| Literature DB >> 22620974 |
Roberto Adamo1, Maria R Romano, Francesco Berti, Rosanna Leuzzi, Marta Tontini, Elisa Danieli, Emilia Cappelletti, Osman S Cakici, Erwin Swennen, Vittoria Pinto, Barbara Brogioni, Daniela Proietti, Cesira L Galeotti, Luigi Lay, Mario A Monteiro, Maria Scarselli, Paolo Costantino.
Abstract
Clostridium difficile is emerging worldwide as a major cause of nosocomial infections. The negatively charged PSII polysaccharide has been found in different strains of C. difficile and, thereby, represents an important target molecule for a possible carbohydrate-based vaccine. In order to identify a synthetic fragment that after conjugation to a protein carrier could be able to induce anti-PSII antibodies, we exploited a combination of chemical synthesis with immunochemistry, confocal immunofluorescence microscopy, and solid state NMR. We demonstrate that the phosphate group is crucial in synthetic glycans to mimic the native PSII polysaccharide; both native PSII and a phosphorylated synthetic hexasaccharide repeating unit conjugated to CRM(197) elicit comparable immunogenic responses in mice. This finding can aid design and selection of carbohydrate antigens to be explored as vaccine candidates.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22620974 DOI: 10.1021/cb300221f
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100