pachydermatis growth on lipid-enriched
Sabouraud's dextrose agar, and 3 (6%) of 50 human samples were positive (Figure 1).
Fungal strains were sub-cultured on
Sabouraud's Dextrose agar (Oxoid, UK) and incubated at 28AdegC for 7 days to enhance sporulation.
Comparison of Culture Positivity in Dermatophyte Test Medium (DTM) and
Sabouraud's Dextrose Agar (SDA) with Actidione SDA DTM N % N % Culture Positive 46 92 48 96 Culture Negative 4 8 2 4 Total 50 100 50 100 Table 4.
The samples were cultured on
Sabouraud's dextrose agar and incubated at room temperature.
For confirmation, the biopsy tissue was inoculated into
Sabouraud's dextrose agar and was kept at 25[degrees]C.After 10 days colonies were velvety to moist, initially white and became grayish pink.
Specimens were cultured in
Sabouraud's dextrose agar and brain-heart infusion agar with blood, gentamicin, and chloramphenicol and incubated at 30 [degrees] C.
neoformans isolates were grown on
Sabouraud's dextrose agar at 37[degrees]C for 48 h, a loopful of cells from the culture was mixed with sterile deionized water and centrifuged.
Sabouraud's Dextrose Agar showing Cryptococcus Colony
Fungal cultural isolation and identification was done using modified
Sabouraud's dextrose agar and Sunflower seed agar plates with Chloramphenicol (0.05mg/ml).
Inoculation was carried out on
Sabouraud's dextrose agar (SDA) and incubated at 37[degrees]C for 7 days or more if required.
Total twenty three cases of onychomycosis were purposively enrolled in the study after microbiological confirmation by potassium hydroxide (KOH) smear and culture on
Sabouraud's dextrose agar (SDA).
Swabs were cultured on
Sabouraud's Dextrose Agar and incubated at ambient temperature for one week.