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Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples

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...

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Autores principales: Atsü, Nilhan, Ergin, Çağrı, Caf, Nazlı, Türkoğlu, Zafer, Döğen, Aylin, İlkit, Macit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321000/
https://www.ncbi.nlm.nih.gov/pubmed/35506984
http://dx.doi.org/10.1111/myc.13450
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author Atsü, Nilhan
Ergin, Çağrı
Caf, Nazlı
Türkoğlu, Zafer
Döğen, Aylin
İlkit, Macit
author_facet Atsü, Nilhan
Ergin, Çağrı
Caf, Nazlı
Türkoğlu, Zafer
Döğen, Aylin
İlkit, Macit
author_sort Atsü, Nilhan
collection PubMed
description 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 (κ = 0.90). CONCLUSION: Our results indicate that FastFung agar favours the growth of Malassezia species and should be useful in clinical mycology laboratories.
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spelling pubmed-93210002022-07-30 Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples Atsü, Nilhan Ergin, Çağrı Caf, Nazlı Türkoğlu, Zafer Döğen, Aylin İlkit, Macit Mycoses Original Articles 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 (κ = 0.90). CONCLUSION: Our results indicate that FastFung agar favours the growth of Malassezia species and should be useful in clinical mycology laboratories. John Wiley and Sons Inc. 2022-05-25 2022-07 /pmc/articles/PMC9321000/ /pubmed/35506984 http://dx.doi.org/10.1111/myc.13450 Text en © 2022 The Authors. Mycoses published by Wiley‐VCH GmbH. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Atsü, Nilhan
Ergin, Çağrı
Caf, Nazlı
Türkoğlu, Zafer
Döğen, Aylin
İlkit, Macit
Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples
title Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples
title_full Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples
title_fullStr Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples
title_full_unstemmed Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples
title_short Effectiveness of FastFung agar in the isolation of Malassezia furfur from skin samples
title_sort effectiveness of fastfung agar in the isolation of malassezia furfur from skin samples
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321000/
https://www.ncbi.nlm.nih.gov/pubmed/35506984
http://dx.doi.org/10.1111/myc.13450
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