Neospora caninum is a cyst-forming coccidian parasite which in cattle can c
ause abortion and birth of feeble calves. For the serological diagnosis of
neosporosis, antibodies directed to the parasite can be demonstrated by ELI
SA, utilizing N. caninum proteins incorporated into iscoms (immunostimulati
ng complexes) as antigen. Electrophoretic and immunoblotting studies had ea
rlier revealed that N. caninum iscoms contained a restricted number of prot
eins compared with soluble parasite extracts, but the cellular origin of th
e incorporated proteins has not yet been determined. In the present study,
monoclonal antibodies were raised against N. caninum iscoms. Six of these,
named Ncmab-4, 7, 10, 13, 17 and 24, were used to characterize the N. canin
um iscom antigen. The nature of the reactive epitopes and their localizatio
n within N. caninum tachyzoites were determined by means of immunological m
ethods, including immunoblot, IFAT and immunogold electron microscopy. The
apparent molecular weights of the dominant iscom antigens were found to be
18, 30, 32, 41 and 61 kDa. While the 61 kDa antigen was located intracellul
arly, the others were found on the parasite surface as well as within disti
nct intracellular compartments.