The lactosylceramide binding specificity of Helicobacter pylori

• Published in: Glycobiology (Oxford) 1998-04, Vol.8 (4), p.297-309
• Main Authors: Ångström, Jonas, Teneberg, Susann, Milh, Maan Abul, Larsson, Thomas, Leonardsson, Iréne, Olsson, Britt-Marie, Halvarsson, Maria ölwegÅrd, Danielsson, Dan, Näslund, Ingmar, Ljungh, Åsa, Wadström, Torkel, Karlsson, Karl-Anders
• Format: Article
• Language: English
• Subjects: Animals; bacterial adhesion; Bacterial Adhesion - physiology; Binding Sites; Carbohydrate Conformation; Carbohydrate Sequence; ceramide preference; Chromatography, Thin Layer; Gastric Mucosa - metabolism; Gastric Mucosa - microbiology; Glycosphingolipids - chemistry; Glycosphingolipids - metabolism; Helicobacter pylori; Helicobacter pylori - pathogenicity; Helicobacter pylori - physiology; Humans; In Vitro Techniques; lactosylceramide; Lactosylceramides - chemistry; Lactosylceramides - metabolism; Liposomes; Mass Spectrometry; Models, Molecular; Molecular Sequence Data
• ISSN: 0959-6658; 1460-2423
• DOI: 10.1093/glycob/8.4.297

The possible role of glycosphingolipids as adhesion receptors for the human gastric pathogen Helicobacter pylori was examined by use of radiolabeled bacteria, or protein extracts from the bacterial cell surface, in the thin-layer chromatogram binding assay. Of several binding specificities found, the binding to lactosylceramide is described in detail here, the others being reported elsewhere. By autoradiography a preferential binding to lactosylceramide having sphingosine/phytosphingosine and 2-D hydroxy fatty acids was detected, whereas lactosylceramide having sphingosine and nonhydroxy fatty acids was consistently nonbinding. A selective binding of H.pylori to lactosylceramide with phytosphingosine and 2-D hydroxy fatty acid was obtained when the different lactosylceramide species were incorporated into liposomes, but only in the presence of cholesterol, suggesting that this selectivity may be present also in vivo. Importantly, lactosylceramide with sphingosine and hydroxy fatty acids does not bind in this assay. Furthermore, a lactosylceramide-based binding pattern obtained for different trisaccharide glycosphingolipids is consistent with the assumption that this selectivity is due to binding of a conformation of lactosylceramide in which the oxygen of the 2-D fatty acid hydroxyl group forms a hydrogen bond with the Glc hydroxy methyl group, yielding an epitope presentation different from other possible conformers. An alternative conformation that may come into consideration corresponds to the crystal structure found for cerebroside, in which the fatty acid hydroxyl group is free to interact directly with the adhesin. By isolating glycosphingolipids from epithelial cells of human stomach from seven individuals, a binding of H.pylori to the diglycosylceramide region of the non-acid fraction could be demonstrated in one of these cases. Mass spectrometry showed that the binding-active sample contained diglycosylceramides with phytosphingosine and 2-D hydroxy fatty acids with 16–24 carbon atoms in agreement with the results related above.