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Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues
Published on: May 8, 2016
Theiler's murine encephalomyelitis virus 3D RNA polymerase: its expression in the CNS and the specific immune
I C Johnston1, E J Usherwood, A A Nash
1Department of Pathology, University of Cambridge, UK.
Abstract:
Intracerebral inoculation of the neurotropic murine picornavirus, Theiler's murine encephalomyelitis virus (TMEV), results either in an acute encephalitis (GDVII strain) or in the establishment of a persistent infection with the development of demyelinating lesions (BeAn strain). In this article, the expression of the viral RNA polymerase was studied in the central nervous system of both acutely and persistently infected mice and in infected cells in tissue culture. Similar numbers of acutely infected glial cells (80-85%) expressed both viral polymerase and structural proteins in vitro while a much smaller proportion of persistently infected glial cells (0.6-0.9%) expressed these proteins. Following infection of mice with GDVII, many cells in the brain were found to express polymerase. However, in the spinal cord of mice persistently infected with BeAn, very few cells were found to express the polymerase while many more cells showed the presence of viral structural proteins. This suggests that a restriction in viral replication, possibly at the level of polymerase expression, may be a feature of the persistent infection. However, enough polymerase was expressed to maintain a polymerase-specific antibody response in a number of infected animals as late as 21 months post-infection. Mechanisms that may be involved in the establishment and maintenance of TMEV persistence are discussed with reference to these findings.
Insights
Theiler
Area of Science:
- Neurovirology
- Immunology
Background:
- Theiler's murine encephalomyelitis virus (TMEV) causes acute encephalitis or persistent demyelinating infections.
- Viral RNA polymerase is crucial for picornavirus replication.
Purpose of the Study:
- To investigate viral RNA polymerase expression in TMEV-induced acute and persistent central nervous system (CNS) infections.
- To explore the role of polymerase expression in TMEV persistence.
Main Methods:
- Intracerebral inoculation of mice with TMEV strains GDVII (acute) and BeAn (persistent).
- Analysis of viral RNA polymerase and structural protein expression in CNS tissues and infected glial cells in vitro.
- Detection of polymerase-specific antibodies.
Main Results:
- Acutely infected glial cells showed high co-expression of polymerase and structural proteins (80-85%).
- Persistently infected glial cells exhibited significantly lower polymerase expression (0.6-0.9%) compared to structural proteins.
- Limited polymerase expression was observed in the spinal cord during persistent BeAn infection, contrasting with widespread expression in GDVII-induced acute encephalitis.
Conclusions:
- Restricted viral RNA polymerase expression may be a key factor in establishing and maintaining TMEV persistence.
- Sufficient polymerase expression occurs to elicit a long-term antibody response.
- These findings offer insights into TMEV persistence mechanisms.

