Skip to main content
Springer Nature - PMC COVID-19 Collection logoLink to Springer Nature - PMC COVID-19 Collection
. 1993;132(3):281–289. doi: 10.1007/BF01309539

Virus specificity of the antiviral state induced by IFN gamma correlates with resistance to MHV 3 infection

I G C Mello 1, R C Vassão 1, C A Pereira 1
PMCID: PMC7087277  PMID: 7691047

Summary

A comparative study was carried out to investigate the correlation between the antiviral effect induced in macrophages by IFN gamma and the resistance of A/J and BALB/c mice to an experimental infection of MHV 3, MHV 4, and MHVA 59. Both mouse strains were resistant to intraperitoneal infection with MHV 4 or MHVA 59 and only the A/J mice showed resistance to MHV 3, the BALB/c mice being fully susceptible to this virus infection. Comparable growth kinetics, for all three viruses, were observed in both mouse strains, except for the MHV 3 growth in BALB/c mice, where the virus titre increased to a peak on day 2, remaining high until day 4 when the mice died of acute hepatitis. The IFN gamma titres in the peritoneum of mice preceded and correlated with the virus growth, higher titres being found in MHV 3 infected BALB/c mice. The highest titre was always observed 24 to 48 h after infection. Among viral strains grown in cultured macrophages, higher titres were always observed in cultures infected with MHVA 59, followed by MHV 3 and the lowest those infected with MHV 4. The macrophage activation by IFN gamma-induced a partial restriction of virus growth only in MHV 3 infected A/J mouse macrophages. A virus specificity of the IFN gamma-induced antiviral state was shown to be in direct correlation with the resistance of mice to MHV 3 infection.

Keywords: Hepatitis, Mouse Strain, Viral Strain, Growth Kinetic, High Titre

References

  • 1.Arnheiter H, Baechi T, Haller O. Adult mouse hepatocytes in primary monolayer culture express genetic resistance to mouse hepatitis virus type 3. J Immunol. 1982;129:1275–1281. [PubMed] [Google Scholar]
  • 2.Bang FB, Warwick A. Mouse macrophages as host cells for the mouse hepatitis virus and the genetic basis of their susceptibility. Proc Natl Acad Sci USA. 1960;46:1065–1075. doi: 10.1073/pnas.46.8.1065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Barthold SW. Mouse hepatitis virus biology and epizootiology. In: Bhatt PN, Jacoby RO, Morse HC III, New AE, editors. Viral and mycoplasmal infection of laboratory rodents. Effects of biomedical research. Orlando: Academic Press; 1986. pp. 571–601. [Google Scholar]
  • 4.Cheveer FS, Daniels JB, Pappenheimer AM, Bailey OT. A murine virus (JHM) causing disseminated encephalomyelitis with extensive destruction of myelin I. Isolation and biological properties of the virus. J Exp Med. 1949;90:181–194. doi: 10.1084/jem.90.3.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Damy SB, Vassao RC, Lucchiari MA, Pereira CA, Sant'Anna OA. A comparative study of resistance to MHV 3 infection in genetically homogeneous and heterogeneous mouse populations. Braz J Med Biol Res. 1992;25:1025–1027. [PubMed] [Google Scholar]
  • 6.Dick GNA, Niven JSF, Gledhill AN. A virus related to that causing hepatitis in mice (MHV) Br J Exp Pathol. 1956;37:90–98. [PMC free article] [PubMed] [Google Scholar]
  • 7.Dindzanz VJ, Skamene E, Levy GA. Susceptibility/resistance in mouse hepatitis virus strain 3 and macrophage procoagulant activity are linked and controlled by two non-H-2 linked genes. J Immunol. 1986;137:2355–2362. [PubMed] [Google Scholar]
  • 8.Dupuy JM, Dupuy C, Decarie D. Genetically determined resistance to mouse hepatitis virus type 3 is expressed in hematopoietic donor cells in radiation chimeras. J Immunol. 1984;133:1609–1615. [PubMed] [Google Scholar]
  • 9.Hierholzer JC, Broderson JR, Murphy FA. New strain of mouse hepatitis virus as the cause of lethal enteritis in infant mice. Infect Immun. 1984;24:508–522. doi: 10.1128/iai.24.2.508-522.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Knobler RL, Haspel MV, Oldstone MBA. Mouse hepatitis virus type 4 (JHM strain)-induced fatal central nervous system disease. I. Genetic control and the murine neuron as the susceptible site of disease. J Exp Med. 1981;153:832–843. doi: 10.1084/jem.153.4.832. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Le Prevost C, Levy-Leblond E, Virelizier JL, Dupuy JM. Immunopathology of mouse hepatitis virus type 3 infection. I. Role of humoral and cell-mediated immunity in resistance mechanisms. J Immunol. 1975;114:221–227. [PubMed] [Google Scholar]
  • 12.Levy GA, Leibowitz JL, Edgington TS. Induction of monocyte procoagulant activity by murine hepatitis virus type 3 (MHV 3) parallels disease susceptibility in mice. J Exp Med. 1981;154:1150–1157. doi: 10.1084/jem.154.4.1150. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Lucchiari MA, Pereira CA. A major role of macrophage activation by interferon gamma during mouse hepatitis virus type 3 infection. I. Genetically dependent resistance. Immunobiology. 1989;180:12–22. doi: 10.1016/S0171-2985(89)80026-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Lucchiari MA, Pereira CA. A major role of macrophage activation by interferon gamma during mouse hepatitis virus type 3 infection. II. Age dependent resistance. Immunobiology. 1990;181:31–39. doi: 10.1016/S0171-2985(11)80163-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lucchiari MA, Martin JP, Modolell M, Pereira CA. Acquired immunity of A/J mice to mouse hepatitis virus 3 infection: dependence on interferon gamma synthesis and macrophage sensitivity to interferon gamma. J Gen Virol. 1991;72:1317–1322. doi: 10.1099/0022-1317-72-6-1317. [DOI] [PubMed] [Google Scholar]
  • 16.Martin JP, Koehren F, Rannou JJ, Kirn A. Temperature sensitive mutants of mouse hepatitis virus type 3 (MHV 3): isolation, biochemical, and genetic characterization. Arch Virol. 1988;100:147–160. doi: 10.1007/BF01487679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.McIntosh K. Coronaviruses. In: Fields BN, editor. Virology. New York: Raven Press; 1985. pp. 1323–1330. [Google Scholar]
  • 18.Pereira CA, Steffan AM, Kirn A. Interaction between mouse hepatitis viruses and primary cultures of Kupffer and endothelial liver cells from resistant and susceptible inbred mouse strains. J Gen Virol. 1984;65:1617–1620. doi: 10.1099/0022-1317-65-9-1617. [DOI] [PubMed] [Google Scholar]
  • 19.Pereira CA, Mercier G, Oth D, Dupuy JM. Induction of natural killer cells and interferon during mouse hepatitis virus infection of resistant and susceptible inbred mouse strains. Immunobiology. 1984;166:35–42. doi: 10.1016/S0171-2985(84)80141-2. [DOI] [PubMed] [Google Scholar]
  • 20.Pereira CA, Steffan AM, Koehren F, Kirn A. Inhibition of mouse hepatitis virus type 3 multiplication in activated Kupffer cells. Braz J Med Biol Res. 1985;18:527–531. [PubMed] [Google Scholar]
  • 21.Robb J, Bond CW. Pathogenic murine coronaviruses. I. Characterization of biological behavior in vitro and virus-specific intracellular RNA of strongly neurotropic JHMV and weekly neurotropic A 59 viruses. Virology. 1979;94:352–370. doi: 10.1016/0042-6822(79)90467-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Rowe WP, Hartley JW, Capps WI. Mouse hepatitis virus infection as a highly contagious, prevalent, enteric infection in mice. Proc Soc Exp Biol Med. 1963;112:161–165. doi: 10.3181/00379727-112-27980. [DOI] [PubMed] [Google Scholar]
  • 23.Van der Riet FSJ, Kahn LB. Isolation of a murine hepatitis virus from Swiss mice treated with antilymphocyte serum. Arch Virusforsch. 1973;42:1–8. doi: 10.1007/BF01250502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Virelizier JL, Gresser I. Role of interferon in the pathogenesis of viral diseases of mice as demonstrated by the use of anti-interferon serum. V. Protective role in mouse hepatitis virus type 3 infection of susceptible and resistant strains of mice. J Immunol. 1978;120:1616–1619. [PubMed] [Google Scholar]
  • 25.Virelizier JL. Role of macrophages and interferon in natural resistance to mouse hepatitis virus infections. Curr Top Microbiol Immunol. 1981;92:53–65. doi: 10.1007/978-3-642-68069-4_4. [DOI] [PubMed] [Google Scholar]
  • 26.Wege H, Siddell S, Ter Meulen V. The biology and pathogenesis of coronaviruses. Curr Top Microbiol Immunol. 1982;99:165–200. doi: 10.1007/978-3-642-68528-6_5. [DOI] [PubMed] [Google Scholar]
  • 27.Williams RK, Jiang GS, Holmes KV. Receptor for mouse hepatitis virus is a member of the carcinoembryonic antigen family of glycoproteins. Proc Natl Acad Sci USA. 1991;88:5533–5536. doi: 10.1073/pnas.88.13.5533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Yokomori K, Lai MMC. The receptor for mouse hepatitis virus in the resistant mouse strain SJL is functional: Implications for the requirement of a second factor for viral infection. J Virol. 1992;66:6931–6938. doi: 10.1128/jvi.66.12.6931-6938.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Archives of Virology are provided here courtesy of Nature Publishing Group

RESOURCES