Nasal Immunization with the C-Terminal Domain of Bcla3 Induced Specific IgG Production and Attenuated Disease Symptoms in Mice Infected with Spores.

is a Gram-positive, spore-forming bacterium that causes a severe intestinal infection. Spores of this pathogen enter in the human body through the oral route, interact with intestinal epithelial cells and persist in the gut. Once germinated, the vegetative cells colonize the intestine and produce toxins that enhance an immune response that perpetuate the disease. Therefore, spores are major players of the infection and ideal targets for new therapies. In this context, spore surface proteins of are potential antigens for the development of vaccines targeting spores. Here, we report that the C-terminal domain of the spore surface protein BclA3, BclA3, was identified as an antigenic epitope, over-produced in and tested as an immunogen in mice. To increase antigen stability and efficiency, BclA3 was also exposed on the surface of spores, a mucosal vaccine delivery system. In the experimental conditions used in this study, free BclA3 induced antibody production in mice and attenuated some infection symptoms after a challenge with the pathogen, while the spore-displayed antigen resulted less effective. Although dose regimen and immunization routes need to be optimized, our results suggest BclA3 as a potentially effective antigen to develop a new vaccination strategy targeting spores.