This article describes the main aspects of bovine herpesvirus type-5 (BHV-5
) neurologic infection and disease in rabbits, a candidate animal model for
studying BHV-5 neuropathogenesis. Intranasal inoculation of weanling rabbi
ts with a Brazilian BHV-5 isolate produced neurological disease and death i
n 78.8% (26/33) of the animals. Neurological signs started as early as 5 da
ys post-inoculation and lasted from 10-12 hours up to several days. Most an
imals evolved to a moribund state or death within 24 (69.2%) to 48 hours (8
8.5%). Neurological disease was characterized by excitability or depression
, tremors, bruxism, walking or running in circles, backward arching of the
head and body, incoordination, backward and sideways falling, paddling, pro
found depression and death. Moderate levels of infectivity were detected in
several areas of the brain, most consistently in the ventro-lateral hemisp
here (in 16 out of 20 animals), anterior cerebrum (15/20), midbrain (11/20)
, dorso-lateral hemisphere (10/20) and pens (12/26). Infectious virus was a
lso recovered from the olfactory bulb (9/20), medulla oblongata (10/26), ce
rebellum (7/20), posterior cerebrum (5/20) and trigeminal ganglia (4/20). N
o gross lesions were observed. Microscopic lesions were mild and consisted
of nonsuppurative meningitis, mononuclear perivascular cuffing and focal gl
iosis. These changes were observed most consistently in the ventro-lateral
hemisphere and anterior cerebrum. Passive immunity partially protected rabb
its from BHV-5-induced encephalitis. Rabbits born to immunized dams showed
a significative delay in the onset of clinical disease and reduced morbidit
y and mortality rates compared to rabbits born to unvaccinated dams. These
results demonstrate that BHV-5-induced neurological disease can consistentl
y be reproduced in rabbits and point towards the use of this species as an
animal model to study BHV-5 neuropathogenesis.