-Demonstrated that M cells are the main route of TSE agent uptake from the small intestine after oral exposure.
-Demonstrated for the first time that distinct mechanisms regulate the development of the GALT in the large and small intestines.
-Demonstrated for the first time that the large intestine is not a primary site of TSE agent neuroinvasion after oral exposure.
-Demonstrated for the first time that congruent parasite infection in the large intestine does not influence oral TSE pathogenesis or susceptibility.
-Demonstrated for the first time that a congruent parasite infection in the large intestine can exacerbate the onset of clinical TSE disease.
-Project still in progress and will be published as soon as ready.