We examined five clinical isolates formerly classified as Candida fama
ta to clarify their taxonomic position by DNA-DNA reassociation studie
s and several phenotypic features. Four of the five isolates, M 5101,
M 5102, M 5111 and M 5112, produced ascospores after being grown for 1
week on YM agar at 20 degrees C. By the API 20C system, three of the
five isolates were identified as C. famata, and the other two strains
as C. guilliermondii/C. famata. The antigenic patterns of all the isol
ates examined with the Candida Check kit were similar to those of C. g
uilliermondii. Specific antiserum against C. saitoana was obtained by
adsorption. However, none of the clinical isolates tested reacted with
this adsorbed serum. The mol% G + C of the four sporulated isolates r
anged from 35.8 to 37.7 and that of the remaining, non-sporulated, iso
late M 2054 was 43.4. The DNA reassociation value was determined by th
e spectrophotometric method. M 5111 and M 5112 were identified as Deba
ryomyces hansenii var. hansenii, M 5101 and M 5102 as D. hansenii var.
fabryi and M 2054 as C. guilliermondii. The ascospore formation was e
xclusive to the four isolates related to D. hansenii. These findings s
uggest that with the exception of C. guilliermondii the other C. famat
a isolates examined all belong to a single species, D. hansenii.