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. 1977 Aug;17(2):268–273. doi: 10.1128/iai.17.2.268-273.1977

Genetics of macrophage-controlled resistance to hepatitis induced by herpes simplex virus type 2 in mice.

S C Mogensen
PMCID: PMC421112  PMID: 197015

Abstract

The genetics of innate resistance of mice to hepatitis induced by herpes simplex virus type 2 (HSV-2) was analyzed by crossing resistant male GR to susceptible female BALB/c mice and backcrossing females of this F1 generation to susceptible male BALB/c mice. By scoring of macroscopic liver lesions and virus isolation studies from the liver 4 days after intraperitoneal inoculation of HSV-2, it appeared that the resistance was governed by one X-linked dominant gene or closely linked gene complex, as F1 female mice were resistant and F1 male mice were susceptible and the trait segregated in a ratio close to 1:1 in the backcross mating. A cellular expression in vitro of virus resistance was found in the macrophage population of the mice as measured by differences in the restriction of HSV-2 replication in macrophage cultures prepared from individual mice. In contrast to what was seen in macrophage cultures, virus replicated equally well in embryonic fibroblast cultures from susceptible and resistant strains of mice.

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Selected References

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  1. Allison A. C. Genetic factors in resistance against virus infections. Arch Gesamte Virusforsch. 1965;17(2):280–294. doi: 10.1007/BF01267912. [DOI] [PubMed] [Google Scholar]
  2. BLOOM J. L., FALCONER D. S. A GENE WITH MAJOR EFFECT ON SUSCEPTIBILITY TO INDUCED LUNG TUMORS IN MICE. J Natl Cancer Inst. 1964 Oct;33:607–618. [PubMed] [Google Scholar]
  3. Bang F. B., Warwick A. MOUSE MACROPHAGES AS HOST CELLS FOR THE MOUSE HEPATITIS VIRUS AND THE GENETIC BASIS OF THEIR SUSCEPTIBILITY. Proc Natl Acad Sci U S A. 1960 Aug;46(8):1065–1075. doi: 10.1073/pnas.46.8.1065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CHANG S. S., HILDEMANN W. H. INHERITANCE OF SUSCEPTIBILITY TO POLYOMA VIRUS IN MICE. J Natl Cancer Inst. 1964 Aug;33:303–313. [PubMed] [Google Scholar]
  5. GOODMAN G. T., KOPROWSKI H. Study of the mechanism of innate resistance to virus infection. J Cell Comp Physiol. 1962 Jun;59:333–373. doi: 10.1002/jcp.1030590313. [DOI] [PubMed] [Google Scholar]
  6. Haller O., Arnheiter H., Lindenmann J. Genetically determined resistance to infection by hepatotropic influenza A virus in mice: effect of immunosuppression. Infect Immun. 1976 Mar;13(3):844–854. doi: 10.1128/iai.13.3.844-854.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hirst R. G., Wallace M. E. Inherited resistance to Corynebacterium kutscheri in mice. Infect Immun. 1976 Aug;14(2):475–482. doi: 10.1128/iai.14.2.475-482.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. KANTOCH M., WARWICK A., BANG F. B. The cellular nature of genetic susceptibility to a virus. J Exp Med. 1963 May 1;117:781–798. doi: 10.1084/jem.117.5.781. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LINDENMANN J. INHERITANCE OF RESISTANCE TO INFLUENZA VIRUS IN MICE. Proc Soc Exp Biol Med. 1964 Jun;116:506–509. doi: 10.3181/00379727-116-29292. [DOI] [PubMed] [Google Scholar]
  10. Lopez C. Genetics of natural resistance to herpesvirus infections in mice. Nature. 1975 Nov 13;258(5531):152–153. doi: 10.1038/258152a0. [DOI] [PubMed] [Google Scholar]
  11. Mogensen S. C. Biological conditions influencing the focal necrotic hepatitis test for differentiation between herpes simplex virus types 1 and 2. Acta Pathol Microbiol Scand B. 1976 Jun;84(3):154–158. [PubMed] [Google Scholar]
  12. Mogensen S. C., Teisner B., Andersen H. K. Focal necrotic hepatitis in mice as a biological marker for differentiation of Herpesvirus hominis type 1 and type 2. J Gen Virol. 1974 Oct;25(1):151–155. doi: 10.1099/0022-1317-25-1-151. [DOI] [PubMed] [Google Scholar]
  13. Mogensen S. Role of macrophages in hepatitis induced by Herpes simplex virus types 1 and 2 in mice. Infect Immun. 1977 Mar;15(3):686–691. doi: 10.1128/iai.15.3.686-691.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Oldstone M. B., Dixon F. J., Mitchell G. F., McDevitt H. O. Histocompatibility-linked genetic control of disease susceptibility. Murine lymphocytic choriomeningitis virus infection. J Exp Med. 1973 May 1;137(5):1201–1212. doi: 10.1084/jem.137.5.1201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. ROBERTS J. A. GROWTH OF VIRULENT AND ATTENUATED ECTROMELIA VIRUS IN CULTURED MACROPHAGES FROM NORMAL AND ECTROMELIAIMMUNE MICE. J Immunol. 1964 Jun;92:837–842. [PubMed] [Google Scholar]
  16. SABIN A. B. Genetic, hormonal and age factors in natural resistance to certain viruses. Ann N Y Acad Sci. 1952 Jul 10;54(6):936–944. doi: 10.1111/j.1749-6632.1952.tb39968.x. [DOI] [PubMed] [Google Scholar]
  17. SCHELL K. Studies on the innate resistance of mice to infection with mousepox. II. Route of inoculation and resistance; and some observations on the inheritance of resistance. Aust J Exp Biol Med Sci. 1960 Aug;38:289–299. doi: 10.1038/icb.1960.30. [DOI] [PubMed] [Google Scholar]
  18. SUBAK-SHARPE H. The effect of passage history, route of inoculation, virus strain and host strain on the susceptibility of adult mice to the virus of foot-and-mouth disease. Arch Gesamte Virusforsch. 1961;11:373–399. doi: 10.1007/BF01249593. [DOI] [PubMed] [Google Scholar]
  19. Sabin A. B. Nature of Inherited Resistance to Viruses Affecting the Nervous System. Proc Natl Acad Sci U S A. 1952 Jun;38(6):540–546. doi: 10.1073/pnas.38.6.540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Selgrade M. K., Osborn J. E. Role of macrophages in resistance to murine cytomegalovirus. Infect Immun. 1974 Dec;10(6):1383–1390. doi: 10.1128/iai.10.6.1383-1390.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Yoon J. W., Notkins A. L. Virus-induced diabetes mellitus. VI. Genetically determined host differences in the replicating of encephalomyocarditis virus in pancreatic beta cells. J Exp Med. 1976 May 1;143(5):1170–1185. doi: 10.1084/jem.143.5.1170. [DOI] [PMC free article] [PubMed] [Google Scholar]

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