Some strains of bluetongue virus cause congenital brain damage in bovi
ne and ovine fetuses, as well as in neonatal mice. Two strains of blue
tongue virus serotype 11 (UC-2 and UC-8) which differ in neuroinvasive
ness were used to determine the biological basis for this difference.
UC-2 and UC-8 were inoculated subcutaneously into newborn mice and vir
us was titrated from blood, plasma and brain tissues over 14 days. For
the invasive UC-8 strain, 50-175 plaque forming units of virus per ml
was found associated with the blood cells and no virus was detected i
n the plasma. The virus was detected in the brain at day one post inoc
ulation, and again at day 7, increasing to day 11. The results indicat
e that UC-8 was able to reach the brain soon after inoculation and to
replicate and/or remain in the blood circulation better than UC-2. Imm
unohistochemical examination of frozen brain sections revealed a sudde
n, multifocal appearance of UC-8 at day 9, with more viral antigen see
n at days 11 and 13, which was barely detected by day 15. Viral antige
n was not associated with blood vessels in the brain, indicating that
the viral invasion was not from infected vascular endothelium. No viru
s was detected in the mice infected with strain UC-2.