2000
DOI: 10.1086/313649
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Molecular Epidemiology of Blastomyces dermatitidis

Abstract: The inhalation of conidia of Blastomyces dermatitidis, a fungus found in soil, causes disease in humans and animals. We studied the genetic diversity of this pathogen by extracting DNA yeasts and analyzing them with a polymerase chain reaction (PCR)-based typing system we developed, which used restriction fragment analysis of amplicons from the regions between the rDNA repeats and allowed us to class isolates into 3 major groups. Strains were further differentiated by use of PCR fingerprinting with 3 different… Show more

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Cited by 71 publications
(51 citation statements)
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“…During investigation of another epidemic, this group again isolated the fungus from environmental sources (66). It is noteworthy that a subsequent study that examined a geographically diverse collection of B. dermatitidis isolates with a typing system based on PCR found that the soil isolates from Eagle River were different from the strains that caused the majority of cases (81). Nevertheless, evidence suggests that the ecological niche for B. dermatitidis is wet earth that has been enriched with animal droppings, rotting wood, and other decaying vegetable matter.…”
Section: Epidemiology and Ecology Of B Dermatitidismentioning
confidence: 99%
“…During investigation of another epidemic, this group again isolated the fungus from environmental sources (66). It is noteworthy that a subsequent study that examined a geographically diverse collection of B. dermatitidis isolates with a typing system based on PCR found that the soil isolates from Eagle River were different from the strains that caused the majority of cases (81). Nevertheless, evidence suggests that the ecological niche for B. dermatitidis is wet earth that has been enriched with animal droppings, rotting wood, and other decaying vegetable matter.…”
Section: Epidemiology and Ecology Of B Dermatitidismentioning
confidence: 99%
“…Alternatively, some isolates were cultured on Sabouraud dextrose agar (SDA) slants at 35°C and the DNA was extracted by initial cell disruption with glass beads (425 to 600 m, acid washed) (Sigma, St. Louis, MO) in a solution of 1 M sorbitol and 125 mM EDTA (45).…”
Section: Isolatesmentioning
confidence: 99%
“…Furthermore, other groups have failed to find genotypic differences between the two strains. More study is required before conclusions may be made on genetic differences between the two strains (11). Clinical differences between the African and North American isolates were noted.…”
Section: Discussionmentioning
confidence: 99%