Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1972 Aug;10(2):171–178. doi: 10.1128/jvi.10.2.171-178.1972

Sensitivity of Ribonucleic Acid and Deoxyribonucleic Acid Viruses to Different Species of Interferon in Cell Cultures

Julius S Youngner 1, Harshad R Thacore 1, Marion E Kelly 1
PMCID: PMC356447  PMID: 4342236

Abstract

Although two deoxyribonucleic acid (DNA) viruses, pseudorabies (PsRV) and vaccinia, are as susceptible as a ribonucleic acid (RNA) virus, vesicular stomatitis (VSV), to interferon when tested in chicken or mouse cells, they are refractory to inhibition in interferon-treated primary rabbit kidney cells and in a continuous line (RK-13) of rabbit kidney cells. Superinfection with VSV of RK-13 cells first infected with PsRV completely blocks the replication of PsRV with no effect on VSV yield. When the same experiment is carried out in RK-13 cells pretreated with 1,000 units of interferon, VSV replication is inhibited, which permits PsRV to replicate normally. These findings demonstrate that in the same cell one virus (PsRV) can be refractory to interferon and a second virus (VSV) can be susceptible. These experiments show that rabbit kidney cell cultures are deficient in the synthesis of resistance factors active against the DNA viruses tested and raise the possibility that separate resistance factors may exist for RNA and DNA viruses. In the case of sequential infection of interferon-treated RK-13 cells with vaccinia and VSV, it was found that not only was vaccinia replication refractory to inhibition by interferon, but also that prior infection with vaccinia was able to partially reverse the effect of the inhibitor on the replication of the VSV used for superinfection. On the basis of these and other data it is postulated that a vaccinia virion component or a replication product of vaccinia virus, or both, enables VSV to escape the inhibiting action of interferoninduced resistance factors.

Full text

PDF
171

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CANTELL K., TOMMILA V. Effect of interferon on experimental vaccinia and herpes-simplex virus infections in rabbits' eyes. Lancet. 1960 Sep 24;2(7152):682–684. doi: 10.1016/s0140-6736(60)91751-7. [DOI] [PubMed] [Google Scholar]
  2. Hallum J. V., Thacore H. R., Youngner J. S. Factors affecting the sensitivity of different viruses to interferon. J Virol. 1970 Aug;6(2):156–162. doi: 10.1128/jvi.6.2.156-162.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Hallum J. V., Younger J. S. Quantitative aspects of inhibition of virus replication by interferon in chick embryo cell cultures. J Bacteriol. 1966 Oct;92(4):1047–1050. doi: 10.1128/jb.92.4.1047-1050.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. NAGANO Y., KOJIMA Y. Inhibition de l'infection vaccinale par un facteur liquide dans le tissu infecté par le virus homologue. C R Seances Soc Biol Fil. 1958;152(11):1627–1629. [PubMed] [Google Scholar]
  5. Oh J. O., Yoneda C. Induction of ocular resistance to vaccinia virus by typhoid vaccine: role of interferon. J Immunol. 1969 Jan;102(1):145–154. [PubMed] [Google Scholar]
  6. Padgett B. L., Walker D. L. Effect of persistent fibroma virus infection on susceptibility of cells to other viruses. J Virol. 1970 Feb;5(2):199–204. doi: 10.1128/jvi.5.2.199-204.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Stewart W. E., 2nd, Scott W. D., Sulkin S. E. Relative sensitivities of viruses to different species of interferon. J Virol. 1969 Aug;4(2):147–153. doi: 10.1128/jvi.4.2.147-153.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Thacore H., Youngner J. S. Cells persistently infected with Newcastle disease virus. II. Ribonucleic acid and protein synthesis in cells infected with mutants isolated from persistently infected L cells. J Virol. 1970 Jul;6(1):42–48. doi: 10.1128/jvi.6.1.42-48.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Tsuchiya Y., Tagaya I. General characteristics of enhanced plague formation by poliovirus in poxvirus-infected cells. J Gen Virol. 1972 Mar;14(3):229–235. doi: 10.1099/0022-1317-14-3-229. [DOI] [PubMed] [Google Scholar]
  10. Tsuchiya Y., Tagaya I. Mechanism of enhanced plaque formation by poliovirus in poxvirus-infected cells. J Gen Virol. 1972 Mar;14(3):237–242. doi: 10.1099/0022-1317-14-3-237. [DOI] [PubMed] [Google Scholar]
  11. WAGNER R. R. Biological studies of interferon. I. Suppression of cellular infection with eastern equine encephalomyelitis virus. Virology. 1961 Mar;13:323–337. doi: 10.1016/0042-6822(61)90152-0. [DOI] [PubMed] [Google Scholar]
  12. WAGNER R. R., LEVEY A. H., SNYDER R. M., RATCLIFF G. A., Jr, HYATT D. F. BIOLOGIC PROPERTIES OF TWO PLAQUE VARIANTS OF VESICULAR STOMATITIS VIRUS (INDIANA SEROTYPE). J Immunol. 1963 Jul;91:112–122. [PubMed] [Google Scholar]
  13. Youngner J. S., Scott A. W., Hallum J. V., Stinebring W. R. Interferon production by inactivated Newcastle disease virus in cell cultures and in mice. J Bacteriol. 1966 Oct;92(4):862–868. doi: 10.1128/jb.92.4.862-868.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES