Skip to main content
Log in

Japanese encephalitis virus replication: A procedure for the selective isolation and characterization of viral RNA species

  • Published:
Archiv für die gesamte Virusforschung Aims and scope Submit manuscript

Summary

The viral RNA species synthesized in a porcine kidney cell line, PS(Y-15), by Japanese encephalitis virus (JEV) are described. Virus titers on these cells ranged between 106 to 107 p.f.u./ml at the end of 2 to 3 days incubation at 35° C. Actinomycin D (AD) could not be used to unmask JEV RNA synthesis since it inhibited virus replication at concentrations necessary to substantially reduce host cell RNA synthesis. Treatment of cells with 1 μg AD/ml and removal prior to infection permitted good JEV replication, and at the same time strongly suppressed synthesis of 28 S and 18 S cellular ribosomal RNA. The problem of separating viral RNA from non-ribosomal RNA that was still being synthesized by AD pretreated cells was resolved by the isolation of the cytoplasmic membrane fraction of infected cells. RNA extracted from the membranes of infected AD pretreated cells and analyzed for sedimentation characteristics on sucrose gradients has four RNA species not found in uninfected cells.They are: (1) 45 S single stranded RNA believed to be the infectious RNA found in the virion; (2) a 27 S RNA single stranded RNA; (3) a 20 S ribonuclease resistant RNA believed to be double stranded and (4) an 8 S RNA species. The RNA species found in JEV infected cells, except for the 8 S form, have been found in group A arboviruses. The procedure described utilizing AD pretreatment of host cells and the separation of the cellular cytoplasmic fraction may well have value for the study of the biosynthetic events involved in the replication of other animal viruses that are inhibited by AD.

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. Baltimore, D., H. J. Eggers, R. M. Franklin, andI. Tamm: Poliovirus-induced RNA polymerase and effects of virus specific inhibitors on its production. Proc. nat. Acad. Sci. (Wash.)49, 843–849 (1963).

    Google Scholar 

  2. Barry, R. D.: The effects of actinomycin D and ultraviolet irradiation on the production of fowl plague virus. Virology24, 563–569 (1964).

    Google Scholar 

  3. Bases, R. E., andA. S. King: Inhibition of Rauscher murine leukemia virus growth in vitro by actinomycin D. Virology32, 175–183 (1967).

    Google Scholar 

  4. Buck, L. L., andC. J. Pfau: Inhibition of lymphocytic choriomeningitis virus replication by actinomycin D and 6-azauridine. Virology37, 698–701 (1969).

    Google Scholar 

  5. Colon, J. I., andJ. B. Idoine: Factors affecting plaque formation by the infectious ribonucleic acid of the equine encephalitis viruses. J. infect. Dis.114, 61–68 (1964).

    Google Scholar 

  6. Dobos, P., andP. Faulkner: Properties of 42 S and 26 S Sindbis viral ribonucleic acid species. J. Virol.4, 429–438 (1969).

    Google Scholar 

  7. East, J. L., andD. W. Kingsbury: Mumps virus replication in chick embryo lung cells: Properties of RNA in virions and infected cells. J. Virol.8, 161–173 (1971).

    Google Scholar 

  8. Friedman, R. M., H. B. Levy, andW. B. Carter: Replication of Semliki Forest virus: Three forms of viral RNA produced during infection. Proc. nat. Acad. Sci. (Wash.)56, 440–446 (1966).

    Google Scholar 

  9. Girard, M., D. Baltimore, andJ. E. Darnell: The poliovirus replication complex: Site for synthesis of poliovirus RNA. J. molec. Biol.24, 59–74 (1967).

    Google Scholar 

  10. Grado, C., S. Fischer, andG. Contreras: The inhibition by actinomycin D of poliovirus multiplication in Hep 2 cells. Virology27, 623–625 (1965).

    Google Scholar 

  11. Grimley, P. M., I. K. Berezesky, andR. M. Friedman: Cytoplasmic structures associated with an arbovirus infection: Loci of viral ribonucleic acid synthesis. J. Virol.2, 1326–1338 (1968).

    Google Scholar 

  12. Igarashi, A., F. Fukunaga, andK. Fukai: Sedimentation characteristics of Japanese encephalitis virus RNA. Biken J.7, 111–119 (1964).

    Google Scholar 

  13. Inoue, Y. K., andM. A. Yamada: Clonal line of porcine kidney stable cells for assay of Japanese encephalitits virus. J. Bact.87, 1239–1240 (1964).

    Google Scholar 

  14. Leventow, L., andJ. M. Bishop: Comparative aspects of poliovirus replication. J. cell. comp. Physiol.76, 265–272 (1970).

    Google Scholar 

  15. Levin, J. G., andR. M. Friedman: Analysis of arbovirus ribonucleic acid forms by polyacrylamide gel electrophoresis. J. Virol.7, 504–514 (1971).

    Google Scholar 

  16. Loh, P. C., andM. Soergel: Growth characteristics of reovirus type 2: Actino-mycin D and synthesis of viral RNA. Proc. nat. Acad. Sci. (Wash.)54, 857–863 (1965).

    Google Scholar 

  17. Martin, R. G., andB. N. Ames: A method for determining the sedimentation behavior of enzymes: Application to protein mixtures. J. biol. Chem.236, 1372–1379 (1961).

    Google Scholar 

  18. Ota, Z.: Electron microscope study of the development of Japanese B encephalitis virus in porcine kidney stable (PS) cells. Virology25, 372–378 (1965).

    Google Scholar 

  19. Schaffer, F. L., andM. Gordon: Differential inhibitory effects of actinomycin D among strains of poliovirus. J. Bact.91, 2309–2316 (1966).

    Google Scholar 

  20. Schluederber, A., R. C. Handel, andS. Chavanich: Actinomycin D: Renewed RNA synthesis after removal from mammalian cells. Science172, 577–579 (1971).

    Google Scholar 

  21. Stollar, V., T. M. Stevens, andR. W. Schlesinger: Studies on the nature of dengue viruses. II. Characterization of viral RNA and effects of inhibitors of RNA synthesis Virology30, 303–312 (1966).

    Google Scholar 

  22. Stollar, V., R. W. Schlesinger, andT. M. Stevens: Studies on the nature of dengue viruses. III. RNA synthesis in cells infected with type 2 dengue viruses. Virology33, 650–658 (1967).

    Google Scholar 

  23. Trent, D. W., C. C. Swensen, andA. A. Qureshi: Synthesis of Saint Louis encephalitits virus ribonucleic acid in BHK-21/13 cells. J. Virol.3, 385–394 (1969).

    Google Scholar 

  24. Vigier, P., andA. Golde: Effects of actinomycin D and of mitomycin C on the development of Rous sarcoma virus. Virology23, 511–519 (1964).

    Google Scholar 

  25. Yamazaki, S.: Effect of endogenous interferon and actinomycin D on growth of Japanese encephalitis virus in chick embryo cells. Jap. J. Microbiol.12, 171–178 (1968).

    Google Scholar 

  26. Zebovitz, E., andA. Brown: Altered viral ribonucleic acid synthesis by a temperature-sensitive mutant of eastern equine encephalitits virus. J. molec. Biol.50, 185–198 (1970).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work was supported by the Bureau of Medicine and Surgery, Department of the Navy, Project MR 041.05.01-0006B3GJ.

The opinions or assertions contained herein are the private ones of the authors and are not to be construed as official or reflecting the views of the Navy Department or the Naval Service at large.

Postdoctoral Research Associate, National Research Council, supported by the Bureau of Medicine and Surgery, Department of the Navy.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zebovitz, E., Leong, J.K.L. & Doughty, S.C. Japanese encephalitis virus replication: A procedure for the selective isolation and characterization of viral RNA species. Archiv f Virusforschung 38, 319–327 (1972). https://doi.org/10.1007/BF01262822

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01262822

Keywords

Navigation