Tr. Phillips et al., NEUROLOGIC DYSFUNCTIONS CAUSED BY A MOLECULAR CLONE OF FELINE IMMUNODEFICIENCY VIRUS, FIV-PPR, Journal of neurovirology, 2(6), 1996, pp. 388-396
FIV is a lentivirus of domestic cats that causes a spectrum of disease
s that is remarkably similar to the clinical syndrome produced by HIV
infection in people. Both HEV and FIV has been shown to cause neurolog
ic dysfunction. Specific Pathogen-Free (SPF) cats were placed into one
of three groups: FIV-PPR infected; DU-FIV-PPR (a dUTPase mutant of th
e FIV-PPR clone) infected; or an age-matched control group. In both in
fested groups, the general clinical signs of infection included lympha
denopathy, oral ulcerations, rough hair coat, and conjuntivitis. Speci
fic neurological changes in the FIV-PPR infected cats included hind li
mb paresis; delayed righting and pupillary reflexes; behavioral change
s; delayed visual and auditory evoked potentials; decreased spinal and
peripheral nerve conduction velocities; and marked alterations in sle
ep patterns, Most of these changes were also observed in the DU-FIV-PP
R infected cats. However, these cats tended to have a slightly less se
vere disease. In this study, we have demonstrated that an infectious m
olecular clone of FIV closely parallels the disease course of wild typ
e FIV-infected cats. By using a knockout gene mutant of this clone, we
were able to demonstrate that the dUTPase gene is not essential for n
europathogenesis. Further use of the FIV-PPR clone should prove useful
in determining the essential viral elements that are important in the
neuropathogenesis of lentiviral infections.