Pathogenesis of SIV encephalitis: Selection and replication of neurovirulent SIV

Mary Christine Zink, Angela Martin Amedee, Joseph L Mankowski, Linden Craig, Peter Didier, Darryl L. Carter, Alvaro Munoz, Michael Murphey-Corb, Janice E Clements

Research output: Contribution to journalArticle

Abstract

To investigate the viral and host factors that contribute to neurological disease, nine macaques were intravenously co-inoculated with SIV/DeltaB670, a primary isolate of SIV consisting of at least 21 different genotypes, and SIV/17E-Fr, a neurovirulent recombinant clone. CD4+ cell counts and antigenemia were measured throughout infection. The SIV env V1 region was amplified from brain and peripheral blood mononuclear cell DNA to compare the genotypes present in brain and blood. Seven of the 9 macaques (78%) developed typical SIV-associated neurological lesions classified as severe (4 macaques), moderate (2 macaques), or mild (1 macaque) with a mean time to euthanasia of 7 months. Macaques with severe neurological lesions progressed more rapidly, with a mean time to euthanasia of 3.6 months. SIV/17E-Fr was detected in brain homogenates from all four macaques with severe encephalitis, and in three of the four, SIV/17E-Fr was the only genotype identified in the central nervous system. Macaques with less severe or no neurological lesions usually had one of various genotypes of SIV/DeltaB670 in brain. A variety of genotypes of SIV/DeltaB670 and SIV/17E- Fr were detected in peripheral blood mononuclear cells throughout infection. Macaques with severe neurological lesions had the most precipitous declines in CD4+ cell counts, the highest levels of antigenemia, and the greatest expression of viral RNA and protein in the central nervous system. Macaca nemestrina were more likely to develop severe neurological lesions than M. mulatta or M. fascicularis (p = 0.048). This study demonstrated that neurovirulent strains within the virus swarm can selectively enter and become established in the central nervous system and that the neurological lesions that develop are correlated with the development of host immunosuppression. The species differences in severity of neurological lesions seen in this study suggest that host factors are also important in determining the outcome of lentiviral infection.

Original languageEnglish (US)
Pages (from-to)793-803
Number of pages11
JournalAmerican Journal of Pathology
Volume151
Issue number3
StatePublished - Sep 1997

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Macaca
Encephalitis
Genotype
Euthanasia
Central Nervous System
Brain
CD4 Lymphocyte Count
Blood Cells
Infection
Macaca nemestrina
Viral RNA
Viral Proteins
Immunosuppression
Clone Cells
Viruses
DNA

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Cite this

Pathogenesis of SIV encephalitis : Selection and replication of neurovirulent SIV. / Zink, Mary Christine; Amedee, Angela Martin; Mankowski, Joseph L; Craig, Linden; Didier, Peter; Carter, Darryl L.; Munoz, Alvaro; Murphey-Corb, Michael; Clements, Janice E.

In: American Journal of Pathology, Vol. 151, No. 3, 09.1997, p. 793-803.

Research output: Contribution to journalArticle

Zink, Mary Christine ; Amedee, Angela Martin ; Mankowski, Joseph L ; Craig, Linden ; Didier, Peter ; Carter, Darryl L. ; Munoz, Alvaro ; Murphey-Corb, Michael ; Clements, Janice E. / Pathogenesis of SIV encephalitis : Selection and replication of neurovirulent SIV. In: American Journal of Pathology. 1997 ; Vol. 151, No. 3. pp. 793-803.
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