A hexadecyltrimethylammonium bromide (CTAB) method for isolating fungal DNA
from clinical samples, suitable for PCR amplification is described. Yeast
and filamentous fungi DNA from clinical samples was amplified with primers
complementary to the genes coding for rRNA, amplifying a 105 bp fragment an
d internal transcribed spacer primers amplifying fragments between 242 and
622 bp. The level of sensitivity was 10 +/- 5 yeast and 28 Aspergillus fumi
gatus CFU ml(-1) of biological fluid.