Neospora caninum is a protozoan parasite that causes severe disease in
transplacentally infected dogs and abortions in domestic ruminants. R
odent models of neosporosis rely on treatment of hosts with methylpred
nisolone acetate (MPA) to enhance infections. The present study report
s the development of an inbred BALB/c mouse model that results in cent
ral nervous system neosporosis in the absence of MPA treatment. Seven
of 12 BALB/c mice died 26-70 days after subcutaneous (s.c.) inoculatio
n with tachyzoites of the NC-1 strain of N. caninum, and none of 12 BA
LB/c mice died after s.c. inoculation with tachyzoites of the NC-3 str
ain. None of 8 HSD:ICR mice (4 mice, NC-1 strain; 4 mice, NC-3 strain)
developed clinical neosporosis or died after s.c. inoculation with ta
chyzoites. Control BALB/c (2) and HSD:ICR (2) mice s.c. inoculated wit
h Hanks' balanced salt solution did not develop clinical signs of dise
ase. Some mice in all N. caninum-inoculated groups had brain lesions,
but significantly (P < 0.05) more BALB/c mice inoculated with the NC-1
strain had brain lesions.