TOC Agar, 500 g

Candida are yeast-like fungus forming normal flora inhabiting the mouth and throat, the intestinal tract and the genital tract. Under certain conditions, they cause life-threatening diseases particularly in immunocompromised patients. Candida albicans is the species most commonly isolated from patients with nearly all forms of candidiasis. Cryptococcus neoformans is often cultured from the urine of patients with disseminated infection. Cryptococcosis is one of the defining diseases associated with AIDS (1). TOC Agar is a multi-purpose medium developed by Fleming et al (2) for the rapid, presumptive identification of C. albicans and C. neoformans . Both species are common clinical isolates that may be presumptively identified by specific morphological characteristics (3-7). C. albicans and C. stellatoides may be presumptively identified on this medium by the formation of germ tubes and chlamydospores (2, 5). A combination of sorbitan monooleate 80 and oxbile promotes their rapid, sequential development. C. neoformans may be identified by the production of a characteristic brown pigment on this medium (2, 5). Caffeic acid is the substrate for phenol oxidase, an enzyme produced only by C. neoformans (2). The subsequent enzymatic reaction produces melanin, which is absorbed by the yeast cell wall resulting in tan to brown pigmentation. For the germ tube test, lightly touch a single colony from TOC Agar with a loop or Pasteur pipette; remove excess inoculum and then emulsify the yeast cells in 0.5 ml of horse or other serum in a small test tube with a loose cotton-wool plug. Failure to achieve a light inoculum inhibits germ-tube formation. Incubate at 37°C in a water bath for 2-4 hours (8). A drop of suspension is then placed on a glass slide and covered with coverslip. Microscopic examination of typical C. albicans reveals thin germ tubes 3 to 4 mm in diameter and up to 20 mm long; unlike pseudohyphae that are not constricted at their point of origin. Storage and Shelf-life: Store below 30°C in tightly closed container and the prepared medium at 2 - 8°C. Use before expiry date on the label. References: 1. Murray P. R., Baron J. H., Pfaller M. A., Jorgensen J. H. and Yolken R. H., (Ed.), 2003, Manual of Clinical Microbiology,8th Ed., American Society for Microbiology, Washington, D.C. 2. Fleming W. H., Hopkins J. M. and Land, 1977, J. Clin. Microbiol., 5:236. 3. Lennette E. H., Balows A., Hausler W. J. and Shadomy H. J.,(Eds.), 1985, Manual of Clinical Microbiology, 4th Ed., ASM, Washington, D.C. 4. Finegold S. M. and Baron E. J., 1986, Bailey and Scotts Diagnostic Microbiology, 7th Ed., The C.V. Mosby Company, St. Louis. 5. MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams and Wilkins, Baltimore. 6. Campbell M. C. and Stewart J. L., 1980, The Medical Mycology Handbook, John Wiley and sons, New York. 7. Ajello L., Georg L. K., Kaplan W. and Kaufman L., 1963, Laboratory Manual for Medical Mycology, DHEW Publication No. 994, US Govt. Printing Office, Washington, D.C. 8. Collee J. G., Fraser A. G., Marmion B. P., Simmons A., (Eds.), Mackie and McCartney, Practical Medical Microbiology, 1996, 14th Edition, Churchill Livingstone.