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Unsaturated free fatty acids inactivate animal enveloped viruses

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Summary

Unsaturated free fatty acids such as oleic, arachidonic or linoleic at concentrations of 5–25 µg/ml inactivate enveloped viruses such as herpes, influenza, Sendai, Sindbis within minutes of contact. At these concentrations the fatty acids are inocuous to animal host cellsin vitro. Naked viruses, such as polio, SV40 or EMC are not affected by these acids. Saturated stearic acid does not inactivate any viruses at concentrations tested. Though the mode of action of unsaturated fatty acids is not understood, electronmicrographs of enveloped viruses treated by them indicate that the inactivation is associated with disintegration of the virus envelope.

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References

  1. Klenk, H. D., Choppin, P. W.: Lipids of plasma membranes of monkey and hamster kidney cells and of parainfluenza virions grown in these cells. Virology38, 255–268 (1969).

    Google Scholar 

  2. Pfefferkorn, E. R., Hunter, H. S.: The source of the Ribonucleic acid and phospholipid of Sindbis virus. Virology20, 445–456 (1963).

    Google Scholar 

  3. Quigley, J. P., Rifkin, D. B., Reich, R.: Phospholipid composition of Rous sarcoma virus, host cell membranes and other enveloped RNA viruses. Virology46, 106–116 (1971).

    Google Scholar 

  4. Hirschberg, C. B., Robbins, P. W.: The glycolipids and phospholipids of Sindbis virus and their relations of the lipids of the host cell plasma membrane. Virology61, 602–608 (1974).

    Google Scholar 

  5. Shinitzky, M., Inbar, M.: Microviscosity parameters and protein mobility in biological membranes. Biochim. Biophys. Acta433, 133–149 (1976).

    Google Scholar 

  6. Hubbell, W. L., McConnel, H. M.: Molecular motion in spin-labeled phospholipids and membranes. J. Amer. chem. Soc.93, 314–326 (1971).

    Google Scholar 

  7. Shinitzky, M., Inbar, M.: Difference in microviscosity induced by different cholesterol levels in the surface membrane lipid layer of normal lymphocytes and malignant lymphoma cells. J. mol. Biol.85, 603–615 (1974).

    Google Scholar 

  8. Landsberger, F. R., Lenard, J., Paxton, J., Compans, R. W.: Spin labeled electron resonance study on the lipid containing membrane of influenza virus. Proc. Natl. Acad. Sci. U.S.A.68, 2579–2588 (1971).

    Google Scholar 

  9. Landsberger, F. R., Compans, R. W.: Effect of membrane protein on the lipid by layer structure. A spin label electron spin resonance study of vesicular stomatitis virus. Biochemistry15, 2356–2360 (1976).

    Google Scholar 

  10. Barenholz, Y., Moore, N. F., Wagner, R. R.: Enveloped viruses as model membrane systems: microviscosity of vesicular stomatitis virus and host cell membrane. Biochemistry15, 3563–3570 (1976).

    Google Scholar 

  11. Rosenthal, K. S., Yanovich, S., Inbar, M., Strominger, J. L.: Translocation of a hydrocarbon fluorescent probe between Epstein-Barr virus and lymphoid cells. An assay for early events in viral infection. Proc. Natl. Acad. Sci. U.S.A.75, 5076–5080 (1979).

    Google Scholar 

  12. Nicolau, C., Klenk, H. D., Hildebrand, K., Reiman, B., Reiman, A., Bauer H.: Early molecular events in the interaction of enveloped viruses with cells. I. A fluorescence and radioactivity study. Biophys. Struct. Mechanism5, 11–23 (1979).

    Google Scholar 

  13. Chapman, D., Wallach, D. F. H.: Recent physical studies of phospholipids and natural membranes. In:Chapman, D. (ed.), Biological Membranes, 125. London: Academic Press 1968.

    Google Scholar 

  14. Rosenfeld, C., Jasmin, C., Mathe, G., Inbar, M.: Dynamics and composition of cellular membranes and serum lipids in malignant disorders, 63–77. In:Bonadonna, G., Mathe, G., Salmon, S. E. (ed.), Recent results in cancer research, Vol. 67. Berlin-Heidelberg-New York: Springer 1979.

    Google Scholar 

  15. Williams, R. E., Wisnieski, B. J., Rittenhouse, H. G., Fox, C. F.: Utilization of fatty acid supplements by cultured cells. Biochemistry13, 1969–1977 (1974).

    Google Scholar 

  16. Sands, J. A., Reinhardt, A., Auperin, D., Landin, P.: Inhibition of entry of the lipid containing bacteriophage PR4 by fatty acid derivatives. J. Virol.29, 413 to 416 (1979).

    Google Scholar 

  17. Sands, J. A., Landin, P., Auperin, D., Reinhardt, A.: Enveloped virus inactivation by fatty acid derivatives. Antimicrob. Agents and Chemother.15, 134–136 (1979).

    Google Scholar 

  18. Sands, J. A., Auperin, D., Snipes, W.: Extreme sensitivity of enveloped viruses including herpes simplex to long chain unsaturated monoglycerides and alcohols. Antimicrob. Agents and Chemother.15, 67–73 (1979).

    Google Scholar 

  19. Tanford, C.: The hydrophobic effect and the organization of living matter. Science200, 1012–1018 (1978).

    Google Scholar 

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Kohn, A., Gitelman, J. & Inbar, M. Unsaturated free fatty acids inactivate animal enveloped viruses. Archives of Virology 66, 301–307 (1980). https://doi.org/10.1007/BF01320626

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  • DOI: https://doi.org/10.1007/BF01320626

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