A sandwich enzyme-linked immunosorbent assay (ELISA) for the sensitive and
specific detection of bovine antibodies to Neospora caninum was developed a
nd evaluated using sera from cattle experimentally infected with N. caninum
. Toxoplasma gondii. Sarcocystis cruzi, Sarcocystis hominis, Sarcocystis hi
rsuta, Eimeria bovis, Cryptosporidium parvum, Babesia divergens. and field
sera from naturally exposed animals. Field sera were classified using a gol
d standard that included the results from an indirect fluorescent antibody
rest (IFAT) and an immunoblot (IB). Based on these gold standard results, i
.e., IFAT-IB results, an equal relative sensitivity and specificity of 94.2
% (theta(0),) was reached when a cutoff of 0.034 (d(0))was employed. The an
alysis of IFAT-IB-positive held sera showed that within groups of aborting
and nonaborting dams, the animals from herds with endemic N. caninum-associ
ated abortions had significantly higher ELISA indices than animals from her
ds with N. caninum-associated, epidemic abortions. By contrast, IFAT-IBposi
tive aborting dams from herds with endemic N. caninum,-associated abortions
had significantly lower IFAT titers than IFAT-IBpositive abetting dams fro
m herds with epidemic N. caninum-associated abortions. This is the first ti
me that statistically significant serological, differences between herds ex
hibiting epidemic and endemic N. canimum-associated abortions are described
.