Abstract
Theiler’s murine encephalomyelitis viruses (TMEV) are enteric pathogens of mice and members of the Picornaviridae family. The nucleotide sequence of TMEV and the predicted amino acid sequences of the TMEV-encoded proteins have been compared with other picornaviruses, and a close relationship exists with encephalomyocarditis virus (EMCV), indicating that the TMEV belong to the cardiovirus subgroup of picornaviruses. However, the type of neurologic involvement the TMEV produce is quite distinct from that of other cardioviruses. Following intracerebral (IC) inoculation, certain TMEV strains produce a unique biphasic central nervous system (CNS) disease in their natural murine host [1,2], characterized by poliomyelitis during the first month post infection, and a chronic, inflammatory demyelinating disorder weeks to months later in surviving animals. Mice infected with tissue culture-adapted TMEV do not develop clinical polio but do develop demyelinating disease after a prolonged (30–60 days) incubation period [3]. The demyelination is related to persistent infection wherein for many months low levels of infectious virus can be recovered from the target organ, the CNS [1,4].
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Lipton, H., Miller, S., Melvold, R., Fujinami, R.S. (1986). Theiler’s Murine Encephalomyelitis Virus (TMEV) Infection in Mice as a Model for Multiple Sclerosis. In: Notkins, A.L., Oldstone, M.B.A. (eds) Concepts in Viral Pathogenesis II. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-4958-0_29
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DOI: https://doi.org/10.1007/978-1-4612-4958-0_29
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