AI Article Synopsis

  • Non-mammalian cell wall sugars are structurally similar across various pathogenic bacteria, making them attractive candidates for vaccine development due to their distinctiveness from mammalian sugars.
  • A glycoconjugate featuring Gram-negative bacterial 'inner core' sugars was synthesized, aiming to enhance immunization effectiveness.
  • The study demonstrates that this glycoconjugate, when used alongside a transport inhibitor, can stimulate antibody production and significantly improve bacterial killing against major pathogens like Neisseria meningitidis and Escherichia coli.

Article Abstract

Certain non-mammalian cell wall sugars are conserved across a variety of pathogenic bacteria. This conservation of structure, combined with their structural differences when compared with mammalian sugars, make them potentially powerful epitopes for immunization. Here, we report the synthesis of a glycoconjugate that displays the so-called 'inner core' sugars of Gram-negative bacterial cell walls. We also describe an antibacterial vaccination strategy based on immunization with the glycoconjugate and the subsequent administration of an inhibitor that uncovers the corresponding epitope in pathogenic bacteria. The core tetrasaccharide, Hep2Kdo2, a common motif in bacterial lipopolysaccharides, was synthesized and attached via a chain linker to a diphtheria toxin mutant carrier protein. This glycoconjugate generated titres of antibodies towards the inner core tetrasaccharide of the lipopolysaccharide, which were capable of binding the cell-surface sugars of bacterial pathogenic strains including Neisseria meningitidis, Pseudomonas aeruginosa and Escherichia coli. Exposure of bacterial lipopolysaccharide in in vitro experiments, using an inhibitor of capsular polysaccharide transport, enabled potent bacterial killing with antiserum.

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Source
http://dx.doi.org/10.1038/nchem.2432DOI Listing

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