Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1970 Feb;1(2):157–163. doi: 10.1128/iai.1.2.157-163.1970

Influence of Enovid on the Cytopathic Action of Staphylococcal Alpha Toxin

William Yotis 1, Zlatko Savov 1
PMCID: PMC415871  PMID: 16557707

Abstract

The effect of the widely employed oral contraceptive steroid, Enovid, on the cytolytic action of the staphylococcal alpha toxin was investigated as an extension of previous studies in which it was shown that steroids were capable of suppressing induced staphylococcal infection in experimental animals. The cytotoxic action of alpha toxin for tissue cultures was evaluated by use of such parameters as total and viable cell counts, glucose and protein determination, and cytopathic effects in the presence and absence of Enovid. To 3-day-old primary rabbit baby kidney tissue cultures a mixture of 20 μg of norethynodrel per ml [17α-ethynyl-hydroxy-5(10)-estren-3-one] and 5 μg of mestranol per ml (17-ethynelestradiol-3-methyl ether) was added; growth of tissue cultures in Eagle medium was continued till the sixth day, and then one tissue cytopathic dose of alpha toxin per ml was added and the subsequent fate of tissue cultures was assayed. Such cultures yielded higher total and viable cell counts, utilized more glucose, and contained more protein than the control cultures. In control cultures, cytopathogenicity appeared on the third day after the addition of alpha toxin, and it was complete in 24 hr, whereas in tissue cultures treated with Enovid cytopathogenicity was significantly reduced. Thus the mixture of synthetic hormones known as Enovid, in pharmacological concentrations, was found capable of reducing the cytopathic action of alpha toxin, but only to a slightly lesser degree than such natural hormone as progesterone.

Full text

PDF
157

Images in this article

Selected References

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

  1. BERNHEIMER A. W., SCHWARTZ L. L. Isolation and composition of staphylococcal alpha toxin. J Gen Microbiol. 1963 Mar;30:455–468. doi: 10.1099/00221287-30-3-455. [DOI] [PubMed] [Google Scholar]
  2. GABLIKS J., SOLOTOROVSKY M. Cell culture reactivity to diphtheria, Staphylococcus, tetanus and Escherichia coli toxins. J Immunol. 1962 Apr;88:505–512. [PubMed] [Google Scholar]
  3. GOSHI K., CLUFF L. E., NORMAN P. S. Studies on the pathogenesis of staphylococcal infection. VI. Mechanism of immunity conferred by anti-alpha hemolysin. Bull Johns Hopkins Hosp. 1963 Jan;112:31–47. [PubMed] [Google Scholar]
  4. Hallanger H. O., Bengtsson S. Studies on the cell toxicity and species specificity of purified staphylococcal toxins. Acta Pathol Microbiol Scand. 1967;70(1):107–119. doi: 10.1111/j.1699-0463.1967.tb01274.x. [DOI] [PubMed] [Google Scholar]
  5. LAWRENCE J. C. Some effects of staphylococcal and streptococcal toxins upon mammalian skin in tissue culture. Br J Exp Pathol. 1959 Feb;40(1):8–14. [PMC free article] [PubMed] [Google Scholar]
  6. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  7. NOGRADY G., BURTON A. L. [The effect of staphylococcal alpha-toxin on chick embryo cells in tissue cultures]. Pathol Biol. 1961 Apr;9:831–833. [PubMed] [Google Scholar]
  8. OYAMA V. I., EAGLE H. Measurement of cell growth in tissue culture with a phenol reagent (folin-ciocalteau). Proc Soc Exp Biol Med. 1956 Feb;91(2):305–307. doi: 10.3181/00379727-91-22245. [DOI] [PubMed] [Google Scholar]
  9. THAL A. P., EGNER W. The site of action of the Staphylococcus alpha toxin. J Exp Med. 1961 Jan 1;113:67–82. doi: 10.1084/jem.113.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. UI H., MUELLER G. C. THE ROLE OF RNA SYNTHESIS IN EARLY ESTROGEN ACTION. Proc Natl Acad Sci U S A. 1963 Aug;50:256–260. doi: 10.1073/pnas.50.2.256. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. WEISSMANN G., DINGLE J. Release of lysosomal protease by ultraviolet irradiation and inhibition by hydrocortisone. Exp Cell Res. 1961 Oct;25:207–210. doi: 10.1016/0014-4827(61)90328-7. [DOI] [PubMed] [Google Scholar]
  12. WEISSMANN G., FELL H. B. The effect of hydrocortisone on the response of fetal rat skin in culture to ultraviolet irradiation. J Exp Med. 1962 Sep 1;116:365–380. doi: 10.1084/jem.116.3.365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. WEISSMANN G., THOMAS L. Studies on lysosomes. II. The effect of cortisone on the release of acid hydrolases from a large granule fraction of rabbit liver induced by an excess of vitamin A. J Clin Invest. 1963 May;42:661–669. doi: 10.1172/JCI104757. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. WILLMER E. N. Steroids and cell surfaces. Biol Rev Camb Philos Soc. 1961 Aug;36:368–398. doi: 10.1111/j.1469-185x.1961.tb01295.x. [DOI] [PubMed] [Google Scholar]
  15. YOUNGNER J. S. Monolayer tissue cultures. I. Preparation and standardization of suspensions of trypsin-dispersed monkey kidney cells. Proc Soc Exp Biol Med. 1954 Feb;85(2):202–205. doi: 10.3181/00379727-85-20830. [DOI] [PubMed] [Google Scholar]
  16. Yotis W. W., Cummings J. M. Alteration in the multiplication of Staphylococcus aureus by enovid. Can J Microbiol. 1969 Mar;15(3):247–252. doi: 10.1139/m69-045. [DOI] [PubMed] [Google Scholar]
  17. Yotis W. W. In vivo and in vitro action of norethindrone on staphylococci. J Bacteriol. 1967 Nov;94(5):1353–1358. doi: 10.1128/jb.94.5.1353-1358.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Yotis W., Fitzgerald T. Responses of staphylococci to androgens. Appl Microbiol. 1968 Oct;16(10):1512–1517. doi: 10.1128/am.16.10.1512-1517.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Yotis W., Waner J. Antimicrobial properties of testosterone and its intermediates. Antonie Van Leeuwenhoek. 1968;34(3):275–286. doi: 10.1007/BF02046449. [DOI] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES