The inhalation of conidia of Blastomyces dermatitidis, a fungus found in so
il, causes disease in humans and animals. We studied the genetic diversity
of this pathogen by extracting DNA yeasts and analyzing them with a polymer
ase chain reaction (PCR)-based typing system we developed, which used restr
iction fragment analysis of amplicons from the regions between the rDNA rep
eats and allowed us to class isolates into 3 major groups. Strains were fur
ther differentiated by use of PCR fingerprinting with 3 different primers.
Fifty-nine isolates collected over 35 years from 15 regions (United States,
India, Africa, Canada) were analyzed. Genotypic groups A, B, and C contain
ed 17, 23, and 19 isolates, which were divided into 5, 15, and 12 types, re
spectively, All 16 isolates from North America in group A were from the upp
er midwestern United States or Canada, whereas 0 of 20 isolates from the so
utheastern United States were in group A. Studies of the largest collection
from 1 locale (Eagle River, WI), revealed that the soil isolates studied w
ere not responsible for the majority of cases in this outbreak, as previous
ly proposed, and that >1 strain was present in the environment and in patie
nts, Overall, these results provide a tool for the epidemiological study of
blastomycosis and illuminate the genetic and geographic diversity of this
important pathogen.