Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47616
Title: Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples
Authors: Atsü N.
Ergin Ç.
Caf N.
Türkoğlu Z.
Döğen A.
İlkit M.
Keywords: acne vulgaris
FastFung agar
fungal infection
Malassezia spp.
seborrheic dermatitis
acne vulgaris
Article
auricle
comparative effectiveness
controlled study
fungus culture
fungus growth
fungus identification
fungus isolation
Gram staining
human
human tissue
major clinical study
Malassezia
Malassezia furfur
Malassezia globosa
Malassezia restricta
Malassezia sloffiae
Malassezia sympodialis
matrix assisted laser desorption ionization time of flight mass spectrometry
nasolabial fold
nonhuman
seborrheic dermatitis
skin
tinea versicolor
acne vulgaris
Malassezia
microbiology
newborn
seborrheic dermatitis
skin
tinea versicolor
agar
Acne Vulgaris
Agar
Dermatitis, Seborrheic
Humans
Infant, Newborn
Malassezia
Skin
Tinea Versicolor
Publisher: John Wiley and Sons Inc
Abstract: Background: Lipophilic basidiomycetous yeasts of the Malassezia genus can cause various skin diseases, such as seborrheic dermatitis, pityriasis versicolor, folliculitis and atopic dermatitis, and even life-threatening fungemia in newborns and immunocompromised individuals. Routine mycological media used in clinical practice do not contain sufficient lipid ingredients required for the growth of Malassezia species. A recently developed medium, FastFung agar, is promising for culturing fastidious fungal species. Methods: In this study, we compared FastFung agar and mDixon agar for culturing Malassezia species from nasolabial fold and retroauricular specimens of 83 healthy individuals and 187 and 57 patients with acne vulgaris and seborrheic dermatitis, respectively. Results: Malassezia species were identified using conventional tests and matrix-assisted laser desorption/ionisation mass spectrometry. In total, 96 of 654 samples (14.6%) contained Malassezia species. The total isolation rate was significantly higher in patients with seborrheic dermatitis (40.4%) than in healthy volunteers (21.7%; p <.05), and the rate of M. furfur isolation was significantly higher for patients with acne vulgaris (13.9%) and seborrheic dermatitis (24.6%) than for healthy individuals (1.5%; p <.05). FastFung agar was superior to mDixon agar in M. furfur isolation (p =.004) but showed similar performance in the case of non-M. furfur species (p >.05). Among cultured Malassezia species, perfect agreement between mDixon agar and FastFung agar was found only for M. globosa (? = 0.90). Conclusion: Our results indicate that FastFung agar favours the growth of Malassezia species and should be useful in clinical mycology laboratories. © 2022 The Authors. Mycoses published by Wiley-VCH GmbH.
URI: https://doi.org/10.1111/myc.13450
https://hdl.handle.net/11499/47616
ISSN: 0933-7407
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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