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The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1953 Feb 28;97(3):315–322. doi: 10.1084/jem.97.3.315

SOME ENERGY RELATIONS IN A HOST-VIRUS SYSTEM

W Wilbur Ackermann 1, R Bernal Johnson 1; With the Technical Assistance of H. Kurtz And L. E. Keith1
PMCID: PMC2136262  PMID: 13052802

Abstract

It was found that DNP (2,4-dinitrophenol) will inhibit completely the propagation of influenza virus in chorioallantoic membrane. This reagent did not permanently alter those metabolic processes required for the synthesis of virus and at the concentrations employed demonstrated no virucidal effects. In minced preparations of chorioallantoic membrane DNP was shown to have a pronounced stimulatory effect upon ATPase (adenosinetriphosphatase). When DNP was used with intact tissues, an excellent correlation was found between the inhibition of viral propagation and the stimulation of respiration and release of phosphate. Concentrations of DNP which permitted a twofold increase in the endogenous respiration of intact membranes allowed little or no viral synthesis. It is concluded that the energy required for viral synthesis derives from the oxidative phosphorylative activity of the host tissue.

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Selected References

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

  1. ACKERMANN W. W., KLERNSCHMIDT E. Concerning the relation of the Krebs cycle to virus propagation. J Biol Chem. 1951 Mar;189(1):421–428. [PubMed] [Google Scholar]
  2. ACKERMANN W. W. The relation of the Krebs cycle to viral synthesis. II. The effect of sodium fluoroacetate on the propagation of influenza virus in mice. J Exp Med. 1951 Jun;93(6):635–642. doi: 10.1084/jem.93.6.635. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. AINSLIE J. D. The growth curve of the Lansing strain of poliomyelitis virus in mice: the effect of sodium monofluoroacetate and methionine sulfoximine on the early phase of growth of the virus. J Exp Med. 1952 Jan;95(1):9–18. doi: 10.1084/jem.95.1.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. JOHNSON R. B., ACKERMANN W. W. A rôle of nuclei in oxidative phosphorylation. J Biol Chem. 1953 Jan;200(1):263–269. [PubMed] [Google Scholar]
  5. JOHNSON R. B., FELDOTT G., LARDY H. A. The mode of action of the antibiotic, usnic acid. Arch Biochem. 1950 Oct;28(3):317–323. [PubMed] [Google Scholar]
  6. KIELLEY W. W., KIELLEY R. K. Myokinase and adenosinetriphosphatase in oxidative phosphorylation. J Biol Chem. 1951 Aug;191(2):485–500. [PubMed] [Google Scholar]
  7. LARDY H. A., WELLMAN H. Oxidative phosphorylations; rôle of inorganic phosphate and acceptor systems in control of metabolic rates. J Biol Chem. 1952 Mar;195(1):215–224. [PubMed] [Google Scholar]
  8. POTTER V. R., LYLE G. G., SCHNEIDER W. C. Oxidative phosphorylation in whole homogenates and in cell particles. J Biol Chem. 1951 May;190(1):293–301. [PubMed] [Google Scholar]
  9. TEPLY L. J. Studies on the cyclophorase system; mechanism of action of 2,4-dinitrophenol. Arch Biochem. 1949 Dec;24(2):383–388. [PubMed] [Google Scholar]
  10. WATANABE T., HIGGINBOTHAM R. D., GEBHARDT L. P. Effect of sodium monofluoroacetate on multiplication of Eastern equine encephalomyelitis virus. Proc Soc Exp Biol Med. 1952 Aug-Sep;80(4):758–761. doi: 10.3181/00379727-80-19754. [DOI] [PubMed] [Google Scholar]
  11. Zinsser H., Schoenbach E. B. STUDIES ON THE PHYSIOLOGICAL CONDITIONS PREVAILING IN TISSUE CULTURES. J Exp Med. 1937 Jul 31;66(2):207–227. doi: 10.1084/jem.66.2.207. [DOI] [PMC free article] [PubMed] [Google Scholar]

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