Skip to main content
Wiley - PMC COVID-19 Collection logoLink to Wiley - PMC COVID-19 Collection
. 2008 May 12;17(6):469–484. doi: 10.1111/j.1365-2990.1991.tb00750.x

Coronavirus induced primary demyelination: indications for the involvement of a humoral immune response

F ZIMPRICH 1, J WINTER 2, H WEGE 2, H LASSMANN 1,3,
PMCID: PMC7194304  PMID: 1666174

Abstract

Coronavirus MHV‐JHM infection of rodents can result in demyelinating encephalomyelitis. We analysed histological changes induced by coronavirus MHV‐JHM infection in Lewis rats. Besides an acute disease (AE), chronic panencephalitis (CPE) and subacute demyelinating encephalomyelitis (SDE) were induced. These disease types were differentiated by the incubation period, the localization of lesions, the type of tissue damage and distribution of virus antigen. In AE and CPE, virus antigen was detected in neurons, astrocytes and oligodendrocytes, whereas in SDE neurons lacked virus antigen. Viral nucleocapsid protein (N) was present in the cytoplasm and the spike protein (S) was displayed on the surface of infected neural cells. However, expression of S protein relative to N protein was severely impaired in SDE lesions. Quantitative analysis of infiltrating inflammatory cells revealed that the number of macrophages and T cells were similar in lesions of AE, CPE and SDE. In contrast to that, SDE lesions contained a significantly higher number of IgG† B cells and plasma cells. In addition active demyelinating SDE lesions displayed an enhanced IgG content and deposits of complement C9. These results indicate that virus induced primary demyelination could be a consequence of antibody mediated cytotoxicity. Furthermore, a reduction in the number of cells producing spike protein in the chronic forms of the disease indicates down‐regulation of this protein, possibly mediated by anti‐S antibodies.

Keywords: coronavirus, MHV‐JHM, spike protein, encephalitis, demyelination, remyelination, humoral immune response

REFERENCES

  1. Beushausen S. & Dales S. (1985) In vivo and in vitro models of demyelinating disease. IX Tropism and differentiation regulate the infectious process of corona viruses in primary explants of the rat CNS. Virology 141, 89–101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Blakemore W.F. (1975) Remyelination by Schwann cells of axons demyelinated by intraspinal injection of 6‐aminonicotinamide in the rat. Journal of Neurocytology 4, 745–757. [DOI] [PubMed] [Google Scholar]
  3. Blakemore W.F. (1978) Observations on remyelination in the rabbit spinal cord following demyelination induced by lysolecithin. Neuropathology and Applied Neurobiology 4, 47–59. [DOI] [PubMed] [Google Scholar]
  4. Blakemore W.F., Crang A.J. & Curtis R. (1986) The interaction of Schwann cells with CNS axons in regions containing normal astrocytes. Acta Neuropathology (Berlin) 71, 295–300. [DOI] [PubMed] [Google Scholar]
  5. Blakemore W.F. & Crang A.J. (1988) Extensive oligodendrocyte remyelination following injection of cultured central nervous system cells into demyelinating lesions in adult central nervous system. Developmental Neuroscience 10, 1–11. [DOI] [PubMed] [Google Scholar]
  6. Buchmeier M.J., Lewicki H.A., Talbot P.J. & Knobler R.L. (1984) Murine Hepatitis Virus‐4 (strain JHM)‐induced neurologic disease is modulated in vivo by monoclonal antibody. Virology 132, 261–270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cheever F.S., Daniels J.B., Pappenheimer A.M. & Bailey O.T. (1949) A murine virus (JHM) causing disseminated encephalomyelitis with extensive destruction of myelin: I. Isolation and biological properties of the virus. Journal of Experimental Medicine 90, 181–194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dal Canto M.C. & Rabinowitz S.G. (1981) Experimental models of virus‐induced demyelination of the central nervous system. Annals of Neurology 11, 109–127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dalziel R.G., Lampert P.W., Talbot P.J. & Buchmeier M.J. (1986) Site‐specific alteration of murine hepatitis virus type 4 peplomer glycoprotein E2 results in reduced neurovirulence. Journal of Virology 59, 463–471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dorries R., Watanabe R., Wege H. & . ter Meulen V. (1986) Murine coronavirus induced encephalomyelitides in rats: analysis of immunoglobulins and virus‐specific antibodies in serum and cerebrospinal fluid. Journal of Neuroimmunology 12, 131–142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dorries R., Watanabe R., Wege H. & ter Meulen V. (1987) Analysis of the intrathecal humoral immune response in Brown Norway (BN) rats, infected with the murine coronavirus JHM. Journal of Neuroimmunology 14, 305–316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Erlich S.S., Matsushima G.K. & Stohlman S.A. (1989) Studies on the mechanism of protection from acute viral encephalomyelitis by delayed‐type hypersensitivity inducer T cell clones. Journal of the Neurological Sciences 90, 203–216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fleming J.O., Trousdale M.D., Brabury J., Stohlman S.A. & Weiner L.P. (1987) Experimental demyelination induced by coronavirus JHM (MHV‐4): molecular identification of a viral determinant of paralytic disease. Microbial Pathogenesis 3, 9–20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Herndon R.M., Griffin D.E., McCormick U. & Weiner L.P. (1975) Mouse hepatitis virus‐induced recurrent demyelination. Archives of Neurology 32, 32–35. [DOI] [PubMed] [Google Scholar]
  15. Koga M., Wege H. & ter Meulen V. (1984) Sequence of murine coronavirus induced neuropathological changes in rats. Neuropathology and Applied Neurobiology 10, 173–184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Körner H., Schliephake A., Winter J., Zimprich F., Lassmann H., Sedgwick J., Siddell S. & Wege H. (1991) Nucleocapsid or spike protein specific CD4† T cells alone protect against coronavirus‐induced encephalomyelitis. Journal of Immunology, in press. [PubMed] [Google Scholar]
  17. Kyuwa S. & Stohlman S.A. (1990) Pathogenesis of a neurotropic murine coronavirus, strain JHM in the central nervous system of mice. Seminars in Virology 1, 273–280. [Google Scholar]
  18. Lampert P.W., Sims J.K. & Kniazeff A.J. (1973) Mechanism of demyelination in JHM virus encephalomyelitis. Acta Neuropathologica (Berlin) 24, 76–85. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Lassmann H., Vass K., Brunner C. & Wisniewski H.M. (1986) Peripheral nervous system lesions in experimental allergic encephalomyelitis. Acta Neuropathologica (Berlin) 69, 193–204. [DOI] [PubMed] [Google Scholar]
  20. Lassmann H., Brunner C., Bradl M. & Linington C. (1988) Experimental allergic encephalomyelitis: The balance between encephalitogenic T lymphocytes and demyelinating antibodies determines size and structure of demyelinated lesions. Acta Neuropathologica (Berlin) 75, 566–576. [DOI] [PubMed] [Google Scholar]
  21. Linington C., Bradl M., Lassmann H., Brunner C. & Vass K. (1988) Augmentation of demyelination in rat acute allergic encephalomyelitis by circulating mouse monoclonal antibodies directed against a myelin/oligodendrocyte glycoprotein. American Journal of Pathology 130, 443–454. [PMC free article] [PubMed] [Google Scholar]
  22. Linington C., Lassmann H., Morgan B.P. & Compston D.A.S. (1989) Immunohistochemical localisation of terminal complement component C9 in experimental allergic encephalomyelitis. Acta Neuropathologica (Berlin) 79, 78–85. [DOI] [PubMed] [Google Scholar]
  23. Ludwin S.K. (1980) Chronic demyelination inhibits remyelination in the central nervous system. Laboratory Investigation 43, 382–387. [PubMed] [Google Scholar]
  24. Massa P.T., Wege H. & ter Meulen V. (1986) Analysis of murine hepatitis virus (JHM strain) tropism toward Lewis rat glial cells in vitro. Type I astrocytes and brain macrophages (microglia) as primary glial cell targets. Laboratory Investigation 55, 318–327. [PubMed] [Google Scholar]
  25. Nagashima K., Wege H., Meyermann R. & ter Meulen V. (1978) Corona virus induced subacute demyelinating encephalomyelitis in rats: a morphological analysis. Acta Neuropathologica (Berlin) 44, 63–70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Nagashima K., Wege H., Meyermann R. & ter Meulen V. (1979) Demyelinating encephalomyelitis induced by a longterm corona virus infection in rats. Acta Neuropathologica (Berlin) 45, 205–213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Oldstone M.B.A. (1989) Viral persistence. Cell 56, 517–520. [DOI] [PubMed] [Google Scholar]
  28. Perlman S. & Ries D. (1987) The astrocyte is a target cell in mice persistently infected with mouse hepatitis virus, strain JHM. Microbial Pathogenesis 3, 309–314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Perlman S., Schelper R., Bolger E. & Ries D. (1987) Late onset, symptomatic, demyelinating encephalomyelitis in mice infected with MHV‐JHM in the presence of maternal antibody. Microbial Pathogenesis 2, 185–194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Sorensen O., Percy D. & Dales D. (1980) In vivo and in vitro models of demyelinating diseases III. JHM virus infection of rats. Archives of Neurology 37, 478–484. [DOI] [PubMed] [Google Scholar]
  31. Sorensen O., Coulter‐Mackie M.B., Puchalski S. & Dales S. (1984) In vivo and in vitro models of demyelinating disease IX. Progression of JHM virus infection in the central nervous system of the rat during overt and asymptomatic phases. Virology 137, 347–357. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Spaan W., Cavanagh D. & Horzinek M.C. (1988) Corona viruses: structure and genome expression. Journal of General Virology 69, 2939–2952. [DOI] [PubMed] [Google Scholar]
  33. Tooze J., Tooze S. & Warren G. (1984) Replication of coronavirus MHV‐A59 in sac‐cells: determination of the first site of budding of progeny virus. European Journal of Cell Biology 33, 281–293. [PubMed] [Google Scholar]
  34. Vass K., Berger M.L., Nowak T.S. Jr., Welch W.J. & Lassmann H. (1989) Induction of stress protein HSP70 in nerve cells after status epilepticus in the rat. Neuroscience Letters 100, 259–264. [DOI] [PubMed] [Google Scholar]
  35. Waksman B.H. & Reingold S.C. (1986) Viral etiology of multiple sclerosis. Where does the truth lie Trends in Neuroscience 9, 338–391. [Google Scholar]
  36. Wang F.I., Stohlman S.A. & Fleming J.O. (1990) Demyelination induced by murine hepatitis virus JHM strain (MHV‐4) is immunological mediated. Journal of Neuroimmunology 30, 31–41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Watanabe R., Wege H. & ter Meulen V. (1983) Adoptive transfer of EAE like lesions from rats with coronavirus induced demyelinating encephalomyelitis. Nature (London) 350, 150–153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Watanabe R., Wege H. & ter Meulen V. (1987) Comparative analysis of coronavirus JHM induced demyelinating encephalomyelitis in Lewis and Brown Norway rats. Laboratory Investigation 57, 375–384. [PubMed] [Google Scholar]
  39. Wege H., Koga M., Watanabe R., Nagashima K. & ter Meulen V. (1983) Neurovirulence of murine coronavirus in JHM temperature sensitive mutants in rats. Infection and Immunity 39, 1316–1324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Wege H., Dömes R. & Wege H. (1984a) Hybridoma antibodies to the murine coronavirus JHM: characterization of epitopes on the peplomer protein (E2). Journal of General Virology 65, 19311942. [DOI] [PubMed] [Google Scholar]
  41. Wege H., Watanabe R. & ter Meulen V. (1984b) Relapsing subacute demyelinating encephalomyelitis in rats in the course of coronavirus JHM infection. Journal of Neuroimmunology 6, 325–336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Wege H., Winter J. & Meyermann R. (1988) The peplomer protein E2 of coronavirus JHM as a determinant of neurovirulence: definition of critical epitopes by variant analysis. Journal of General Virology 69, 87–98. [DOI] [PubMed] [Google Scholar]
  43. Wege H., Winter J., Körner H., Flory E., Zimprich F. & Lassmann H. (1990) Coronavirus induced demyelinating encephalomyelitis in rats: immunopathological aspects of viral persistency In Coronaviruses and their Diseases, Eds. Cavanagh D. and Brown T., pp 637–645. Plenum Press, New York . [DOI] [PubMed] [Google Scholar]
  44. Weiner L.P. (1973) Pathogenesis of demyelination induced by a mouse hepatitis virus (JHM virus). Archives of Neurology 28, 298–303. [DOI] [PubMed] [Google Scholar]
  45. Williamson J.S.P. & Stohlman S.A. (1990) Effective clearance of mouse hepatitis virus from the central nervous system requires both CD4† and CD8† T cells. Journal of Virology 64, 4589–4592. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Neuropathology and Applied Neurobiology are provided here courtesy of Wiley

RESOURCES