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Journal of Virology, November 1998, p. 9109-9115, Vol. 72, No. 11
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Neurovirulence in Feline Immunodeficiency Virus-Infected Neonatal
Cats Is Viral Strain Specific and Dependent on Systemic
Immune Suppression
C.
Power,1,*
R.
Buist,2
J. B.
Johnston,1
M. R.
Del
Bigio,3
W.
Ni,1
M. R.
Dawood,4 and
J.
Peeling3
Department of Clinical
Neurosciences,1 University of Calgary, Calgary,
Alberta T2N 4N1, and
Departments of
Radiology,2
Pathology,3 and
Medical
Microbiology,4 University of Manitoba,
Winnipeg, Manitoba R3E 0W3, Canada
Received 13 May 1998/Accepted 6 August 1998
Feline immunodeficiency virus (FIV) is a lentivirus that causes
immune suppression and neurological disease in cats. Among animal
viruses, individual viral strains have been shown to be neurovirulent,
but the role of viral strain specificity among lentiviruses and its
relationship to systemic immune suppression in the
development of neurological disease remains uncertain. To
determine the extent to which different FIV strains caused neurological disease, FIV V1CSF and Petaluma were compared in ex vivo
assays and in vivo. Both viruses infected and replicated in macrophage
and mixed glial cell cultures at similar levels, but V1CSF
induced significantly greater neuronal death than Petaluma in a
neurotoxicity assay. V1CSF-infected animals showed significant neurodevelopmental delay compared to the Petaluma-infected and uninfected animals. Magnetic resonance spectroscopy
studies of frontal cortex revealed significantly reduced
N-acetyl aspartate/creatine ratios in the V1CSF
group compared to the other groups. Cyclosporin A treatment of
Petaluma-infected animals caused neurodevelopmental delay and reduced
N-acetyl aspartate/creatine ratios in the brain. Reduced
CD4+ and CD8+ cell counts were observed in the
V1CSF-infected group compared to the uninfected and
Petaluma-infected groups. These findings suggest that
neurodevelopmental delay and neuronal injury is FIV strain
specific but that systemic immune suppression is also an important determinant of FIV-induced neurovirulence.
*
Corresponding author. Mailing address: Department of
Clinical Neurosciences, University of Calgary, Heritage Medical
Building, 107-3330 Hospital Dr., Calgary, AB Canada T2N 4N1. Phone:
(403) 220-5011. Fax: (403) 283-8731. E-mail:
power{at}ucalgary.ca.
Journal of Virology, November 1998, p. 9109-9115, Vol. 72, No. 11
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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