Variation within ribosomal DNA. (rDNA) genes of 19 isolates of Pisolithus f
rom different geographic origins and hosts was examined by polymerase chain
reaction (PCR) coupled with restriction fragment length polymorphism (RFLP
) analysis. The primers utilized amplify rDNA regions in a wide range of fu
ngi. One amplified region includes the internal transcribed spacer (ITS), w
hich has a low degree of conservation. The ITS amplification products (640-
750 bp) were digested with a variety of restriction endonucleases. Cluster
analysis based on the restriction fragments grouped the isolates into three
distinct groups: group I contained isolates collected in the northern hemi
sphere, except Pt 1, group II contained those collected in Brazil and group
III contained isolate Pt 1. Additional analysis of other rDNA regions, IGS
, 17 S and 25 S rDNA, resulted in similar groups. The data suggest that the
taxonomy and systematics of this ectomycorrhizal fungus should be revised.