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Neurovirulence of Six Different Murine Coronavirus JHMV Variants for Rats

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Journal Virus Res
Specialty Microbiology
Date 1991 Jun 1
PMID 1656623
Citations 8
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Abstract

Six variant viruses of the JHMV strain of murine coronavirus with large (cl-2, CNSV, DL and DS) or small (sp-4 and JHM-X) S proteins were compared in terms of their relative neurovirulence in weanling Lewis rats. Inoculation of various doses of the variants revealed that the cl-2 and CNSV were highly virulent and DL and DS were low-virulent, while sp-4 and JHM-X were avirulent. Pathological examination of rats infected with variants cl-2, DL and sp-4 showed that the cl-2 and DL induced severe and mild acute encephalomyelitis, respectively, while no lesions were observed in the central nervous system of rats infected with sp-4. Virus growth and distribution of antigen in rat brains correlated strongly with neurovirulence. These results suggest that S protein plays a role in neurovirulence in rats. In addition, these variant viruses were shown to be useful tools for further analysis of JHMV neurovirulence in animals as well as in cultured cells.

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References
1.
Massa P, Dorries R, Ter Meulen V . Viral particles induce Ia antigen expression on astrocytes. Nature. 1986; 320(6062):543-6. PMC: 7094962. DOI: 10.1038/320543a0. View

2.
Taguchi F, Yamada A, Fujiwara K . Resistance to highly virulent mouse hepatitis virus acquired by mice after low-virulence infection: enhanced antiviral activity of macrophages. Infect Immun. 1980; 29(1):42-9. PMC: 551072. DOI: 10.1128/iai.29.1.42-49.1980. View

3.
Koga M, Wege H, Ter Meulen V . Sequence of murine coronavirus JHM induced neuropathological changes in rats. Neuropathol Appl Neurobiol. 1984; 10(3):173-84. PMC: 7168023. DOI: 10.1111/j.1365-2990.1984.tb00350.x. View

4.
Nagashima K, Wege H, Meyermann R, Ter Meulen V . Demyelinating encephalomyelitis induced by a long-term corona virus infection in rats. A preliminary report. Acta Neuropathol. 1979; 45(3):205-13. PMC: 7086537. DOI: 10.1007/BF00702672. View

5.
Wege H, Winter J, Meyermann R . The peplomer protein E2 of coronavirus JHM as a determinant of neurovirulence: definition of critical epitopes by variant analysis. J Gen Virol. 1988; 69 ( Pt 1):87-98. DOI: 10.1099/0022-1317-69-1-87. View