S. Salloway et al., MILLER-FISHER SYNDROME-ASSOCIATED WITH CAMPYLOBACTER-JEJUNI BEARING LIPOPOLYSACCHARIDE MOLECULES THAT MIMIC HUMAN GANGLIOSIDE GD(3), Infection and immunity, 64(8), 1996, pp. 2945-2949
A Campylobacter jejuni strain of serotype O:10 was isolated from a pat
ient who had Miller-Fisher syndrome. In its biochemical reactions and
cellular morphology, the isolate was characteristic of typical C. jeju
ni. Antibodies against extracted lipopolysaccharide (LPS) were detecte
d by passive hemagglutination in the acute- and convalescent-phase pat
ient sera. By sodium dodecyl sulfate-polyacrylamide gel electrophoresi
s and immunoblotting with the O:10 antiserum, it was demonstrated that
the strain possessed both low- and high-molecular-weight molecules. C
hemical analysis of the LPS revealed that the core oligosaccharide has
a terminal trisaccharide epitope consisting of two molecules of siali
c acid linked to galactose, a structure reflecting the terminal region
of human ganglioside GD(3). As this trisaccharide is also present in
LPS cores of serotype O:19 strains from patients with Guillain-Barre s
yndrome but not in cores of nonneuropathic C. jejuni, a possible role
for the trisaccharide in the etiology of neuropathies is indicated, an
d a difference for distinguishing neuropathic strains from nonneuropat
hic strains may be the presence of a sialyltransferase required for th
e synthesis of this trisaccharide.