# Diversity and Antifungal Susceptibility of Malassezia spp. Isolated From Brazilian Patients With Pityriasis Versicolor and Seborrheic Dermatitis

**Authors:** Diogo Coelho de Pádua Oliveira, Ana Paula Possa, Ana Raquel de Oliveira Santos, Ana Kleiber P. Borges, Patrícia Silva Cisalpino, Raquel Vilela, Carlos Augusto Rosa, Susana Johann

PMC · DOI: 10.1111/myc.70171 · 2026-03-27

## TL;DR

This study analyzed Malassezia species in Brazilian patients with skin conditions and found varying antifungal resistance levels.

## Contribution

The study reports the first identification of rare Malassezia species in Brazil and their antifungal susceptibility profiles.

## Key findings

- M. furfur was the most common species among Brazilian patients with PV and SD.
- All isolates showed high resistance to caspofungin and isoconazole.
- Itraconazole and ketoconazole were the most effective antifungals tested.

## Abstract

Malassezia spp. are part of the microbiota of many animals, including humans. However, under certain conditions, they can become pathogenic. Diseases associated with Malassezia include pityriasis versicolor (PV), seborrheic dermatitis (SD), Malassezia folliculitis, atopic dermatitis, psoriasis and fungemia.

The present study aimed to describe the distribution of Malassezia species among Brazilian patients with PV and SD and to evaluate their susceptibility profiles to common antifungals.

In this study, 102 clinical samples from patients with PV or SD were analysed. Clinical isolates of Malassezia were identified at the species level by sequencing the D1/D2 variable domains of the large subunit rRNA gene. Antifungal susceptibility was assessed using a modified microbroth dilution method adapted for the growth of Malassezia species.

Among the 40 cultures obtained, six Malassezia species were identified. M. furfur was the most prevalent species (40.0%), followed by M. sympodialis (27.5%), 
M. globosa
 (15.0%), 
M. japonica
 (7.5%) and both M. yamatoensis and M. slooffiae (5.0% each). All isolates exhibited high MICs to caspofungin (> s16 μg/mL) and to isoconazole (MIC₅₀ = 8 μg/mL). Miconazole and clotrimazole showed MIC₅₀ values of 4 μg/mL, while itraconazole and ketoconazole were more active, with an MIC₅₀ of 0.125 μg/mL.

This study showed the diversity of Malassezia species causing PV and SD in Brazil, including the rare species M. yamatoensis and 
M. japonica
. These findings highlight the importance of antifungal susceptibility testing for these species to guide appropriate therapy.

## Linked entities

- **Chemicals:** caspofungin (PubChem CID 16119814), isoconazole (PubChem CID 3760), miconazole (PubChem CID 4189), clotrimazole (PubChem CID 2812), itraconazole (PubChem CID 55283), ketoconazole (PubChem CID 3823)
- **Diseases:** pityriasis versicolor (MONDO:0005915), seborrheic dermatitis (MONDO:0006608)
- **Species:** Malassezia furfur (taxon 55194), Malassezia sympodialis (taxon 76777), Malassezia globosa (taxon 76773), Malassezia japonica (taxon 223818), Malassezia yamatoensis (taxon 253288), Malassezia slooffiae (taxon 76776)

## Full-text entities

- **Genes:** CARD9 (caspase recruitment domain family member 9) [NCBI Gene 64170] {aka CANDF2, IMD103, hCARD9}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, MBL2 (mannose binding lectin 2) [NCBI Gene 4153] {aka COLEC1, HSMBPC, MBL, MBL2D, MBP, MBP-C}, SPHK1 (sphingosine kinase 1) [NCBI Gene 8877] {aka SPHK}
- **Diseases:** Malassezia folliculitis (MESH:D005499), Diseases (MESH:D004194), fungal (MESH:D009181), fungemia (MESH:D016469), pancreatic ductal adenocarcinoma (MESH:D021441), inflammatory skin (MESH:D012878), inflammatory bowel disease (MESH:D015212), Pancreatic ductal adenocarcinoma (PDA) tumours (MESH:D010190), SD (MESH:D012628), psoriasis (MESH:D011565), associated (MESH:D018886), cancer (MESH:D009369), Crohn's disease (MESH:D003424), atopic dermatitis (MESH:D003876), skin diseases (MESH:D012871), inflammatory (MESH:D007249), Malassezia (MESH:D014010), colitis (MESH:D003092), breast cancer (MESH:D001943)
- **Chemicals:** chloroform (MESH:D002725), ethanol (MESH:D000431), CLO (MESH:D006997), Cetoconazole (-), Ni (MESH:D009532), isoamyl alcohol (MESH:C029683), Clotrimazole (MESH:D003022), posaconazole (MESH:C101425), lipid (MESH:D008055), CASP (MESH:D003565), Caspofungin (MESH:D000077336), Itraconazole (MESH:D017964), EDTA (MESH:D004492), SDS (MESH:D012967), ketoconazole (MESH:D007654), phenol (MESH:D019800), Cremophor (MESH:C022131), dimethyl sulfoxide (MESH:D004121), NaCl (MESH:D012965), water (MESH:D014867), Miconazole (MESH:D008825), isopropyl alcohol (MESH:D019840), CET (MESH:D002512), Tween 80 (MESH:D011136), KOH (MESH:C029943), Isoconazole (MESH:C020382), fluconazole (MESH:D015725), sodium acetate (MESH:D019346), HCl (MESH:D006851), Tween 40 (MESH:C068430)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Malassezia slooffiae (species) [taxon 76776], Shewanella sp. P28 (species) [taxon 1405511], Homo sapiens (human, species) [taxon 9606], Malassezia arunalokei (species) [taxon 1514897], Malassezia restricta (species) [taxon 76775], Malassezia psittaci (species) [taxon 1821823], Malassezia pachydermatis (species) [taxon 77020], Malassezia globosa (species) [taxon 76773], Malassezia dermatis (species) [taxon 169489], M. gallinae [taxon 69892], Malassezia furfur (Pityriasis (Tinea) versicolor infection agent, species) [taxon 55194], Malassezia sympodialis (species) [taxon 76777], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

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Source: https://tomesphere.com/paper/PMC13032048