Affiliation:
1. Department of Microbiology1 and
2. Department of Dermatology, School of Medicine, Juntendo University, Bunkyo-ku,2 Tokyo, Japan
3. Department of Immunobiology,3 Meiji Pharmaceutical University, Kiyose, and
Abstract
ABSTRACT
Members of the genus
Malassezia
, lipophilic yeasts, are considered to be one of the exacerbating factors in atopic dermatitis (AD). We examined variation in cutaneous colonization by
Malassezia
species in AD patients and compared it with variation in healthy subjects. Samples were collected by applying transparent dressings to the skin lesions of AD patients. DNA was extracted directly from the dressings and amplified in a specific nested PCR assay.
Malassezia
-specific DNA was detected in all samples obtained from 32 AD patients. In particular,
Malassezia globosa
and
M. restricta
were detected in approximately 90% of the AD patients and
M. furfur
and
M. sympodialis
were detected in approximately 40% of the cases. The detection rate was not dependent on the type of skin lesion. In healthy subjects,
Malassezia
DNA was detected in 78% of the samples, among which
M. globosa
,
M. restricta
, and
M. sympodialis
were detected at frequencies ranging from 44 to 61%, with
M. furfur
at 11%. The diversity of
Malassezia
species found in AD patients was greater (2.7 species detected in each individual) than that found in healthy subjects (1.8 species per individual). Our results suggest that
M. furfur
,
M. globosa
,
M. restricta
, and
M. sympodialis
are common inhabitants of the skin of both AD patients and healthy subjects, while the skin microflora of AD patients shows more diversity than that of healthy subjects. To our knowledge, this is the first report of the use of a nested PCR as an alternative to fungal culture for analysis of the distribution of cutaneous
Malassezia
spp.
Publisher
American Society for Microbiology
Cited by
143 articles.
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