# Clinical and Mycological Profiles of Chronic and Recalcitrant Dermatophytosis: Türkiye, 2022–2024

**Authors:** Murat Durdu, Hazal Kandemir, Ayşe Sultan Karakoyun, Pavlína Lysková, Daniela Kolarczyková, Oğuzhan Bingöl, Yasemin Erdem, Funda Aktürk-Gözel, Özlem Su-Küçük, Melisa Özay, Aslan Yürekli, İlayda Muslu, İsa An, Sinan Özçelik, Tuğba Falay-Gür, Tuğba Tehçi, Abdullah Demirbaş, Gözde Ulutaş-Demirbaş, Tuğba Atak, Kaan Taşolar, Büşra Acar-Mantar, Mehmet Kamil Mülayim, Rebiay Kıran, Ayşe Tülin Mansur, İrem Yanatma, Sertaç Sever, Yeşim Yayla-Öztürk, Selami Aykut Temiz, Rabia Öztaş-Kara, Fatma Uzun, Ferit Kuşçu, Gonca Erköse-Genç, Zayre Erturan, Sybren de Hoog, Vit Hubka, Macit Ilkit

PMC · DOI: 10.1007/s11046-026-01058-5 · Mycopathologia · 2026-02-18

## TL;DR

This study analyzed 91 patients in Türkiye with chronic fungal infections and found high resistance to antifungal drugs in certain fungi, suggesting new treatment approaches.

## Contribution

The study identifies specific genetic mutations in fungi and evaluates novel adjunct therapies for drug-resistant dermatophytosis.

## Key findings

- Most isolates were Trichophyton mentagrophytes ITS genotype VIII with high resistance to terbinafine and fluconazole.
- Phe397Leu and Tyr414His substitutions were common in TmVIII isolates, with five novel substitutions observed.
- Adjunct therapies with resveratrol and curcumin showed promise in treating resistant infections despite in vitro limitations.

## Abstract

This study investigated the treatment outcomes of 91 patients with chronic and recalcitrant dermatophytosis from 20 hospitals in Türkiye between June 2022 and March 2024, as well as the in vitro antifungal susceptibility and squalene epoxidase (SQLE) substitution profiles of the dermatophytes obtained from these patients. Molecular identification by sequencing 91 isolates, revealed 76 Trichophyton mentagrophytes ITS genotype VIII (TmVIII; also known as T. indotineae) isolates, 13 Trichophyton rubrum, one Trichophyton tonsurans, and one Microsporum canis. The Phe397Leu substitution predominated in the SQLE, and Tyr414His co-occurred in nine TmVIII isolates. Five novel substitutions were observed in TmVIII. Among 13 T. rubrum isolates, three showed different SQLE substitution patterns compared to the wild-type strain. EUCAST antifungal susceptibility testing revealed high minimum inhibitory concentrations (MICs) for terbinafine (TRB) (> 0.25 mg/L) and for fluconazole (FLZ) (≥ 16 mg/L), indicating resistance in most TmVIII isolates. Of the 91 patients, 83 responded to FLZ, itraconazole (ITZ), TRB, or voriconazole-based regimens. While adjunct therapy with FLZ and resveratrol (RES) led to improvement in 28/29 patients despite their high in vitro inhibition concentrations, ITZ and curcumin (CUR) therapy was successful in 3/3 patients. However, the in vitro efficiency of CUR could not be evaluated. These findings highlight the local occurrence of specific SQLE substitutions, underscore the importance of EUCAST MIC testing combined with SQLE sequencing for surveillance, and support further evaluation of RES and CUR as an adjunct in TRB-resistant TmVIII.

The online version contains supplementary material available at 10.1007/s11046-026-01058-5.

## Linked entities

- **Genes:** SQLE (squalene epoxidase) [NCBI Gene 6713]
- **Chemicals:** terbinafine (PubChem CID 1549008), fluconazole (PubChem CID 3365), itraconazole (PubChem CID 55283), voriconazole (PubChem CID 71616), resveratrol (PubChem CID 5056), curcumin (PubChem CID 969516)
- **Diseases:** dermatophytosis (MONDO:0004678)
- **Species:** Trichophyton mentagrophytes (taxon 523103), Trichophyton rubrum (taxon 5551), Trichophyton tonsurans (taxon 34387), Microsporum canis (taxon 63405)

## Full-text entities

- **Genes:** TRB (T cell receptor beta locus) [NCBI Gene 6957] {aka TCRB, TRB@}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, SQLE (squalene epoxidase) [NCBI Gene 6713]
- **Diseases:** tinea faciei (MESH:C000656845), diabetes (MESH:D003920), dyshidrotic eczema (MESH:D011146), post (MESH:D000094025), Dermatophytide (MESH:C000656844), T. indotineae infection (MESH:D007239), maculopapular eruption (MESH:D003875), asthma (MESH:D001249), onychomycosis (MESH:D014009), epilepsy (MESH:D004827), Recalcitrant Dermatophytosis (MESH:D014005), inflammatory (MESH:D007249), DK-Trub-sqle-WT (MESH:C565618), hyperpigmentation (MESH:D017495), hypertension (MESH:D006973), erythema (MESH:D004890), dermatophyte infection (MESH:D003881), OM313296.1 (MESH:C538557), HIV (MESH:D015658), tinea cruris (MESH:D000084002), Seizures (MESH:D012640), fungal (MESH:D009181), itching (MESH:D011537), sickle cell anemia (MESH:D000755)
- **Chemicals:** azole (MESH:D001393), KCZ (MESH:D007654), CUR (MESH:D003474), C1386 (-), TRB (MESH:D000077291), nylon (MESH:D009757), gentamicin (MESH:D005839), cycloheximide (MESH:D003513), sertaconazole (MESH:C061131), RES (MESH:D000077185), Tween 20 (MESH:D011136), VRZ (MESH:D065819), DMSO (MESH:D004121), chloramphenicol (MESH:D002701), phenobarbital (MESH:D010634), ITZ (MESH:D017964), luliconazole (MESH:C112528), triazole (MESH:D014230), water (MESH:D014867), FLZ (MESH:D015725), agarose (MESH:D012685), PCZ (MESH:C101425)
- **Species:** Trichophyton tonsurans (species) [taxon 34387], Trichophyton equinum (species) [taxon 63418], Homo sapiens (human, species) [taxon 9606], Arthrodermataceae (dermatophytes, family) [taxon 34384], Trichophyton mentagrophytes (species) [taxon 523103], Paracoccidioides brasiliensis (species) [taxon 121759], Lodderomyces parapsilosis (species) [taxon 5480], Pichia kudriavzevii (species) [taxon 4909], Aspergillus flavus (species) [taxon 5059], Arachis hypogaea (goober, species) [taxon 3818], Trichophyton indotineae (species) [taxon 2739387], A. flavus [taxon 315677], Curcuma longa (turmeric, species) [taxon 136217], Microsporum canis (species) [taxon 63405], Trichophyton rubrum (species) [taxon 5551], Cryptococcus neoformans (Cryptococcus neoformans serotype A, species) [taxon 5207], Trichophyton benhamiae (species) [taxon 63400]
- **Mutations:** Ala448Thr, Pro423Ser, Phe446Leu, Ala445Gly, L in 71, Tyr414His, Phe378Leu, Phe446Val, Tyr414His, Thr414His, Phe397Leu, Phe446Gly, Val436Gly, Phe446Cys, Phe397Leu, Leu393Ser, L for T

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916938/full.md

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Source: https://tomesphere.com/paper/PMC12916938