- The yeast-like colonies seen growing on the blood agar surface in the image below are lipid-dependent and grow only where olive oil had been applied. This is characteristic of the yeast-like organism, Malassezia furfur, which causes a superficial skin infection known as tinea versicolor.
- The lower image is a lactophenol blue mount made from a portion of the colony seen on the blood agar plate.
- Clinical material: Skin scrapings from patients with superficial lesions, blood and indwelling catheter tips from patients with suspected fungaemia.
- Direct Microscopy: Skin scrapings taken from patients with Pityriasis versicolor stain rapidly when mounted in 10% KOH, glycerol and Parker ink solution and show characteristic clusters of thick-walled round, budding yeast-like cells and short angular hyphal forms up to 8um in diameter (ave. 4um diam.). These microscopic features are diagnostic for Malassezia furfur and culture preparations are usually not necessary.
Microscopic Characteristics:
- Reproductive cell size is about 5 micrometers, with cells shaped like medicine capsules or sometimes bowling pins. Each produces a single phialoconidium followed by successive budding at a single location. Hyphae, very rarely produced in culture, are approximately 2 – 3 micrometers wide and short in length.
- In direct examination of a smear of infected tissue, hyphae are septate and hyaline usually not branched. Conidia resemble budding yeast cells and are approximately 3 micrometers in diameter. Together the hyphae and conidia are said to look like ‘spaghetti and meatballs.
Macroscopic Characteristics:
- Slow growing colonies, appearing at temperatures of 35-37ºC. Colonies begin shiny and white to cream later becoming dull and beige, resembling bacteria-like colonies. Growth takes around one to two weeks on modified SDA which must be supplemented with fatty acids (usually done by covering medium with a thin layer of olive oil).
- Malassezia species, M. furfur and M.pachydermatis, may also cause catheter related sepsis in patients receiving intravenous lipids.