A new PCR-based technique for the detection of inter- and intraspecifi
c genetic variation has been tested on isolates of the fungal phytopat
hogens Cladosporium fulvum and Pyrenopeziza brassicae. The method is b
ased on the selective PCR amplification of restriction fragments from
digests of genomic DNA. We show that the technique is very efficient a
t detecting polymorphisms, even in species where very little variation
could previously be found by RFLP analysis. 21 primer combinations we
re used on four isolates of P. brassicae, detecting a total of 162 pol
ymorphisms (mean = 4 . 1 polymorphisms per primer combination per pair
of isolates). Four primer combinations were used on eight isolates of
C. fulvum, detecting a total of 32 polymorphisms (mean = 3 . 3 polymo
rphisms per primer combination per pair of isolates). Primer combinati
ons varied in their ability to detect variation, ranging from 0 to 24
polymorphisms between P. brassicae isolates and 0 to 10 polymorphisms
between C. fulvum isolates. AFLP fingerprints were highly reproducible
and have great potential as a tool for evaluating genetic diversity o
f fungal pathogens.