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Increased resistance of SV40 transformed human amnion cells to poliovirus infection

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Summary

The increased resistance to poliovirus of SV40 transformed human amnion cells compared with primary cells has been shown to involve reduced cytopathic effect (CPE), delayed and reduced production of virus, inefficiency of infectious center formation, and the failure of transformed cell monolayers to support poliovirus plaque formation. At multiplicities of exposure (plaque-forming units/ cell) less than 10, CPE was negligible in the poliovirus infected transformed cell cultures which could be maintained as living cultures yielding poliovirus up to three months. Infectious center formation at different multiplicities showed that both cell types could be infected with single infectious units, but in cultures of transformed cells, the probability of initiating infection was reduced about 25-fold. Resistance was not observed in primary amnion cultures infected with SV40 in the absence of transformation. However, cellular resistance developed as morphologic transformed cells appeared in SV40 infected cultures. Transformed cells maintained resistance when SV40 multiplication in transformed cultures was suppressed with metabolic inhibitors or eliminated by isolating virus-free clones of transformed cells in the presence of SV40 antiserum.

The mechanism of the increased resistance of SV40 transformed human amnion cells to poliovirus infection involves an inefficiency in the initiation of infection. When compared to the highly susceptible untransformed primary cells, no significant differences in the adsorption, penetration or eclipse of poliovirus were demonstrated. There was no detectable interferon production in the transformed cultures either before or after poliovirus infection. Since infection with infectious poliovirus RNA bypassed resistance, it is concluded that the resistance of the SV40 transformed cells results from an inefficiency in the uncoating of poliovirus to infectious RNA.

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References

  1. Crowell, K.: Specific cell-surface alteration by enteroviruses as reflected by viral-attachment interference. J. Bact.91, 198–204 (1966).

    Google Scholar 

  2. Darnell, J.: Adsorption and maturation of poliovirus in singly and multiply infected HeLa cells. J. exp. Med.107, 633–641 (1958).

    Google Scholar 

  3. Darnell, J., andT. Sawyer: The basis for variation in susceptibility to polio-virus in HeLa cells. Virology11, 665–675 (1960).

    Google Scholar 

  4. Diderholm, H.: Production of interferon by monkey kidney cells infected with simian virus 40. Arch. ges. Virusforsch.14, 39–44 (1964).

    Google Scholar 

  5. Diderholm, H.: Transformation of bovine cellsin vitro by polyoma virus, and the properties of the transformed cells. Proc. Soc. exp. Biol. (N.Y.)124, 1197–1201 (1967).

    Google Scholar 

  6. Diderholm, H., andZ. Dinter: A line of polyoma-transformed BHK 21 cells insusceptible to foot-and-mouth-disease virus. Virology26, 369–372 (1965).

    Google Scholar 

  7. Dubreuil, R., G. Lussier, V. Pavilanis, P. Marois etE. Di Franco: Pouvoir oncogène, sensibilité virale et caractères cytogénétiques de lignées cellulaires de hamster transformées par le virus SV40. Rev. Canad. Biol.23, 303–322 (1964).

    Google Scholar 

  8. Dulbecco, R., andM. Vogt: Plaque formation and isolation of pure lines with poliomyelitis viruses. J. exp. Med.99, 167–182 (1954).

    Google Scholar 

  9. Fenwick, M., andP. Cooper: Early interaction between poliovirus and ERK cells: Some observations on the nature and significance of the rejected particles. Virology18, 212–223 (1962).

    Google Scholar 

  10. Fenyves, A., andZ. Ciobanu: Transformation induced by SV40 in various types of mammalian cell cultures. I. Transformation in cultures of human embryonic cells. Arch. Roum. Path. exp. Microbiol.25, 881–892 (1966).

    Google Scholar 

  11. Fogh, J.: Latent period in monkey kidney and HeLa cell monolayer cultures infected with poliomyelitis virus. Proc. Soc. exp. Biol. (N.Y.)89, 494–497 (1955).

    Google Scholar 

  12. Fogh, J.: Transformation of human amnion cells with simian virus 40. Proc. Amer. Ass. Cancer Res.7, 21 (1966).

    Google Scholar 

  13. Fogh, J., andR. Lund: Plaque formation of poliomyelitis virus on human amnion cell cultures. Proc. Soc. exp. Biol. (N.Y.)90, 80–82 (1955).

    Google Scholar 

  14. Fogh, J., andR. Lund: Continuous cultivation of epithelial cell strain FL from human amniotic membrane. Proc. Soc. exp. Biol. (N.Y.)94, 532–537 (1957).

    Google Scholar 

  15. Fogh, J., L.Ramos, and H.Fogh: Transformation of primary human amnion cells with simian virus 40 (in press) (1969).

  16. Girardi, A.: Host-virus relationships in virus-induced tumors and transformed cells. Cancer Res.26, 1185–1188 (1966).

    Google Scholar 

  17. Haas, R., undG. Maass: Die Wirkung von 5-Jod-2′-desoxyuridin auf die Vermehrung von SV40 in Gewebekulturen. Arch. ges. Virusforsch.14, 567–582 (1964).

    Google Scholar 

  18. Hahn, E., III, andJ. Fogh: Concurrent growth of cells from different human amnions. Exp. Cell Res.39, 453–463 (1965).

    Google Scholar 

  19. Hahn, E., andJ. Fogh: Poliovirus resistance of SV40 transformed human amnion cells. Fed. Proc.27, 582 (1968).

    Google Scholar 

  20. Holland, J.: Receptor affinities as major determinants of enterovirus tissue tropisms in humans. Virology15, 312–326 (1961).

    Google Scholar 

  21. Hsiung, G.-D., andW. Gaylord: The vacuolating virus of monkeys. I. Isolation, growth characteristics, and inclusion body formation. J. exp. Med.114, 975–986 (1961).

    Google Scholar 

  22. Jensen, F., A. Girardi, R. Gilden, andH. Koprowski: Infection of human and simian tissue cultures with Rous sarcoma virus. Proc. nat. Acad. Sci. (Wash.)52, 53–59 (1964).

    Google Scholar 

  23. Joklik, W., andJ. Darnell: The adsorption and early fate of purified poliovirus in HeLa cells. Virology13, 439–447 (1961).

    Google Scholar 

  24. Le Bouvier, G.: Interference and cell protection by poliomyelitis virus in tissue culture. Nature (Lond.)174, 649–650 (1954).

    Google Scholar 

  25. Ledinko, N., andJ. Melnick: Interference between poliomyelitis viruses in tissue culture. J. exp. Med.100, 247–268 (1954).

    Google Scholar 

  26. Mandel, B.: The relationship between penetration und uncoating of poliovirus in HeLa cells. Virology31, 702–712 (1967).

    Google Scholar 

  27. McCoy, T., M. Maxwell, andP. Kruse: Amino acid requirements of the Novikoff hepatoma in vitro. Proc. Soc. exp. Biol. (N.Y.)100, 115–118 (1959).

    Google Scholar 

  28. Melnick, J., andF. Rapp: The use of antiviral compounds in analyzing the sequential steps in the replication of SV40 papovavirus. Ann. N.Y. Acad. Sci.130, 291–309 (1965).

    Google Scholar 

  29. Pasca, S.: Poliovirus-carrying lines of HeLa cells: Their establishment and sensitivity to viruses. Acta microbiol.8, 329–332 (1961).

    Google Scholar 

  30. Pohjanpelto, P., andP. Cooper: Interference between polioviruses induced by strains that cannot multiply. Virology25, 350–357 (1965).

    Google Scholar 

  31. Puck, T., S. Cieciura, andH. Fisher: Clonal growthin vitro of human cells with fibroblastic morphology. Comparison of growth and genetic characteristics of single epithelioid and fibroblast-like cells from a variety of human organs. J. exp. Med.106, 145–158 (1957).

    Google Scholar 

  32. Rubin, H.: The nature of a virus-induced cellular resistance to Rous sarcoma virus. Virology13, 200–206 (1961).

    Google Scholar 

  33. Sabin, A.: Noncytopathogenetic variants of poliomyelitis viruses and resistance to superinfection in tissue culture. Science120, 357 (1954).

    Google Scholar 

  34. Shein, H., J. Enders, andJ. Levinthal: Transformation induced by simian virus 40 in human renal cell cultures. II. Cell-virus relationships. Proc. nat. Acad. Sci. (Wash.)48, 1350–1357 (1962).

    Google Scholar 

  35. Steck, F., andH. Rubin: The mechanism of interference between an avian leukosis virus and Rous sarcoma virus. II. Early steps of infection by RSV of cells under conditions of interference. Virology29, 642–653 (1966).

    Google Scholar 

  36. Strohl, W., H. Rouse, andR. Schlesinger: Properties of cells derived from adenovirus-induced hamster tumors by long-termin vitro cultivation. II. Nature of restricted response to type 2 adenovirus. Virology28, 645–658 (1966).

    Google Scholar 

  37. Noordaa, J. van der, J. Enders, andG. Diamandopoulos: Increased resistance to herpes simplex virus of hamster and human cells transformed by SV40. Proc. Soc. exp. Biol. (N.Y.)122, 915–920 (1966).

    Google Scholar 

  38. Vogt, M., andR. Dulbecco: Properties of HeLa cell cultures with increased resistance to poliomyelitis virus. Virology5, 425–434 (1958).

    Google Scholar 

  39. Wallis, C., andJ. Melnick: Magnesium chloride enhancement of cell susceptibility to poliovirus. Virology16, 122–132 (1962).

    Google Scholar 

  40. Zitcer, E., J. Fogh, andT. Dunnebacke: Human amnion cells for large scale production of poliovirus. Science122, 30–31 (1955).

    Google Scholar 

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This investigation was supported in part by NCl Research Grant CA-08748. Part of thesis submitted byEdwin Hahn to Cornell Graduate School of Medical Sciences, Cornell University, New York, New York, for the degree of Doctor of Philosophy.

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Hahn, E., Fogh, J. Increased resistance of SV40 transformed human amnion cells to poliovirus infection. Archiv f Virusforschung 29, 343–360 (1970). https://doi.org/10.1007/BF01249889

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