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.
Similar content being viewed by others
References
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).
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).
Gallily, R., A. Warwick, andF. B. Bang: Ontogeny of macrophage resistance to mouse hepatitisin vivo andin vitro. J. exp. Med.125, 537–548 (1967).
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.
Gledhill, A. W., andG. W. A. Dick: The nature of mouse hepatitis virus infection in weanling mice. J. Path. Bact.69, 311–320 (1955).
Gledhill, A. W.: Quantitative aspects of the enhancing action ofEperythrozoa on the pathogenicity of mouse hepatitis virus. J. gen. Microbiol.15, 292–304 (1956).
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).
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).
Kantoch, M., A. Warwick, andF. B. Bang: The cellular nature of genetic susceptibility to a virus. J. exp. Med.117, 781–797 (1963).
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).
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).
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).
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).
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.
Nelson, J. B.: Acute hepatitis associated with mouse leukemia. I. Pathological features and transmission of the disease. J. exp. Med.96, 293–300 (1952).
Reed, L. J., andH. Muench: A simple method of estimating fifty-percent end-points. Amer. J. Hyg.27, 493–497 (1938).
Seamer, J., A. W. Gledhill, J. L. Barlow, andJ. Hotchin: Effect ofEperythrozoon coccoides upon lymphocytic choriomeningitis in mice. J. Immunol.86, 512–515 (1961).
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).
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).
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).
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).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
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
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF01252763