Re. Schifferle et al., ACTIVATION OF SERUM COMPLEMENT BY POLYSACCHARIDE-CONTAINING ANTIGENS OF PORPHYROMONAS-GINGIVALIS, Journal of Periodontal Research, 28(4), 1993, pp. 248-254
We previosly reported that hot aqueous phenol extraction of Porphyromo
nas gingivalis yields a preparation containing both lipopolysaccharide
(LPS) and an antigenically distinct capsular polysaccharide (PS). In
the present study, we examined the capacity of phenol-water extracts f
rom a number of strains of P. gingivalis to activate human serum compl
ement. Anticomplementary activity of extracts from two invasive and tw
o noninvasive strains of P gingivalis was assessed in a sheep erythroc
yte hemolytic assay and in an alternative pathway-selective rabbit ery
throcyte hemolytic assay. In the sheep erythrocyte assay, extracts fro
m noninvasive strains were found to exhibit greater anticomplementary
activity than extracts derived from invasive strains. A phenol-water e
xtract from invasive strain ATCC 53977 was further resolved into its L
PS and PS fractions. Whereas isolated LPS from this strain exhibited s
trong anticomplementary activity, the PS fraction was only weakly acti
ve. Phenol-water extracts from three of four strains were found to be
potent activators of the alternative pathway, with extracts from the t
wo noninvasive strains being most active. The extract from the remaini
ng strain (ATCC 53977) was a poor activator of the alternative pathway
. Further analysis of this extract revealed, however, that the LPS fra
ction was a potent activator of the alternative pathway, although the
PS fraction exhibited negligible activity. The results of this study i
ndicate that phenol-water extracts of invasive and noninvasive strains
of P gingivalis differ in their respective anticomplementary activiti
es, with invasive strains being less active. Although extracts from bo
th invasive and noninvasive strains activated the alternative pathway,
this activity appears to be attributable to the LPS, rather than the
PS, component.