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. 1964 Sep;88(3):702–708. doi: 10.1128/jb.88.3.702-708.1964

COLORADO TICK FEVER VIRUS IN CELL CULTURE I.

Cell-Type Susceptibility and Interaction With L Cells1

Dennis W Trent a,2, L Vernon Scott a
PMCID: PMC277369  PMID: 14208510

Abstract

Trent, Dennis W. (University of Oklahoma School of Medicine, Oklahoma City) and L. Vernon Scott. Colorado tick fever virus in cell culture. I. Cell-type susceptibility and interaction with L cells. J. Bacteriol. 88:702–708. 1964.—Colorado tick fever (CTF) virus was serially propagated in monolayer cultures of L and FL cells. Early passages of virus in FL cells yielded viral titers 104-fold greater than did the corresponding L-cell passages. During L-cell passage number 4, there was a 103-fold increase in the amount of infectious virus produced as compared with virus cultured earlier in this cell line. Viruses from L-cell passages 8 and 12 were identified with specific immune serum to be CTF viruses which were antigenically similar, if not identical, to the mouse-adapted virus. Parallel titrations of mouse-, L cell-, and FL cell-adapted viruses were performed in mice and replicate monolayers of L, FL, HeLa, KB, chick embryo, and cotton rat kidney cells. Cytopathic effects and viral replication were noted in all cultures except HeLa and cotton rat kidney. Cultures of L, FL, and chick embryo cells were as sensitive to infection as were suckling or weanling mice. KB cells were the least susceptible of those cell types examined. In L-cell cultures, 90% of the input virus was adsorbed to the cells during the first 30 min of incubation. The latent period lasted 10 to 12 hr, and was followed by rapid viral synthesis for the next 10 to 24 hr, depending upon the multiplicity of infection. Curves describing exponential increase in cell-associated and cell-released virus were separated by 4 hr. When the maximal total virus titers were reached, 80 to 90% of the virus was released from the cell.

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Selected References

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  1. BANTA J. E. Cultivation of dengue, western equine encephalomyelitis, Japanese encephalitis and West Nile viruses in selected mammalian cell cultures. Am J Hyg. 1958 May;67(3):286–299. doi: 10.1093/oxfordjournals.aje.a119935. [DOI] [PubMed] [Google Scholar]
  2. COLTER J. S. Nucleic acid as the carrier of viral activity. Prog Med Virol. 1958;1:1–35. [PubMed] [Google Scholar]
  3. DULBECCO R., VOGT M. One-step growth curve of Western equine encephalomyelitis virus on chicken embryo cells grown in vitro and analysis of virus yields from single cells. J Exp Med. 1954 Feb;99(2):183–199. doi: 10.1084/jem.99.2.183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DULBECCO R., VOGT M. Plaque formation and isolation of pure lines with poliomyelitis viruses. J Exp Med. 1954 Feb;99(2):167–182. doi: 10.1084/jem.99.2.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. EAGLE H. Amino acid metabolism in mammalian cell cultures. Science. 1959 Aug 21;130(3373):432–437. doi: 10.1126/science.130.3373.432. [DOI] [PubMed] [Google Scholar]
  6. EIRING A. G., SCHER ER W. F. Appearance of persistently cytopathic Eastern and Western encephalitis viruses after "blind" passage in cultures of L mouse fibroblasts. J Immunol. 1961 Jul;87:96–105. [PubMed] [Google Scholar]
  7. GERLOFF R. K., EKLUND C. M. A tissue culture neutralization test for Colorado tick fever antibody and use of the the test for serologic surveys. J Infect Dis. 1959 Mar-Apr;104(2):174–183. doi: 10.1093/infdis/104.2.174. [DOI] [PubMed] [Google Scholar]
  8. HARDY F. M., BROWN A. Growth of Venezuelan equine encephalomyelitis virus in L cells. I. Growth in monolayer cultures. J Bacteriol. 1961 Jan;81:20–27. doi: 10.1128/jb.81.1.20-27.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HARDY F. M. THE GROWTH OF ASIBI STRAIN YELLOW FEVER VIRUS IN TISSUE CULTURES. II. MODIFICATION OF VIRUS AND CELLS. J Infect Dis. 1963 Jul-Aug;113:9–14. doi: 10.1093/infdis/113.1.9. [DOI] [PubMed] [Google Scholar]
  10. HENDERSON J. R. Applications of primary cell cultures in the study of animal viruses. II. Variations in host responses to infection by certain arthropod-borne viruses. Yale J Biol Med. 1961 Apr;33:350–358. [PMC free article] [PubMed] [Google Scholar]
  11. LENNETTE E. H., OTA M. I., HO H., SCHMIDT N. J. Comparative sensitivity of four host systems for the isolation of certain arthropod-borne viruses from mosquitoes. Am J Trop Med Hyg. 1961 Nov;10:897–904. doi: 10.4269/ajtmh.1961.10.897. [DOI] [PubMed] [Google Scholar]
  12. PICKENS E. G., LUOTO L. Tissue culture studies with Colorado tick fever virus. I. Isolation and propagation of virus in KB cultures. J Infect Dis. 1958 Jul-Aug;103(1):102–107. doi: 10.1093/infdis/103.1.102. [DOI] [PubMed] [Google Scholar]
  13. SCHULZE I. T., SCHLESINGER R. W. Plaque assay of dengue and other group B arthropod-borne viruses under methyl cellulose overlay media. Virology. 1963 Jan;19:40–48. doi: 10.1016/0042-6822(63)90022-9. [DOI] [PubMed] [Google Scholar]
  14. WAGNER R. R. Biological studies of interferon. II. Temporal relationships of virus and interferon production by cells infected with Eastern equine encephalomyelitis and influenza viruses. Virology. 1963 Feb;19:215–224. doi: 10.1016/0042-6822(63)90011-4. [DOI] [PubMed] [Google Scholar]

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