Borna disease is a neurologic syndrome caused by infection with a nons
egmented, negative strand RNA virus, Borna disease virus. Infected ani
mals have antibodies to two soluble viral proteins, p40 and p23, and a
membrane-associated viral glycoprotein, gp18. We examined the time co
urse for the development of neutralization activity and the expression
of antibodies to individual viral proteins in sera of infected rats.
The appearance of neutralizing activity correlated with the developmen
t of immunoreactivity to gp18, but not p40 or p23. Monospecific and mo
noclonal antibodies to native gp18 and recombinant nonglycosylated gp1
8 were also found to have neutralizing activity and to immunoprecipita
te viral particles or subparticles. These findings suggest that gp18 i
s likely to be present on the surface of the viral particles and is li
kely to contain epitopes important for virus neutralization.