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Journal ArticleDOI

In Vivo and In Vitro Models of Demyelinating Diseases: III. JHM Virus Infection of Rats

O. Sorensen, +2 more
- 01 Aug 1980 - 
- Vol. 37, Iss: 8, pp 478-484
TLDR
The JHMV-infected rat seems to be an appropriate animal model to study virus-mediated progressive demyelinating disease and occasionally, clinical remissions were observed in rats in which posterior paralysis developed, suggesting that remyelination in the rat can occur.
Abstract
• Suckling rats of three inbred and three outbred strains were inoculated intraperitoneally (IP) or intracerebrally (IC) with the JHM strain of mouse hepatitis virus (JHMV) and were monitored for evidence of neurologic diseases. Consequences of varying age at inoculation, route of injection, and virus dose were ascertained. No disease was evident after IP injection but IC inoculation with at least 10 4 plaque-forming units at 2 days of age resulted in either a rapidly fatal encephalitis or a chronic, progressive, fatal neurologic disease in most rats, regardless of strain. Inoculation at 5 or 10 days of age predominantly caused the chronic neurologic disease, characterized by demyelinating lesions in the brain, spinal cord, or optic nerve, which sometimes were evident as late as several months postinoculation. Demyelination in the optic nerve proved to be concurrent with demyelinating lesions elsewhere in the CNS. Occasionally, clinical remissions were observed in rats in which posterior paralysis developed, suggesting that remyelination in the rat can occur. Demonstration of virus replication, by infectivity, in rats exhibiting neurologic disease and in rats without clinical symptoms was substantiated by electron microscopic observations of virus development and assembly in oligodendroglia of the optic nerve and spinal cord. In view of the protracted course of the disease in some rats, presence of demyelinating lesions confirmed by light and electron microscopy, and remissions of clinical symptoms, the JHMV-infected rat seems to be an appropriate animal model to study virusmediated progressive demyelinating disease.

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Citations
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Isolation and direct characterization of resident microglial cells from the normal and inflamed central nervous system.

TL;DR: Using irradiation chimeras, it is shown that resident microglia respond to inflammation by upregulating CD45, CD4, and MHC class I molecules with a minority of these cells increasing their expression of MHCclass II molecules.
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The Biology and Pathogenesis of Coronaviruses

TL;DR: The coronavirases were first recognized and morphologically defined as a group by Tyrrell and co-workers (1968, 1975, 1978) and biochemical studies have recently provided additional information which allows better characterization of these agents.
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Pathogenicity of antigenic variants of murine coronavirus JHM selected with monoclonal antibodies.

TL;DR: To analyze the pathogenesis of the neurotropic murine coronavirus JHMV, monoclonal antibodies to the E2 viral glycoprotein were used to select antigenic variant viruses and demyelinating variants with reduced neurovirulence were selected.
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The biology of coronaviruses.

TL;DR: The Coronaviridae is a monogeneric family comprising 11 viruses which infect vertebrates and was originally recognized on the basis of a characteristic virion morphology, but can now be defined by biological and molecular criteria.
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Adoptive transfer of EAE-like lesions from rats with coronavirus-induced demyelinating encephalomyelitis

TL;DR: The occurrence of cell-mediated immune reactions against basic myelin proteins in the course of coronavirus infections in Lewis rats demonstrates that a virus infection in CNS tissue is capable of initiating an autoimmune response which may be of pathogenic importance.
References
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Book

Manual of histologic staining methods of the Armed forces institute of pathology

Lee G Luna
TL;DR: This work states that stem cells: mechanisms of inflammation,” Annual Review of Pathology, vol.
Journal ArticleDOI

Glial cells and the central myelin sheath.

R P Bunge
Journal ArticleDOI

A murine virus (JHM) causing disseminated encephalomyelitis with extensive destruction of myelin.

TL;DR: A description has been given of the pathologic changes produced experimentally in animals by the inoculation of a virus material obtained from a mouse with spontaneous encephalomyelitis, which includes the widespread destruction of myelin.
Journal ArticleDOI

Pathogenesis of demyelination induced by a mouse hepatitis.

Leslie P. Weiner
- 01 May 1973 - 
TL;DR: Demyelinative lesions produced in mice by inoculation of JHM virus, a neurotropic strain of mouse hepatitis virus, appeared to be the direct result of infection of glial cells of the white matter.
Journal ArticleDOI

Mechanism of demyelination in JHM virus encephalomyelitis. Electron microscopic studies.

TL;DR: The findings indicate that JHM virus has an affinity for oligodendrocytes in weanling mice and that demyelination occurs subsequently to the degeneration of the infected oligodends, and that the myelin sheaths disintegrated or were stripped off intact axons by cytoplasmic tongues of polymorpho- and mononuclear leucocytes that intruded between myelin lamellae.
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