Skip to main content
Log in

A new technique for isolating pathogenic fungi from mixed flora inocula

  • Published:
Mycopathologia et mycologia applicata Aims and scope Submit manuscript

Abstract

The development of differential and selective media for the isolation of fungi pathogenic for man is briefly reviewed. A new primary culture technique for medical mycology is presented. This involves the use of an appropriate paper carrier impregnated with suitable concentrations of cycloheximide and chloramphenicol. The carrier, when properly placed on the surface of an agar medium inoculated with a mixed-flora specimen, favors the isolation of a wide spectrum of pathogenic and opportunistic fungi. Evaluation systems for the technique included artificial mixtures of bacteria and fungi, pooled clinical materials artificially seeded with fungi, and routine clinical laboratory specimens. Test fungi were grouped according to a selection pattern based on the extent of their outgrowth within the bacterial inhibition zone (BIZ) established by the carrier on a battery of media. Two main advantages of the antibiotics-impregnated carrier system over the antibiotics-fortified medium system are: (1) the diffusion gradient of cycloheximide allows for the selective outgrowth throughout the BIZ of pathogenic fungi resistant to it, and allows the more susceptible fungal pathogens and “opportunists” to grow out up to their levels of tolerance to the antibiotic within the BIZ; (2) the system is economically advantageous.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Ajello, L. (1957) Cultural methods for human pathogenic fungi.J. Chronic Dis. 5:545–551.

    PubMed  Google Scholar 

  2. Ajello, L. &Getz, M. E. (1954) Recovery of dermatophytes from shoes and a shower stall.J. Invest. Dermat. 22:17–21.

    Google Scholar 

  3. Baxter, M. (1965) The use of ink blue in the identification of dermatophytes.J. Invest. Dermat. 44:23–25.

    Google Scholar 

  4. Baxter, M. &Cooper, J. R. (1964) Ink blue as a pH indicator for certain biological systems.Nature (London) 204:1105–1106.

    PubMed  Google Scholar 

  5. Fisher, J. B. &Kane, J. (1968) Production of chlamydospores byCandida albicans cultivated on dilute oxgall agar.Mycopath. Mycol. Appl. 35:224–229.

    Google Scholar 

  6. Fuentes, C. A., Trespalacios, F., Baquero, G. F. &Aboulafia, R. (1952) Effect of actidione on mold contaminants and human pathogens.Mycologia 44:170–175.

    Google Scholar 

  7. Georg, L. K. (1953) Use of a cycloheximide medium for isolation of dermatophytes from clinical materials.Arch. Dermat. and Syph. 67:355–361.

    Google Scholar 

  8. Georg, L. K., Ajello, L. &Gordon, M. A. (1951) A selective medium for the isolation ofCoccidioides immitis.Science 114:387–389.

    Google Scholar 

  9. Georg, L. K., Ajello, L. &Pappageorge, C. (1954) Use of cycloheximide in the selective isolation of fungi pathogenic to man.J. Lab. and Clin. Med. 44:422–428.

    Google Scholar 

  10. Littman, M. L. (1947) A culture medium for the primary isolation of fungi.Science 106:109–111.

    Google Scholar 

  11. Phillips, G. B. &Hanel, E. (1950) Control of mold contaminants on solid media by the use of actidione.J. Bact. 60:104–105.

    PubMed  Google Scholar 

  12. Rosenthal, S. A., Baer, R. L., Litt, J. Z., Rogachefsky, H. &Furnari, D. (1956) Studies on the dissemination of fungi from the feet of subjects with and without fungous disease of the feet.J. Invest. Dermat. 26:41–47.

    Google Scholar 

  13. Rosenthal, S. A. &Furnari, D. (1957) The use of a cycloheximide-chloramphenicol medium in routine culturing for fungi.J. Invest. Dermat. 28:367–371.

    Google Scholar 

  14. Shapiro, E. M., Mullins, J. F. &Pinkerton, M. E. (1956) Comparison of Littman and cycloheximide mediums for primary isolation of dermatophytes.Am. J. Clin. Path. 26:131–135.

    PubMed  Google Scholar 

  15. Sharvill, D. &Talbot, J. M. (1954) Cycloheximide in the isolation of dermatophytes.Brit. J. Dermat. 66:214–217.

    Google Scholar 

  16. Smith, A. G., Taubert, H. D. &Towns, C. M. (1962) Comparative media studies in the isolation ofCandida albicans from pregnant women.Mycopath. Mycol. Appl. 17:269–280.

    Google Scholar 

  17. Taplin, D. (1965) The use of gentamicin in mycology media.J. Invest. Dermat. 45:549–550.

    Google Scholar 

  18. Taplin, D., Zaias, N., Rebell, G. &Blank, H. (1969) Isolation and recognition of dermatophytes on a new medium (DTM).Arch. Dermat. 99:203–209.

    Google Scholar 

  19. Taschdjian, C. L. (1957) Routine identification ofCandida albicans: current methods and a new medium.Mycologia 49:332–338.

    Google Scholar 

  20. Taubert, H. D. &Smith, A. G. (1960) The clinical use of Taschdjian's medium in the diagnosis of vulvovaginal candidiasis.J. Lab. and Clin. Med. 55:820–828.

    Google Scholar 

  21. Whiffen, A. J. (1948) The production, assay, and antibiotic activity of actidione, an antibiotic fromStreptomyces griseus.J. Bact. 56:283–291.

    Google Scholar 

  22. Wiegand, S. E., Ulrich, J. A. &Winkelmann, R. K. (1968) Diagnosis of superficial pathogenic fungi: use of ink blue agar method.Mayo Clinic Proc. 43:795–802.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Smith, A.G., Rohde, P.A. A new technique for isolating pathogenic fungi from mixed flora inocula. Mycopathologia et Mycologia Applicata 47, 105–120 (1972). https://doi.org/10.1007/BF02126158

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02126158

Keywords

Navigation