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Science 24 June 1983:
Vol. 220. no. 4604, pp. 1401 - 1403
DOI: 10.1126/science.6602380

Articles

Science, Vol 220, Issue 4604, 1401-1403
Copyright © 1983 by American Association for the Advancement of Science


articles

Behavioral disease in rats caused by immunopathological responses to persistent borna virus in the brain

O Narayan, S Herzog, K Frese, H Scheefers, and R Rott

Borna virus replicated persistently in the brains of rats, causing frenzied and apathetic behavioral states in sequence but no mortality. The transient frenzied behavior was caused by an immune-mediated, cytolytic, encephalitic response that was unexpectedly self-limiting. Cessation of active pathological processes coincided with the onset of the passive phase of the disease. This study thus demonstrates suppression of virus-specific inflammation despite continuous viral replication and describes a new mechanism by which chronic encephalitis may become established.


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Enhanced Neurovirulence of Borna Disease Virus Variants Associated with Nucleotide Changes in the Glycoprotein and L Polymerase Genes.
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1-{beta}-D-Arabinofuranosylcytosine Inhibits Borna Disease Virus Replication and Spread.
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Varied Persistent Life Cycles of Borna Disease Virus in a Human Oligodendroglioma Cell Line.
M. S. Ibrahim, M. Watanabe, J. A. Palacios, W. Kamitani, S. Komoto, T. Kobayashi, K. Tomonaga, and K. Ikuta (2002)
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CD8+ T Lymphocytes Mediate Borna Disease Virus-Induced Immunopathology Independently of Perforin.
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Identification of the Immunodominant H-2Kk-Restricted Cytotoxic T-Cell Epitope in the Borna Disease Virus Nucleoprotein.
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Synaptic Pathology in Borna Disease Virus Persistent Infection.
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J. Virol. 74, 3441-3448
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Inhibition of Borna Disease Virus Replication by Ribavirin.
I. Jordan, T. Briese, D. R. Averett, and W. I. Lipkin (1999)
J. Virol. 73, 7903-7906
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T cell ignorance in mice to Borna disease virus can be overcome by peripheral expression of the viral nucleoprotein.
J. Hausmann, W. Hallensleben, J. C. de la Torre, A. Pagenstecher, C. Zimmermann, H. Pircher, and P. Staeheli (1999)
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Effect of Immune Priming on Borna Disease.
A. J. Lewis, J. L. Whitton, C. G. Hatalski, H. Weissenbock, and W. I. Lipkin (1999)
J. Virol. 73, 2541-2546
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Borna Disease Virus Nucleoprotein (p40) Is a Major Target for CD8+-T-Cell-Mediated Immune Response.
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J. Virol. 73, 1715-1718
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Y. Iwata, K. Takahashi, X. Peng, K. Fukuda, K. Ohno, T. Ogawa, K. Gonda, N. Mori, S.-i. Niwa, and S. Shigeta (1998)
J. Virol. 72, 10044-10049
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Borna Disease Virus-Induced Neurological Disorder in Mice: Infection of Neonates Results in Immunopathology.
W. Hallensleben, M. Schwemmle, J. Hausmann, L. Stitz, B. Volk, A. Pagenstecher, and P. Staeheli (1998)
J. Virol. 72, 4379-4386
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Virus-Specific CD4+ T Cells Eliminate Borna Disease Virus from the Brain via Induction of Cytotoxic CD8+ T Cells.
K. Noske, T. Bilzer, O. Planz, and L. Stitz (1998)
J. Virol. 72, 4387-4395
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Interactions of the Borna Disease Virus P, N, and X Proteins and Their Functional Implications.
M. Schwemmle, M. Salvatore, L. Shi, J. Richt, C. H. Lee, and W. I. Lipkin (1998)
J. Biol. Chem. 273, 9007-9012
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A borna virus cDNA encoding a protein recognized by antibodies in humans with behavioral diseases.
S VandeWoude, J. Richt, M. Zink, R Rott, O Narayan, and J. Clements (1990)
Science 250, 1278-1281
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Borna Disease Virus: A Possible Etiologic Factor in Human Affective Disorders?.
J. D. Amsterdam, A. Winokur, W. Dyson, S. Herzog, F. Gonzalez, R. Rott, and H. Koprowski (1985)
Arch Gen Psychiatry 42, 1093-1096
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Detection of serum antibodies to Borna disease virus in patients with psychiatric disorders.
R Rott, S Herzog, B Fleischer, A Winokur, J Amsterdam, W Dyson, and H Koprowski (1985)
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Borna Disease Virus Persistent Infection Activates Mitogen-activated Protein Kinase and Blocks Neuronal Differentiation of PC12 Cells.
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