Skip to main content
Log in

Further studies on a vaccinia virus cytotoxin present in infected cell extracts: Identification as surface tubule monomer and possible mode of action

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

Summary

A vaccinia virus-specific cytotoxic protein (3−10×104 daltons) had previously been detected in extracts of infected HeLa cells. In this study the protein has been shown to be a late gene product and a virion component — almost certainly the monomer of the surface tubules of the vaccinia virion. The relationship of this cytotoxin to a number of early vaccinia-induced cytopathic effects was examined: it was not the mediator of vaccinia-induced early cell rounding, did not inhibit protein or RNA synthesis in cell-free systems or intact cells (after uptake-induction by hypertonic MgSO4), or cause the release of β-glucuronidase from a crude preparation of HeLa cell lysosomes. Its possible role in vaccinia-induced cell degeneration, late in infection, is discussed.

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. Allison, A. C., Malluci, L.: Histochemical studies of lysosomes and lysosomal enzymes in virus-infected cell cultures. J. exp. Med.121, 463–475 (1965).

    Google Scholar 

  2. Bablanian, R.: The prevention of early vaccinia-virus-induced cytopathic effects by inhibition of protein synthesis. J. gen. Virol.3, 51–61 (1968).

    Google Scholar 

  3. Bablanian, R.: Studies on the mechanisms of vaccinia virus cytopathic effects: effect of inhibitors of RNA and protein synthesis on early virus-induced cell damage. J. gen. Virol.6, 221–230 (1970).

    Google Scholar 

  4. Bablanian, R.: Structural and functional alterations in cultured cells infected with cytocidal viruses. Prog. med. Virol.19, 48–83 (1975).

    Google Scholar 

  5. Ben-Hamida, F., Chapeville, F., Beaud, G.:In vitro study of vaccinia virusinduced shut-off of host protein synthesis. In:Haenni, A. L., Beaud, G. (eds.),In vitro Transcription and Translation of Viral Genomes. INSERM47, 355–362 (1975).

  6. Cukor, G., Solotorovsky, M., Kuchler, R. J.: Biological activity of heated diphteria toxin. J. Bact.115, 277–283 (1973).

    Google Scholar 

  7. Ichihashi, Y., Dales, S.: Biogenesis of poxviruses: interrelationship between haemagglutinin production and polykaryocytosis. Virology46, 533–543 (1971).

    Google Scholar 

  8. Jungwirth, C., Joklik, W. K.: Studies on early enzymes in HeLa cells infected with vaccinia virus. Virology27, 80–93 (1965).

    Google Scholar 

  9. Lowry, O. H., Rosebrough, N. S., Farr, A. L., Randall, R. J.: Protein measurement with the Folin phenol reagent. J. biol. Chem.193, 265–275 (1951).

    Google Scholar 

  10. McAuslan, B. R.: Control of induced thymidine kinase activity in the poxvirus-infected cell. Virology20, 162–168 (1963).

    Google Scholar 

  11. Orlov, G., Gancheva, T. Z., Kavaklova, L., Vacheva, V.: Method for the purification and concentration of vaccinia virus. Zbl. Bakt. Hyg. I. Abt., Orig. A.222, 174–179 (1972).

    Google Scholar 

  12. Paoletti, E., Rosemond-Hornbeak, H., Moss, B.: Two nucleic acid-dependent nucleoside triphosphate phosphohydrolases from vaccinia virus. Purification and characterisation. J. biol. Chem.249, 3273–3280 (1974).

    Google Scholar 

  13. Rothman, J. E., Lenard, J.: Membrane assymetry. Science195, 743–753 (1977).

    Google Scholar 

  14. Shida, H., Tanabe, K., Matsumoto, S.: Mechanism of virus occlusion into A-type inclusion during poxvirus infection. Virology76, 217–233 (1977).

    Google Scholar 

  15. Stephen, J., Birkbeck, T. H., Woodward, C. G., Wolstenholme, J.: Vaccinia virus cytotoxin(s). Nature (London)250, 236–238 (1974).

    Google Scholar 

  16. Stern, W., Dales, S.: Biogenesis of vaccinia: isolation and characterisation of a surface component that elicits antibody suppressing infectivity and cell-cell fusion. Virology75, 232–241 (1976).

    Google Scholar 

  17. Stern, W., Dales, S.: Biogenesis of vaccinia: relationship of the envelope to virus assembly. Virology75, 242–255 (1976).

    Google Scholar 

  18. Thacore, H., Wolff, D. A.: Activation of isolated lysosomes by poliovirus-infected cell extracts. Nature (London)218, 1063–1064 (1968).

    Google Scholar 

  19. Weber, K., Osborn, M.: The reliability of molecular weight determinations by dodecylsulphate—polyacrylamide gel electrophoresis. J. biol. Chem.244, 4406 to 4412 (1969).

    Google Scholar 

  20. Weber, L. A., Feman, E. R., Baglioni, C.: A cell-free system from HeLa cells active in initiation of protein synthesis. Biochem.14, 5315–5321 (1975).

    Google Scholar 

  21. Wolstenholme, J., Burgoyne, R. D., Stephen, J.: Studies on the MgSO4-induced cytoplasmic uptake of proteins by cells in culture. Exp. Cell Res.104, 377–388 (1977).

    Google Scholar 

  22. Wolstenholme, J., Woodward, C. G., Burgoyne, R. D., Stephen, J.: Vaccinia virus cytotoxin. Arch. Virol.53, 25–37 (1977).

    Google Scholar 

  23. Wu, G. J., Zubay, G.: Prolonged transcription in a cell-free system involving nuclei and cytoplasm. Proc. Nat. Acad. Sci. U.S.A.71, 1803–1807 (1974).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Burgoyne, R.D., Stephen, J. Further studies on a vaccinia virus cytotoxin present in infected cell extracts: Identification as surface tubule monomer and possible mode of action. Archives of Virology 59, 107–119 (1979). https://doi.org/10.1007/BF01317900

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01317900

Keywords

Navigation