Skip to main content

Advertisement

Log in

Biochemical transformation of mouse cells by herpes simplex virus types 1 and 2: Comparison of different methods for inactivation of viruses

  • Original Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

Comparison of methods to inactivate lytic properties of herpes simplex viruses revealed that ultraviolet irradiation, photodynamic procedures, and heat all destroyed infectivity effectively. Ability to biochemically transform thymidine kinase deficient cells to an enzyme positive phenotype was retained after limited exposure to heat or ultraviolet light but appeared to be destroyed by photodynamic methods employing neutral red. Exposure to 56°C quickly and effectively destroyed transforming activity with lower temperatures being less effective. The most reproducible transforming assays were obtained following inactivation by ultraviolet light. Cell cultures developed by this procedure were virus-free but retained ability to synthesize virus-specific antigens.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Albrecht, T., St. Jeor, S. C., Funk, F. D., Rapp, F.: Multiplicity reactivation of human cytomegalovirus inactivated by ultraviolet light. Int. J. Radiat. Biol.26, 445–454 (1974).

    Google Scholar 

  2. Darai, G., Munk, K.: Neoplastic transformation of rat embryo cells with herpes simplex virus. Int. J. Cancer18, 469–481 (1976).

    Google Scholar 

  3. Darai, G., Braun, R., Flügel, R. M., Munk, K.: Malignant transformation of rat embryo fibroblasts by herpes simplex virus types 1 and 2 at suboptimal temperature. Nature265, 744–746 (1977).

    Google Scholar 

  4. Davidson, R. L., Adelstein, S. J., Oman, M. N.: Herpes simplex virus as a source of thymidine kinase for thymidine kinase-deficient mouse cells: suppression and reactivation of the viral enzyme. Proc. Nat. Acad. Sci.70, 1912–1916 (1973).

    Google Scholar 

  5. Duff, R., Rapp, F.: Properties of hamster embryo fibroblasts transformedin vitro after exposure to ultraviolet-irradiated herpes simplex virus type 2. J. Virol.8, 469–477 (1971).

    Google Scholar 

  6. George, J., Devoret, R., Radman, M.: Indirect ultraviolet-reactivation of phage lambda. Proc. Nat. Acad. Sci. U.S.A.71, 144–147 (1974).

    Google Scholar 

  7. Howett, M. K., Miller, R. L., Rapp, F.: Herpesvirus transformation: inability of infectious virus to mediate transformation in the presence of inactivated virus. (Manuscript in preparation.)

  8. Lin, S., Munyon, W.: Expression of the viral thymidine kinase gene in herpes simplex virus-transformed L cells. J. Virol.14, 1199–1208 (1974).

    Google Scholar 

  9. Littlefield, J. W.: Studies on thymidine kinase in cultured mouse fibroblasts. Biochim. biophys. Acta95, 14–22 (1965).

    Google Scholar 

  10. Lytle, C. D.: Host-cell reactivation in mammalian cells. I. Survival of ultraviolet-irradiated herpes virus in different cell lines. Int. J. Radiat. Biol.19, 329 to 337 (1971).

    Google Scholar 

  11. Macnab, J. C. M.: Transformation of rat embryo cells by temperature-sensitive mutants of herpes simplex virus. J. gen. Virol.24, 143–153 (1974).

    Google Scholar 

  12. Macpherson, I., Montagnier, L.: Agar suspension culture for the selective assay of cells transformed by polyoma virus. Virology23, 291–294 (1964).

    Google Scholar 

  13. Munyon, W., Kraiselburd, E., Davis, D., Mann, J.: Transfer of thymidine kinase to thymidine kinaseless L cells by infection with ultraviolet-irradiated herpes simplex virus. J. Virol.7, 813–820 (1971).

    Google Scholar 

  14. Plummer, G., Lewis, B.: Thermoinactivation of herpes simplex virus and cytomegalovirus. J. Bacteriol.89, 671–674 (1965).

    Google Scholar 

  15. Pope, J. H., Rowe, W. P.: Detection of specific antigen in SV 40-transformed cells by immunofluorescence. J. exp. Med.120, 121–128 (1964).

    Google Scholar 

  16. Rapp, F.: Variants of herpes simplex virus: isolation, characterization, and factors influencing plaque formation. J. Bacteriol.86, 985–991 (1963).

    Google Scholar 

  17. Rapp, F., Buss, E. R.: Comparison of herpes simplex isolates using a quantitative selection assay for transformation. Intervirology6, 72–82 (1975/76).

    Google Scholar 

  18. Rapp, F., Li, J. L. H., Jerkofsky, M.: Transformation of mammalian cells by DNA-containing viruses following photodynamic inactivation. Virology55, 339–346 (1973).

    Google Scholar 

  19. Ross, L. J. N., Cameron, K. R., Wildy, P.: Ultraviolet irradiation of herpes simplex virus: reactivation processes and delay in virus multiplication. J. gen. Virol.16, 299–311 (1972).

    Google Scholar 

  20. Ross, L. J. N., Wildy, P., Cameron, K. R.: Formation of small plaques by herpes viruses irradiated with ultraviolet light. Virology45, 808–812 (1971).

    Google Scholar 

  21. Roubal, J., Vonka, V.: Multiplicity reactivation in UV-irradiated herpes simplex type 1 virus. Intervirology1, 73–79 (1973).

    Google Scholar 

  22. Wallis, C., Scheiris, C., Melnick, J. L.: Photodynamically inactivated vaccines prepared by growing viruses in cells containing neutral red. J. Immunol.99, 1134–1139 (1967).

    Google Scholar 

  23. Wallis, C., Melnick, J.: Thermostabilization and thermosensitization of herpesvirus. J. Bacteriol.90, 1632–1637 (1965).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

With 7 Figures

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rapp, F., Turner, N. Biochemical transformation of mouse cells by herpes simplex virus types 1 and 2: Comparison of different methods for inactivation of viruses. Archives of Virology 56, 77–87 (1978). https://doi.org/10.1007/BF01317284

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01317284

Keywords

Navigation