Borna disease of horses. An immunohistological and virological study of naturally infected animals.
Abstract: The brains of eight horses that had suffered from natural Borna disease were examined with virologic, immunohistological, and electron-microscopic methods. All brains harbored infectious virus as shown by inoculation of experimental animals. Regional assessment of the infectivity exhibited the highest titers in the hippocampus and piriform cortex and the lowest in the cerebellum. Conventional histology yielded pathologic alterations very similar to those of the classical description of the disease. Immunohistology demonstrated the highest amounts of Borna disease virus-specific antigen in the nuclei of neurons. In the perikarya, dendrites, and axons smaller amounts of antigen were found. A comparison of the antigen distribution with the inflammatory reaction established a high concordance of these two parameters. The presence of virus-specific antigen seems to trigger the exsudation of inflammatory cells, which reflect the extension of the infectious process. Heavy inflammatory exsudates in the white matter underlying diseased cortical areas can be explained by the axonal presence of virus-specific antigen. Virus particles could not be demonstrated with the electron microscope. The most significant findings at the ultrastructural level were stacks of fine filaments, adhering closely to cytoplasmic cisterns. These structures might be related to virus components or might be involved in virus morphogenesis.
Publication Date: 1984-01-01 PubMed ID: 6437125DOI: 10.1007/BF00688111Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This study investigates the presence and effects of Borna disease virus in horses, noting changes in brain tissue and regional differences in virus concentration. The researchers concluded that the virus triggers inflammation and identified unique subcellular structures potentially related to the virus.
Research Methodology
- The study utilized a range of methods including virology, immunohistology and electron microscopy to study the brains of eight horses affected by Borna disease.
- The researchers inoculated experimental animals with samples from various regions of the brain to determine the presence of infectious virus.
- They also conducted histological examinations to visualize pathological alterations linked to the virus.
Key Findings
- All examined brains were found to harbor the infectious Borna disease virus.
- The hippocampus and piriform cortex had the highest concentrations of the virus, whereas the cerebellum had the least.
- Immunohistology showed that virus-specific antigens are mainly present in the nuclei of neurons. Lesser amounts were found in perikarya, dendrites, and axons.
- The distribution of antigens was closely aligned with the regions of inflammation, indicating a correlation between the presence of virus-specific antigens and inflammatory reactions.
Implications
- The researchers suggest that the presence of virus-specific antigen appears to set off an inflammatory response, resulting in heavy inflammation in the white matter of affected areas.
- The findings propose that the observable pathology in brain tissue is due to this inflammatory response triggered by the presence of Borna disease virus.
- Although virus particles were not directly observed under electron microscopy, distinctive filament-like structures, potentially related to the virus, were identified in the cytoplasm.
Significance
- This study provides a depth of understanding on the infectivity and pathology of Borna disease in horses.
- The correlation between the presence of virus-specific antigens and the pathway triggering the inflammatory process offers new insights into how the Borna disease virus operates.
- This can lead to potential advancements in diagnosing and treating Borna disease in horses.
Cite This Article
APA
Gosztonyi G, Ludwig H.
(1984).
Borna disease of horses. An immunohistological and virological study of naturally infected animals.
Acta Neuropathol, 64(3), 213-221.
https://doi.org/10.1007/BF00688111 Publication
Researcher Affiliations
MeSH Terms
- Animals
- Antigens, Viral
- Borna Disease / immunology
- Borna Disease / microbiology
- Borna disease virus / immunology
- Borna disease virus / isolation & purification
- Brain / immunology
- Brain / microbiology
- Cytoskeleton / ultrastructure
- Horse Diseases / immunology
- Horses
- Viruses, Unclassified / immunology
References
This article includes 19 references
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Citations
This article has been cited 14 times.- Zhang Y, Alwin Prem Anand A, Bode L, Ludwig H, Emrich HM, Dietrich DE. Word recognition memory and serum levels of Borna disease virus specific circulating immune complexes in obsessive-compulsive disorder. BMC Psychiatry 2022 Sep 8;22(1):597.
- Hyndman TH, Shilton CM, Stenglein MD, Wellehan JFX Jr. Divergent bornaviruses from Australian carpet pythons with neurological disease date the origin of extant Bornaviridae prior to the end-Cretaceous extinction. PLoS Pathog 2018 Feb;14(2):e1006881.
- Zhang L, Lei Y, Liu X, Wang X, Liu Z, Li D, Zheng P, Zhang L, Chen S, Xie P. Glutamate and lipid metabolic perturbation in the hippocampi of asymptomatic borna disease virus-infected horses. PLoS One 2014;9(6):e99752.
- Schindler AR, Vögtlin A, Hilbe M, Puorger M, Zlinszky K, Ackermann M, Ehrensperger F. Reverse transcription real-time PCR assays for detection and quantification of Borna disease virus in diseased hosts. Mol Cell Probes 2007 Feb;21(1):47-55.
- Walker MP, Lipkin WI. Characterization of the nuclear localization signal of the borna disease virus polymerase. J Virol 2002 Aug;76(16):8460-7.
- Billaud JN, Ly C, Phillips TR, de la Torre JC. Borna disease virus persistence causes inhibition of glutamate uptake by feline primary cortical astrocytes. J Virol 2000 Nov;74(22):10438-46.
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- Zimmermann W, Breter H, Rudolph M, Ludwig H. Borna disease virus: immunoelectron microscopic characterization of cell-free virus and further information about the genome. J Virol 1994 Oct;68(10):6755-8.
- Lundgren AL, Lindberg R, Ludwig H, Gosztonyi G. Immunoreactivity of the central nervous system in cats with a Borna disease-like meningoencephalomyelitis (staggering disease). Acta Neuropathol 1995;90(2):184-93.
- Carbone KM, Duchala CS, Griffin JW, Kincaid AL, Narayan O. Pathogenesis of Borna disease in rats: evidence that intra-axonal spread is the major route for virus dissemination and the determinant for disease incubation. J Virol 1987 Nov;61(11):3431-40.
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- Stitz L, Sobbe M, Bilzer T. Preventive effects of early anti-CD4 or anti-CD8 treatment on Borna disease in rats. J Virol 1992 Jun;66(6):3316-23.
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- Vollmuth Y, Jungbäck N, Grochowski P, Mögele T, Stark L, Zarrabi NS, Schlegel J, Schaller T, Märkl B, Matiasek K, Liesche-Starnecker F. Mapping Bornavirus encephalitis-A comparative study of viral spread and immune response in human and animal dead-end hosts. PLoS Pathog 2025 Aug;21(8):e1013400.
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