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. 1970 Sep;68(3):435–446. doi: 10.1017/s0022172400042339

Experimental encephalitis following peripheral inoculation of West Nile virus in mice of different ages

Leslie P Weiner, Gerald A Cole, Neal Nathanson
PMCID: PMC2130816  PMID: 4917916

Abstract

Experimental arbovirus infections of mice provide a convenient model to study factors which determine the occurrence or severity of encephalitis following extraneural infection with certain neurotropic viruses. Varying doses of West Nile or Powassan viruses were inoculated by intraperitoneal or intramuscular routes into mice of varing ages; individual variables were manipulated to influence the outcome of infection. Three patterns of pathogenesis were delineated: (1) Fatal encephalitis, preceded by early viraemia, and invasion of the central nervous system. (2) Inapparent infection, with no detectable viraemia and no evidence of central nervous system invasion. (3) Subclinical encephalitis, usually preceded by trace viraemia, with minimal transient levels of virus in the brain. In this latter type of subclinical infection with a potentially lethal virus, the immune response probably plays an important role in recovery.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Albrecht P. Pathogenesis of neurotropic arbovirus infections. Curr Top Microbiol Immunol. 1968;43:44–91. doi: 10.1007/978-3-642-46118-7_2. [DOI] [PubMed] [Google Scholar]
  2. CLARKE D. H., CASALS J. Techniques for hemagglutination and hemagglutination-inhibition with arthropod-borne viruses. Am J Trop Med Hyg. 1958 Sep;7(5):561–573. doi: 10.4269/ajtmh.1958.7.561. [DOI] [PubMed] [Google Scholar]
  3. Cole C. A., Nathanson N., Rivet H. Viral hemorrhagic encephalopathy of rats. II. Pathogenesis of central nervous system lesions. Am J Epidemiol. 1970 Mar;91(3):339–350. doi: 10.1093/oxfordjournals.aje.a121144. [DOI] [PubMed] [Google Scholar]
  4. Cole G. A., Nathanson N. Potentiation of experimental arbovirus encephalitis by immunosuppressive doses of cyclophosphamide. Nature. 1968 Oct 26;220(5165):399–401. doi: 10.1038/220399a0. [DOI] [PubMed] [Google Scholar]
  5. Cole G. A., Wisseman C. L., Jr Pathogenesis of type 1 dengue virus infection in suckling, weanling and adult mice. 1. The relation of virus replication to interferon and antibody formation. Am J Epidemiol. 1969 Jun;89(6):669–680. doi: 10.1093/oxfordjournals.aje.a120981. [DOI] [PubMed] [Google Scholar]
  6. Doherty P. C. Effect of age on louping-ill encephalitis in the hamster. J Comp Pathol. 1969 Oct;79(4):413–420. doi: 10.1016/0021-9975(69)90060-7. [DOI] [PubMed] [Google Scholar]
  7. Eldadah A. H., Nathanson N. Pathogenesis of West Nile Virus encepahlitis in mice and rats. II. Virus multiplication, evolution of immunofluorescence, and development of histological lesions in the brain. Am J Epidemiol. 1967 Nov;86(3):776–790. doi: 10.1093/oxfordjournals.aje.a120786. [DOI] [PubMed] [Google Scholar]
  8. Eldadah A. H., Nathanson N., Sarsitis R. Pathogenesis of West Nile Virus encephalitis in mice and rats. 1. Influence of age and species on mortality and infection. Am J Epidemiol. 1967 Nov;86(3):765–775. doi: 10.1093/oxfordjournals.aje.a120785. [DOI] [PubMed] [Google Scholar]
  9. GLEISER C. A., GOCHENOUR W. S., Jr, BERGE T. O., TIGERTT W. D. The comparative pathology of experimental Venezuelan equine encephalomyelitis infection in different animal hosts. J Infect Dis. 1962 Jan-Feb;110:80–97. doi: 10.1093/infdis/110.1.80. [DOI] [PubMed] [Google Scholar]
  10. Grossberg S. E., Scherer W. F. The effect of host age, virus dose and route of inoculation on inapparent infection in mice with Japanese encephalitis virus. Proc Soc Exp Biol Med. 1966 Oct;123(1):118–124. doi: 10.3181/00379727-123-31418. [DOI] [PubMed] [Google Scholar]
  11. MIMS C. A. ASPECTS OF THE PATHOGENESIS OF VIRUS DISEASES. Bacteriol Rev. 1964 Mar;28:30–71. doi: 10.1128/br.28.1.30-71.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Postic B., Schleupner C. J., Armstrong J. A., Ho M. Two variants of Sindbis virus which differ in interferon induction and serum clearance. I. The phenomenon. J Infect Dis. 1969 Sep;120(3):339–347. doi: 10.1093/infdis/120.3.339. [DOI] [PubMed] [Google Scholar]
  13. Subrahmanyan T. P., Mims C. A. Fate of intravenously administered interferon and the distribution of interferon during virus infections in mice. Br J Exp Pathol. 1966 Apr;47(2):168–176. [PMC free article] [PubMed] [Google Scholar]
  14. Thind I. S., Price W. H. Recovery from primary infection with Langat E5 virus in normal and cyclophosphamide treated mice: relative roles of virus multiplication, interferon, antibody and serum protective factor. Am J Epidemiol. 1969 May;89(5):593–605. doi: 10.1093/oxfordjournals.aje.a120972. [DOI] [PubMed] [Google Scholar]
  15. Thind I. S., Price W. H. The effect of cyclophosphamide treatment on experimental arbovirus infections. Am J Epidemiol. 1969 Jul;90(1):62–68. doi: 10.1093/oxfordjournals.aje.a121050. [DOI] [PubMed] [Google Scholar]
  16. VAINIO T., GWATKIN R., KOPROWSKI H. Production of interferon by brains of genetically resistant and susceptible mice infected with West Nile virus. Virology. 1961 Jul;14:385–387. doi: 10.1016/0042-6822(61)90328-2. [DOI] [PubMed] [Google Scholar]
  17. Webb H. E., Wight D. G., Wiernik G., Platt G. S., Smith C. E. Langat virus encephalitis in mice. II. The effect of irradiation. J Hyg (Lond) 1968 Sep;66(3):355–364. doi: 10.1017/s002217240004122x. [DOI] [PMC free article] [PubMed] [Google Scholar]

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