a common antigen, differences in antigenic c omposition were observed in the thermolabile antigens between all stra ins tested. Two different heat-stable antigens were found after heatin g at 120-degrees-C. One such antigen was detected after sonication of the pellet fraction of autoclaved P. gingivalis cells. This antigen cr oss-reacted with 6 of the 8 immune sera. This somatic antigen was almo st neutrally charged and sensitive to sodium periodate treatment, sugg estive of lipopolysaccharide. A second heat-stable antigen was detecte d in the supernatant of autoclaved strains of W 83, W 50, HG 184 and A 7A1-28. These non-somatic antigens were strain-specific, i.e., no cros s-reactivity was found with heterologous hyperimmune sera. An exceptio n was strain W 50, which had a non-somatic heat-stable antigen which w as recognized by W 83 antiserum. These antigens were resistant to DNAs e, RNAse and proteinase-K treatment but were degraded by sodium period ate. In immunoelectrophoresis, these antigens appeared to be negativel y charged. These properties are characteristics of a K-antigen, which likely represent a thermostable carbohydrate capsule. The presence of K-antigen correlates very well with the serum resistance, the low chem iluminescence, the resistance to phagocytosis and the need for opsoniz ation with specific antibodies for complement-mediated killing of viru lent P gingivalis strains. We propose to designate these antigens in P gingivalis W 83 and W 50 as K1, in HG 184 as K2 and in A7A1-28 as K3.