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Differential growth of MHV(PRI) and MHV(C3H) in genetically resistant C3H mice rendered susceptible by eperythrozoon infection

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Summary

Mice of the C3H strain, which are genetically resistant to mouse hepatitis virus, MHV(PRI), became highly susceptible to that virus when preinfected with the murine blood parasite,Eperythrozoon coccoides (E. coccoides). Peak virus titers and deaths occurred 2 or more days later inE. coccoides-infected C3H mice than those events in genetically susceptible Princeton (PRI) mice. Growth curves and infectivity analyses of progeny virus in cultures of susceptible PRI and resistant C3H cells demonstrated that MHV(PRI) itself multiplied to high titer inE. coccoides- infected C3H mice. Variant virus, MHV(C3H), was also produced, but appeared later in the infection and comprised only a small fraction of the progeny virus. On subsequent passage of progeny virus inE. coccoides-infected C3H mice, MHV(PRI) continued to be produced far in excess of MHV(C3H). In normal (E. coccoides-free) C3H mice, progeny virus caused deaths or lesions indicative of the presence of variant virus, and the latter was recovered at a high titer. The action ofE. coccoides, whereby MHV(PRI) multiplication is initiated in genetically resistant (nonpermissive) C3H cells, could not be reproducedin vitro.

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References

  1. Bang, F. B., andA. Warwick: Mouse macrophages as host cells for the mouse hepatitis virus and the genetic basis of their susceptibility. Proc. nat. Acad. Sci. (Wash.)46, 1065–1075 (1960).

    Google Scholar 

  2. Gallily, R., A. Warwick, andF. B. Bang: Effect of cortisone on genetic resistance to mouse hepatitis virusin vivo andin vitro. Proc. nat. Acad. Sci. (Wash.)51, 1158–1164 (1964).

    Google Scholar 

  3. Gallily, R., A. Warwick, andF. B. Bang: Ontogeny of macrophage resistance to mouse hepatitisin vivo andin vitro. J. exp. Med.125, 537–548 (1967).

    PubMed  Google Scholar 

  4. Glasgow, L. A., andT. Odugbemi: The effect ofEperythrozoon coccoides (EC) on the interferon response of mice. In: Bacteriological Proceedings (71st Annual Meeting of the Amer. Soc. for Microbiol., Minneapolis, 1971), 107. Washington, D.C.: Amer. Soc. Microbiol., 1971.

    Google Scholar 

  5. Gledhill, A. W., andG. W. A. Dick: The nature of mouse hepatitis virus infection in weanling mice. J. Path. Bact.69, 311–320 (1955).

    PubMed  Google Scholar 

  6. Gledhill, A. W.: Quantitative aspects of the enhancing action ofEperythrozoa on the pathogenicity of mouse hepatitis virus. J. gen. Microbiol.15, 292–304 (1956).

    PubMed  Google Scholar 

  7. Gledhill, A. W., D. L. J. Bilbey, andJ. S. F. Niven: Effect of certain murine pathogens on phagocytic activity. Brit. J. exp. Path.46, 433–442 (1965).

    PubMed  Google Scholar 

  8. Hirano, T., andB. H. Ruebner: Studies on the mechanism of destruction of lymphoid tissue in murine hepatitis virus (MHV3) infection. I. Selective prevention of lymphoid necrosis by cortisone and puromycin. Lab. Invest.15, 270–282 (1966).

    PubMed  Google Scholar 

  9. Kantoch, M., A. Warwick, andF. B. Bang: The cellular nature of genetic susceptibility to a virus. J. exp. Med.117, 781–797 (1963).

    Google Scholar 

  10. Lavelle, G. C., andF. B. Bang: Influence of type and concentration of serain vitro on susceptibility of genetically resistant cells to mouse hepatitis virus. J. gen. Virol.12, 233–238 (1971).

    PubMed  Google Scholar 

  11. Lavelle, G. C., andT. J. Starr: Interferon response and age-related resistance of germfree mice to mouse hepatitis virus. J. Reticuloendoth. Soc.5, 422–435 (1968).

    Google Scholar 

  12. Lavelle, G. C., andT. J. Starr: Effect of cortisone on interferon response of germfree mice to mouse hepatitis virus. J. Reticuloendoth. Soc.5, 436–444 (1968).

    Google Scholar 

  13. Lavelle, G. C., andT. J. Starr: Relationship of phagocytic activity to pathogenicity of mouse hepatitis virus as affected by triolein and cortisone. Brit. J. exp. Path.50, 475–480 (1969).

    PubMed  Google Scholar 

  14. Nathanson, N., andG. A. Cole: Immunosuppression and experimental virus infection of the nervous system. In: Advances in Virus Research, Vol. 16, pp. 397–448 (K. M. Smith, M. A. Lauffer, andF. B. Bang, eds.). New York: Academic Press, 1970.

    Google Scholar 

  15. Nelson, J. B.: Acute hepatitis associated with mouse leukemia. I. Pathological features and transmission of the disease. J. exp. Med.96, 293–300 (1952).

    PubMed  Google Scholar 

  16. Reed, L. J., andH. Muench: A simple method of estimating fifty-percent end-points. Amer. J. Hyg.27, 493–497 (1938).

    Google Scholar 

  17. Seamer, J., A. W. Gledhill, J. L. Barlow, andJ. Hotchin: Effect ofEperythrozoon coccoides upon lymphocytic choriomeningitis in mice. J. Immunol.86, 512–515 (1961).

    PubMed  Google Scholar 

  18. Shif, I., andF. B. Bang:In vitro interaction of mouse hepatitis virus and macrophages from genetically resistant mice. I. Adsorption of virus and growth curves. J. exp. Med.131, 843–850 (1970).

    PubMed  Google Scholar 

  19. Shif, I., andF. B. Bang:In vitro interaction of mouse hepatitis virus and macrophages from genetically resistant mice. II. Biological characterization of a variant virus MHV (C3H) isolated from stocks of MHV(PRI). J. exp. Med.131, 851–862 (1970).

    PubMed  Google Scholar 

  20. Starr, T. J., andM. Pollard: Susceptibility of cortisone-treated mice to infection with mouse hepatitis virus. Proc. Soc. exp. Biol. Med. (N.Y.)99, 108–110 (1958).

    Google Scholar 

  21. Vella, P. P., andT. J. Starr: Effect of X-radiation and cortisone on mouse hepatitis virus infection in germfree mice. J. infect. Dis.115, 271–277 (1965).

    PubMed  Google Scholar 

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Lavelle, G.C., Bang, F.B. Differential growth of MHV(PRI) and MHV(C3H) in genetically resistant C3H mice rendered susceptible by eperythrozoon infection. Archiv f Virusforschung 41, 175–184 (1973). https://doi.org/10.1007/BF01252763

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