S. Miyazaki et al., The pathogenic role of fimbriae of Haemophilus influenzae type b in murinebacteraemia and meningitis, J MED MICRO, 48(4), 1999, pp. 383-388
Complement activation and development of murine bacteraemia and meningitis
following intranasal instillation of cell-bound fimbriated or non-fimbriate
d organisms were compared to clarify the role of fimbriae in the pathogenes
is of illnesses caused by Haemophilus influenza type b (Hib). In-vitro resi
stance of non-fimbriate bacteria to the bactericidal effects of normal huma
n serum was at least 400 times greater than that of fimbriate bacteria. The
amount of C3 bound to fimbriate Hib was more than that to non-fimbriate Hi
b. When mice were infected with fimbriate bacteria, 11.5% died. When mice w
ere infected with non-fimbriate bacteria, the mean number of viable organis
ms gradually increased or was constant up to day 7; 38.5% of these mice die
d, These in vivo results were coincident with the in-vitro data. However, t
he content of polyribosyl ribitol phosphate (PRP) in fimbriate organisms wa
s the same as in non-fimbriate organisms. These results indicate that fimbr
iate Hib may be less likely to produce bacteraemia and meningitis, correlat
ing,vith the greater susceptibility to complement-mediated bacteriolysis an
d the lower mortality seen,vith this type of organism, although fimbriae in
crease adherence to epithelial cells (mucosal surface).