The urine samples were centrifuged at 3000 rpm for 2 min and emulsified HVS samples in peptone water; 20 ul of the urine deposit or the emulsified HVS were spread on the SDA agar plate using a sterilized glass rod. Urine and the HVS samples were cultured on Sabourauds dextrose agar plates, containing 0.5 mg per 1000 ml chloramphenicol and incubated at 37 o C and examined for its growth at 24, 48 and 72 h. The culture plates were examined for the appearance, size, cream-coloured pastry colonies and morphology of the colonies [19 ].
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