1887

Abstract

SUMMARY: The paths of phosphate transfer were compared in normal and vesicular stomatitis virus-infected chick embryo cell monolayers during one-step virus growth. Phosphate entered the normal cell via an inorganic pool in reversible equilibrium with external phosphate, and passed to large-molecule phosphate from this pool or from organic acid-soluble phosphate. During the latent and exponential release periods of virus infection there was no detectable slowing or stimulation of the rate of gain of P by acid-soluble inorganic and organic phosphates (AI and AO), lipid phosphate (LP), ribonucleic acid (RNA) and other phosphate fractions until uptake ceased in nearly all fractions about half-way through exponential release. Negligible P or P entered or left deoxyribonucleic acid (DNA) in normal or infected cells in this system. Before and during exponential release there was no detectable lysis of nuclei, mitochondria or microsomes (examined after isolation), and no detectable loss of P from AI, AO, LP, RNA or DNA, except for a late 30–50 % decrease in the P of the sucrose-soluble RNA of disrupted cells. This could be a secondary effect (i.e. onset of cell death) rather than an essential stage of virus growth. Gross lysis was evident in all fractions 20 hr. after infection, with the exception of the acid-soluble inorganic fraction not in reversible equilibrium with the medium.

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/content/journal/micro/10.1099/00221287-17-2-335
1957-10-01
2024-04-19
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References

  1. Cooper P. D. 1957a; Some characteristics of vesicular stomatitis virus growth-curves in tissue culture. J. gen. Microbiol 17:327
    [Google Scholar]
  2. Cooper P. D. 1957b; An osmotic barrier for inorganic phosphate in chick embryo cells and its stability during the latent and release periods of infection by vesicular stomatitis virus. J. gen. Microbiol 17:353
    [Google Scholar]
  3. Davidson J. N., Frazer S. C., Hutchison W. C. 1949; Phosphorus compounds in the cell. 1. Protein-bound phosphorus fractions studied with the aid of radioactive phosphorus. Biochem. J 49:311
    [Google Scholar]
  4. Davidson J. N., Smellie R. M. S. 1952; Phosphorus compounds in the cell. 2. The separation by ionophoresis on paper of the constituent nucleotides of ribonucleic acid. Biochem. J 52:594
    [Google Scholar]
  5. Fiske C. H., Subbarow Y. 1925; The colorimetric determination of phosphorus. J. biol. Chem 66:375
    [Google Scholar]
  6. Hogeboom G. H., Schneider W. C., Striebich M. J. 1953; Localisation and integration of cellular function. Cancer Res 13:617
    [Google Scholar]
  7. Katchman B. J., Fetty W. O. 1955; Phosphorus metabolism in growing cultures of S. cerevisiae. J. Bact 69:607
    [Google Scholar]
  8. Laird A. K., Nygaard O., Ris H., Barton A. D. 1953; Separation of mitochondria into two morphologically and biochemically distinct types. Exp. Cell Res 5:147
    [Google Scholar]
  9. Mitchell P., Moyle J. 1953; Paths of phosphate transfer in M. pyogenes: phosphate turnover in nucleic acids and other fractions. J. gen. Microbiol 9:257
    [Google Scholar]
  10. Novikoff A. B., Podber E., Ryan J., Noe E. 1953; Biochemical heterogeneity of cytoplasmic particles isolated from rat liver homogenates. J. Histochem. Cytochem 1:27
    [Google Scholar]
  11. Sanford K. K., Earle W. R., Evans V. J., Waltz H. K., Shannon J. E. 1951; The measurement of proliferation in tissue culture by enumeration of cell nuclei. J. nat. Cancer Inst 11:773
    [Google Scholar]
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