Structural and immunological characterization of a glycoconjugate based on the delipidated lipopolysaccharide from a nontypeable Helicobacter pylori strain PJ1 containing an extended D-glycero-D-manno-heptan

Structural characterization of the lipopolysaccharide (LPS) from a nontypeable Helicobacter pylori strain PJ1 and two corresponding mutants, PJ1 HP1283:cam and PJ1 HP1284:cam, was performed using a combination of NMR and mass spectrometric techniques. It resulted in the core structure that differed significantly from the one proposed previously. Overall architecture of PJ1 LPS was found to be consistent with a structural model described for several other H. pylori strains. It contained a polymer of D-glycero-D-manno- heptose (DD-Hep) as the O-chain component, linked to alpha-1,6-glucan through a DD-Hep oligosaccharide. H. pylori PJ1 HP1283:cam LPS was missing DD-heptan, terminating with an alpha-1,6-glucan chain containing 5e13 glucose residues. LPS of strain PJ1 HP1284:cam was missing DD-Hep from the core and had beta-GlcNAc attached directly to O-3 of the inner-core LD-Hep residue. To investigate the role of D-Dheptan in protective immunity, delipidated LPS (dLPS) from strain PJ1 was conjugated to tetanus toxoid (TT) and immunological properties of the resultant glycoconjugate dLPS(PJ1)-TT determined. The dLPS(PJ1)-TT conjugate was immunogenic in mice and rabbits and induced specific and cross-reactive functional antibodies against homologous and heterologous strains of H. pylori. Whole cell indirect ELISA performed on a selected number of H. pylori isolates confirmed that the immune response correlated with the presence of alpha-1,6-glucan and was not augmented by the DD-Hep content of these strains. Crown Copyright (c) 2017 Published by Elsevier Ltd. All rights reserved.