Severe subcortical degeneration in macaques infected with neurovirulent simian immunodeficiency virus

Infection with human immunodeficiency virus-1 (HIV-1), the causative agent of acquired immunodeficiency syndrome (AIDS) in humans, causes a spectrum of neuropathology that includes alterations in behavior, changes in evoked potentials, and neuronal degeneration. In the simian immunodeficiency virus...

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Veröffentlicht in:Journal of neurovirology 2004-12, Vol.10 (6), p.387-399
Hauptverfasser: Marcario, JK, Manaye, KF, SantaCruz, KS, Mouton, PR, Berman, NEJ, Cheney, PD
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container_issue 6
container_start_page 387
container_title Journal of neurovirology
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creator Marcario, JK
Manaye, KF
SantaCruz, KS
Mouton, PR
Berman, NEJ
Cheney, PD
description Infection with human immunodeficiency virus-1 (HIV-1), the causative agent of acquired immunodeficiency syndrome (AIDS) in humans, causes a spectrum of neuropathology that includes alterations in behavior, changes in evoked potentials, and neuronal degeneration. In the simian immunodeficiency virus (SIV) model of HIV infection, affected monkeys show clinical symptoms and neurological complications that mimic those observed in human neuro-AIDS. To investigate the relationship between morphological correlates and neurophysiological deficits, unbiased stereology was used to assess total neuron number, volume, and neuronal density for all neurons in the globus pallidus (GP) and for dopamine (DA)-containing neurons in the substantia nigra (SN) in eight macaques inoculated with macrophage-tropic, neurovirulent SIV (SIVmac R71/17E), and five control animals. There was a significant difference between rapid progressors and controls for both neuron number (P
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In the simian immunodeficiency virus (SIV) model of HIV infection, affected monkeys show clinical symptoms and neurological complications that mimic those observed in human neuro-AIDS. To investigate the relationship between morphological correlates and neurophysiological deficits, unbiased stereology was used to assess total neuron number, volume, and neuronal density for all neurons in the globus pallidus (GP) and for dopamine (DA)-containing neurons in the substantia nigra (SN) in eight macaques inoculated with macrophage-tropic, neurovirulent SIV (SIVmac R71/17E), and five control animals. There was a significant difference between rapid progressors and controls for both neuron number (P &lt;. 01) and neuronal density (P &lt;. 05) in the GP, and for neuron number (P &lt;. 05) in the SN. Neuron loss ranged from 6% to 70% in the GP and from 10% to 50% in the SN. Neuropathological analyses confirmed neuroAIDS-like changes in brain, including microglial nodules, extensive perivascular cuffing and/or the presence of multinucleated giant cells, and alterations in neuronal morphology in the majority of the rapid progressors. By comparison, slow progressors showed little, if any, neuropathology. These neuropathological changes in SIV-infected monkeys indicate that neuron death and morphological alterations in the basal ganglia may contribute to the motor impairments reported in the SIV model and, by analogy, in the subset of patients afflicted with motor impairment in human neuro-AIDS.</description><identifier>ISSN: 1355-0284</identifier><identifier>EISSN: 1538-2443</identifier><identifier>DOI: 10.1080/13550280490521131</identifier><identifier>PMID: 15765810</identifier><language>eng</language><publisher>London: Informa UK Ltd</publisher><subject>Animals ; Basal Ganglia - pathology ; Basal Ganglia - virology ; Biological and medical sciences ; Brain - pathology ; Brain - virology ; Cell Count ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. 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Neuropathological analyses confirmed neuroAIDS-like changes in brain, including microglial nodules, extensive perivascular cuffing and/or the presence of multinucleated giant cells, and alterations in neuronal morphology in the majority of the rapid progressors. By comparison, slow progressors showed little, if any, neuropathology. These neuropathological changes in SIV-infected monkeys indicate that neuron death and morphological alterations in the basal ganglia may contribute to the motor impairments reported in the SIV model and, by analogy, in the subset of patients afflicted with motor impairment in human neuro-AIDS.</description><subject>Animals</subject><subject>Basal Ganglia - pathology</subject><subject>Basal Ganglia - virology</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Brain - virology</subject><subject>Cell Count</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Disease Progression</subject><subject>Globus Pallidus - pathology</subject><subject>Globus Pallidus - virology</subject><subject>Human immunodeficiency virus 1</subject><subject>Human viral diseases</subject><subject>Infectious diseases</subject><subject>Macaca</subject><subject>Macaca mulatta</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nerve Degeneration - pathology</subject><subject>Neurology</subject><subject>Neurons - pathology</subject><subject>Psychomotor Performance - physiology</subject><subject>Simian Acquired Immunodeficiency Syndrome - pathology</subject><subject>Simian Acquired Immunodeficiency Syndrome - physiopathology</subject><subject>Simian Immunodeficiency Virus</subject><subject>Substantia Nigra - pathology</subject><subject>Substantia Nigra - virology</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. 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Leukodystrophies. Prion diseases</topic><topic>Disease Progression</topic><topic>Globus Pallidus - pathology</topic><topic>Globus Pallidus - virology</topic><topic>Human immunodeficiency virus 1</topic><topic>Human viral diseases</topic><topic>Infectious diseases</topic><topic>Macaca</topic><topic>Macaca mulatta</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nerve Degeneration - pathology</topic><topic>Neurology</topic><topic>Neurons - pathology</topic><topic>Psychomotor Performance - physiology</topic><topic>Simian Acquired Immunodeficiency Syndrome - pathology</topic><topic>Simian Acquired Immunodeficiency Syndrome - physiopathology</topic><topic>Simian Immunodeficiency Virus</topic><topic>Substantia Nigra - pathology</topic><topic>Substantia Nigra - virology</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. 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source Taylor & Francis; MEDLINE; Springer Nature - Complete Springer Journals
subjects Animals
Basal Ganglia - pathology
Basal Ganglia - virology
Biological and medical sciences
Brain - pathology
Brain - virology
Cell Count
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Disease Progression
Globus Pallidus - pathology
Globus Pallidus - virology
Human immunodeficiency virus 1
Human viral diseases
Infectious diseases
Macaca
Macaca mulatta
Male
Medical sciences
Nerve Degeneration - pathology
Neurology
Neurons - pathology
Psychomotor Performance - physiology
Simian Acquired Immunodeficiency Syndrome - pathology
Simian Acquired Immunodeficiency Syndrome - physiopathology
Simian Immunodeficiency Virus
Substantia Nigra - pathology
Substantia Nigra - virology
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral diseases of the nervous system
title Severe subcortical degeneration in macaques infected with neurovirulent simian immunodeficiency virus
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