Bacteroides fragilis isolates from intestinal and non-intestinal infections
, normal flora and the environment were examined for properties linked with
interactions among cells in vitro. Different adhesion molecules were detec
ted in agglutination assays with human erythrocytes and tests for auto-aggl
utination and adherence to human colon carcinoma cells (HT29), There was no
correlation between these properties, indicating that independent molecule
s are involved, Treatment with trypsin, heat or EDTA inhibited agglutinatio
n and adherence, suggesting that these molecules are proteins. The lack of
correlation with the origin of the strains did not permit any of these acti
vities to be recognised as virulence markers. The expression of fragilysin,
a protease associated with damage to intestinal cells and bacterial transl
ocation, was examined, Only those strains from patients with diarrhoea expr
essed this protease activity in assays with HT29 cells and this was confirm
ed by specific PCR far the bft gene. The activity of fragilysin as an enter
otoxin was confirmed in the rabbit intestinal ligated loop assay. The assoc
iation of this property only with strains from intestinal infections indica
tes that it is too early to suggest this protease as a determinant factor o
f B. fragilis invasiveness.