Neospora hughesi is a recently described cause of equine protozoal myeloenc
ephalitis (EPM). A rodent model for pathogenicity would facilitate developm
ent of therapies to be used in horses. In the present study, we examined th
e susceptibility of BALB/c gamma-interferon gene knockout (gamma-INFKO), BA
LB/c, CD-1, and C57BL/6 strains of mice and gerbils to infection with tachy
zoites of the Nh-A1 strain of N. hughesi isolated from a horse from AL, USA
. Only the gamma-IFNKO mice developed severe clinical disease following inf
ection with N. hughesi and died 19-25 days after infection and exhibited se
vere cardiac lesions. In contrast, experimental infection of gamma-INFKO mi
ce with tachyzoites of the NC-1 or NC-Liverpool strains of Neospora caninum
resulted in deaths 8-10 days after infection. The most severe lesions were
in the livers, spleens, and lungs of these mice. Gerbils inoculated with N
. hughesi did not develop clinical disease, had few microscopic lesions, bu
t did seroconvert. Two dogs fed the brains of mice, shown to contain N, hug
hesi tissue stages by cell culture and gamma-IFNKO mouse bioassay, did not
shed N, caninum-like oocysts over a 23 days observation period. The marked
difference in pathogenicity between the two species of Neospora in gamma-IF
NKO mice, and lack of oocyst excretion by dogs fed N, hughesi infected mice
provide additional evidence that the species distinction between N. caninu
m and N. hughesi is valid. (C) 2000 Elsevier Science B.V. All rights reserv
ed.