Age-Dependent Pathogenesis of Murine Gammaherpesvirus 68 Infection of the Central Nervous System

Gammaherpesvirus infection of the central nervous system (CNS) has been linked to various neurological diseases, including meningitis, encephalitis, and multiple sclerosis. However, little is known about the interactions between the virus and the CNS in vitro or in vivo. Murine gammaherpesvirus 68 (...

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Veröffentlicht in:Molecules and cells 2009, 27(1), , pp.105-111
Hauptverfasser: Cho, H.J. (Korea University, Seoul, Republic of Korea), Kim, S.B. (Korea University, Seoul, Republic of Korea), Kwak, S.E. (Hallym University, Chuncheon, Republic of Korea), Kang, T.C. (Hallym University, Chuncheon, Republic of Korea), Kim, H.S. (Hallym University, Chuncheon, Republic of Korea), Kwon, H.J. (Hallym University, Chuncheon, Republic of Korea), Kim, Y.W. (Hallym University, Chuncheon, Republic of Korea), Kim, Y.S. (Hallym University, Chuncheon, Republic of Korea), Choi, E.K. (Ilsong Institute of Life Science, Hallym University, Anyang, Republic of Korea), Song, M.J. (Korea University, Seoul, Republic of Korea), E-mail: moonsong@korea.ac.kr
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Sprache:eng
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Zusammenfassung:Gammaherpesvirus infection of the central nervous system (CNS) has been linked to various neurological diseases, including meningitis, encephalitis, and multiple sclerosis. However, little is known about the interactions between the virus and the CNS in vitro or in vivo. Murine gammaherpesvirus 68 (MHV-68 or γHV-68) is genetically related and biologically similar to human gammaherpesviruses, thereby providing a tractable animal model system in which to study both viral pathogenesis and replication. In the present study, we show the successful infection of cultured neuronal cells, microglia, and astrocytes with MHV-68 to various extents. Upon intracerebroventricular injection of a recombinant virus (MHV-68/LacZ) into 4-5-week-old and 9-10-week-old mice, the 4-5-week-old mice displayed high mortality within 5-7 days, while the majority of the 9-10-week-old mice survived until the end of the experimental period. Until a peak at 3-4 days post-infection, viral DNA replication and gene expression were similar in the brains of both mouse groups, but only the 9-10-week-old mice were able to subdue viral DNA replication and gene expression after 5 days post-infection. Pro-inflammatory cytokine mRNAs of tumor necrosis factor-α, interleukin 1β, and interleukin 6 were highly induced in the brains of the 4-5-week-old mice, suggesting their possible contributions as neurotoxic factors in the age-dependent control of MHV-68 replication of the CNS.
ISSN:1016-8478
0219-1032
DOI:10.1007/s10059-009-0011-5