Summary
UV-irradiation of SV 40 was shown to reduce considerably the infectivity, the ability to induce T-antigen, and the induction of DNA synthesis. Oncogenicity, however, was reduced only slightly “in vitro” and “in vivo”. The ability of SV 40 to replicate, to form T-antigen, and to induce DNA synthesis do not seem to be necessary conditions for oncogenic potency “in vitro” or “in vivo”. Several interpretations, as well as the possible implication for vaccine-production, are discussed.
Zusammenfassung
Das SV40-Virus zeigte nach UV-Bestrahlung eine erhebliche Reduktion des Infektionstiter, sowie eine starke Abnahme der Fähigkeit zur T-Antigenbildung und Induktion der DNS-Synthese. Die onkogene Wirksamkeit war dagegen nach UV-Bestrahlung des SV40-Virus nur geringfügig „in vitro“ und „in vivo“ vermindert. Die Fähigkeiten des SV40-Virus zur Replikation, T-Antigenbildung und Induktion der DNS-Synthese scheinen keine unbedingten Voraussetzungen für die onkogene Wirksamkeit „in vitro“ und „in vivo“ darzustellen. Verschiedene Deutungsmöglichkeiten, die dieses Phänomen erklären könnten, werden diskutiert. Auf die mögliche Bedeutung dieser Ergebnisse für die Impfstoffherstellung wird hingewiesen.
Similar content being viewed by others
Literatur
Altstein, A. D., G. I. Deichman, O. F. Sarycheva, N. N. Dodonova, E. M. Tsetlin, andN. N. Vassilieva: Oncogenic and transforming activity of Hydroxylamine-inactivated SV40-Virus. Virology33, 747 (1967).
Basilico, C., andG. DiMayorca: Radiation target size of the lytic and the transforming ability of Polyoma virus. Proc. nat. Acad. Sci. (Wash.)54, 125 (1965).
Benjamin, T. L.: Relative target sizes for the inactivation of the transforming and reproductive abilities of Polyoma virus. Proc. nat. Acad. Sci. (Wash.)54, 121 (1965).
Black, P. H., W. P. Rowe, H. C. Turner, andR. J. Huebner: A specific complement fixing antigen present in SV40 transformed cells. Proc. nat. Acad. Sci. (Wash.)50, 1148 (1963).
Carp, R. I., andR. V. Gilden: The inactivation of Simian virus 40 infectivity and antigen-inducing capacity by ultraviolet light. Virology27, 639 (1965).
—,S. Kit, andJ. L. Melnick: The effect of ultraviolet light on the infectivity and enzym-inducing capacity of Papovavirus SV40. Virology29, 503 (1966).
Casto, B. C.: Effect of ultraviolet irradiation on the transforming and plaque-forming capacity of Simian Adenovirus SA 7. J. Virology2, 641 (1968).
Coppey, J., andR. Wicker: Inactivation by U.V., X-, andγ-radiations of two propreties of SV-40 virus: infectivity and ability to induce T-antigen. Ann. Inst. Pasteur115, 478 (1968).
Defendi, V.: Transformation in vitro of mammalian cells by Polyoma and Simian 40 viruses. Progr. exp. Tumor Res.8, 125 (1966).
—, andF. Jensen: Oncogenicity by DNA tumor viruses: enhancement after ultraviolet and Cobalt-60 radiations. Science157, 703 (1967).
— — andG. Sauer: Analysis of some viral functions related to neoplastic transformation. In: Molecular Biology of Viruses, ed.J. S. Colter. London-New York: Academic Pres 1967.
Dulbecco, R.: Viral carcinogenesis. Proc. 9th Internat. Cancer Congress Tokyo 1967.
Gershon, D., P. Hausen, L. Sachs, andE. Winocour: On the mechanism of Polyoma virus-induced synthesis of cellular DNS. Proc. nat. Acad. Sci. (Wash.)54, 1584 (1965).
Habel, K., andB. E. Eddy: Specificity of resistance to tumor challenge of Polyoma- and SV40-virus immune hamsters. Proc. Soc. exp. Biol. (N.Y.)113, 1 (1963).
Hirt, B.: Selective extraction of Polyoma DNA from infected mouse cell cultures. J. molec. Biol.26, 365 (1967).
Hoggan, D., W. P. Rowe, P. H. Black, andR. H. Huebner: Production o “tumor specific” antigens by oncogenic viruses during acute cytolytic infections. Proc. nat. Acad. Sci. (Wash.)53, 12 (1965).
Koch, M. A., andA. B. Sabin: Specificity of virus induced resistance to transplantation of Polyoma and SV40 tumor in adult hamsters. Proc. Soc. exp. Biol. (N.Y.)113, 4 (1963).
Latarjet, R., R. Cramer, andL. Montagnier: Inactivation by U.V.-, X-, andγ-radiations, of the infecting and transforming capacities of Polyoma virus. Virology33, 104 (1967).
Maass, G., u.N. Seemayer: Untersuchungen über die Vermehrung von SV-40 in Gewebekulturen. Zbl. Bakt., I. Abt. Orig.198, 215 (1965).
Marshall, J. D. E., andCh. W. Smith: Superiority of Fluorescein-isothiocyanate for Fluorescent antibody technic with a modification of its application. Proc. Soc. exp. Biol. (N.Y.)98, 898 (1958).
van der Noordaa, J.: Transformation of rat cells by Adenovirus types 1, 2 and 3. J. gen. Virology3, 303 (1969).
Pope, J. H., andW. P. Rowe: Detection of specific antigen in SV40-transformed cells by immunofluorescence. J. exp. Med.120, 121 (1964).
Rapp, F., J. S. Butel, andJ. L. Melnick: Virus-induced intranuclear antigen in cells transformed by papovavirus. Proc. Soc. exp. Biol. (N.Y).116, 1131 (1964).
—,T. Kitahara, J. S. Butel, andJ. L. Melnick: Synthesis of SV40 tumor antigen during replication of simian papovavirus SV-40. Proc. nat. Acad Sci. (Wash.)52, 1138 (1964).
Sabin, A. B., andM. Koch: Behaviour of SV-40 non-infectious viral genome in hamster tumor cells. Induction of synthesis of infectious virus. Proc. nat. Acad. Sci. (Wash.)50, 407 (1963).
— —: Source of genetic information for specific complement-fixing antigens in SV40 virus-induced tumors. Proc. nat. Acad. Sci. (Wash.)52, 1131 (1964).
Seemayer, N.: Untersuchungen über die onkogene Transformation von Hamsternierenzellen in vitro durch das Simian Virus (SV-) 40. Z. Krebsforsch.71, 186 (1968).
Seemayer, N.: DNA-Synthesis and T-antigen formation during oncogenic transformation of hamster kidney cells by SV-40 in vitro. First Internat. Congress for Virology Helsinki, 14.–20. 7. 1968.
- Untersuchungen über die maligne Umwandlung von Hamsternierenzellen in vitro durch das Simian Virus (SV-) 40. 2. Arbeitstagung der Deutsch. Ges. für Hygiene und Mikrobiologie, Mainz 7.–8. 10. 1968.
- Noch unveröffentlicht.
Wallis, C., andJ. L. Melnick: Cationic inactivation of vacuolating virus (SV-40) in poliovirus suspension. Tex. Rep. Biol. Med.19, 701 (1961).
Author information
Authors and Affiliations
Additional information
Die Untersuchungen wurden mit Unterstützung der Deutschen Forschungsgemeinschaft im Rahmen der Unit „Medizinische Virologie” durchgeführt.
Rights and permissions
About this article
Cite this article
Seemayer, N., Seemayer, G. & Haas, R. Untersuchungen über die onkogene Transformation, Induktion der DNS-Synthese und T-Antigenbildung durch UV-bestrahltes Simian Virus (SV-) 40. Z. med. Mikrobiol. u. Immunol. 155, 123–132 (1969). https://doi.org/10.1007/BF02123856
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF02123856