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Clostridioides difficile is the primary cause of antibiotic-associated diarrhea and colitis, a healthcare-associated intestinal disease resulting in a significant fatality rate. Colonization of the gut is critical for C. difficile pathogenesis. The bacterial molecules essential for efficient colonization therefore offer great potential as vaccine candidates. Here we present findings demonstrating that the C. difficile immunogenic lipoprotein CD0873 plays a critical role in pathogen success in vivo We found that in a dixenic colonization model, a CD0873-positive strain of C. difficile significantly outcompeted a CD0873-negative strain. Immunization of mice with recombinant CD0873 prevented long-term gut colonization and was correlated with a strong secretory IgA immune response. We further present high-resolution crystal structures of CD0873, at 1.35-2.50 Å resolutions, offering a first view of the ligand-binding pocket of CD0873 and provide evidence that this lipoprotein adhesin is part of a tyrosine import system, an amino acid key in C. difficile infection. These findings suggest that CD0873 could serve as an effective component in a vaccine against C. difficile.

More information Original publication

DOI

10.1074/jbc.RA119.010120

Type

Journal article

Publication Date

2019-10-25T00:00:00+00:00

Volume

294

Pages

15850 - 15861

Total pages

11

Keywords

ABC transporter, Clostridioides difficile, crystallography, microbiology, protein structure, tyrosine metabolism, vaccine, Animals, Bacterial Vaccines, Clostridioides difficile, Clostridium Infections, Colony Count, Microbial, Disease Models, Animal, Female, Humans, Immunization, Immunoglobulin A, Secretory, Intestines, Ligands, Lipoproteins, Mice, Inbred C57BL, Mutation, Recombinant Proteins