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Antifungal susceptibility and in vitro virulence characteristics of clinical Magnusiomyces/Saprochaete isolates: a multicenter study from Türkiye
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  • Published: 15 March 2026

Antifungal susceptibility and in vitro virulence characteristics of clinical Magnusiomyces/Saprochaete isolates: a multicenter study from Türkiye

  • Ali Ozturk1 na1,
  • Merve Aydin2 na1,
  • Elif Ayca Sahin3,
  • Dolunay Gulmez4,
  • Elif Seren Tanrıverdi5,
  • Baris Otlu5,
  • Sevtap Arikan-Akdagli4,
  • Bashar Ibrahim6,
  • Betil Ozhak7,8,
  • Ozlem Koyuncu Ozyurt8,
  • Yasemin Oz9,
  • Sebahat Aksaray10,
  • Deniz Turan10,
  • Muge Aslan11,
  • Ayse Baris12,
  • Ayse Nedret Koc13,
  • Gonca Erkose Genc14,
  • Zayre Erturan14,
  • Beyza Ener15,
  • Nazmiye Ulku Tuzemen15,
  • Ebru Evren16,
  • Zeynep Ceren Karahan16,
  • Aydin Karaarslan16,
  • Melda Ozdamar17,
  • Berna Gultekin Korkmazgil18,
  • Halil Er19,
  • Ozgul Cetinkaya19,
  • Zeynep Arzu Ilki20,
  • Elvan Sayin20,
  • Asuman Birinci21,
  • Esra Ozkaya22,
  • Ilknur Tosun22,
  • Rabiye Altinbas23,
  • Emine Kucukates24 &
  • …
  • Ayse Kalkanci3 

Scientific Reports , Article number:  (2026) Cite this article

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Subjects

  • Diseases
  • Microbiology

Abstract

Invasive infections due to Magnusiomyces/Saprochaete species are an emerging problem in immunocompromised patients and are often underrecognized because of misidentification and intrinsic resistance to some antifungals. This multicenter study investigated the species distribution, antifungal susceptibility patterns, and key virulence traits of clinical isolates from Türkiye. A total of 133 clinical isolates collected between 2010 and 2024 from 18 hospitals in 10 cities were identified by MALDI-TOF MS and ITS/LSU sequencing. MICs of amphotericin B, fluconazole, voriconazole, itraconazole, posaconazole, and flucytosine were determined using the EUCAST broth microdilution method. Biofilm formation and esterase, caseinase, secreted aspartyl proteinase, phospholipase, and hemolysin activities were assessed phenotypically. Sequencing identified 107 isolates (80.4%) as Magnusiomyces capitatus and 26 (19.6%) as Magnusiomyces clavatus, MALDI-TOF MS identified 106 (79.7%) as M. capitatus and 27 isolates (20.3%) as M. clavatus. There was 99.2% agreement between MALDI-TOF MS and sequencing results. Voriconazole, amphotericin B, and posaconazole showed the lowest MICs, whereas fluconazole displayed wide MIC ranges and limited activity. Overall, 97.7% of isolates were strong biofilm producers, with significantly higher biofilm production in M. capitatus. In contrast, M. clavatus showed higher caseinase and esterase activity. This study provides the most extensive multicenter dataset on Magnusiomyces/Saprochaete in Türkiye and underscores their considerable pathogenic potential through strong biofilm formation and tissue-degrading enzyme activities. Accurate species-level identification using MALDI-TOF MS supported by molecular methods is essential, and limited fluconazole activity suggests that voriconazole and amphotericin B should be prioritized in species-guided treatment strategies.

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Data availability

The DNA sequence datasets generated in this study and supporting the findings are openly available in NCBI GenBank at “https://www.ncbi.nlm.nih.gov/nuccore/?term=PV273725:PV273820[accn]” under accession numbers PV273725–PV273820.

Abbreviations

AMB:

Amphotericin B

BAL:

Bronchoalveolar Lavage

CFU:

Colony forming unit

CSF:

Cerebrospinal fluid

DMSO:

Dimethyl sulfoxide

DNA:

Deoxyribonucleic acid

EUCAST:

European Committee on Antimicrobial Susceptibility Testing

FLU:

Fluconazole

ICU:

Intensive care unit

IFIs:

Invasive fungal infections

ITS:

Internal transcribed spacer

ITR:

Itraconazole

LSU:

Large subunit (ribosomal DNA)

MALDI-TOF MS:

Matrix-assisted laser desorption ionisation-time-of-flight mass spectrometry

MIC:

Minimum inhibitory concentration

ML:

Maximum likelihood

MTT:

3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (assay)

OD:

Optical density

PBS:

Phosphate-buffered saline

PCR:

Polymerase chain reaction

POS:

Posaconazole

RPMI:

Roswell Park Memorial Institute (medium)

SAP:

Secreted aspartyl proteinase

SDA:

Sabouraud dextrose agar

VOR:

Voriconazole

5-FC:

5-Flucytosine

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Acknowledgements

“This work is respectfully dedicated, with deep gratitude, to the memory of our esteemed mentor Prof. Dr. Emel TÜMBAY, whom we lost in 2025, in recognition of her enduring and visionary contributions to the field of medical mycology.”

Funding

This study was supported by the Scientific Research Projects Coordination Unit of Nigde Omer Halisdemir University within the scope of project no. SAT 2024/9-BAGEP.

Author information

Author notes
  1. Ali Ozturk and Merve Aydin contributed equally to this work.

Authors and Affiliations

  1. Department of Medical Microbiology, Faculty of Medicine, Nigde Omer Halisdemir University, Nigde, Turkey

    Ali Ozturk

  2. Department of Medical Microbiology, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey

    Merve Aydin

  3. Department of Medical Microbiology, Faculty of Medicine, Gazi University, Ankara, Turkey

    Elif Ayca Sahin & Ayse Kalkanci

  4. Department of Medical Microbiology, Faculty of Medicine, Hacettepe University, Ankara, Turkey

    Dolunay Gulmez & Sevtap Arikan-Akdagli

  5. Department of Medical Microbiology, Faculty of Medicine, Inonu University, Malatya, Turkey

    Elif Seren Tanrıverdi & Baris Otlu

  6. Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Suleyman Demirel University, Isparta, Turkey

    Bashar Ibrahim

  7. Department of Medical Microbiology, Faculty of Medicine, İzmir Bakırçay University, İzmir, Turkey

    Betil Ozhak

  8. Department of Medical Microbiology, Faculty of Medicine, Akdeniz University, Antalya, Turkey

    Betil Ozhak & Ozlem Koyuncu Ozyurt

  9. Department of Medical Microbiology, Faculty of Medicine, Eskişehir Osmangazi University, Eskisehir, Turkey

    Yasemin Oz

  10. Department of Medical Microbiology, Haydarpaşa Numune Training and Research Hospital, Health Sciences University, Istanbul, Turkey

    Sebahat Aksaray & Deniz Turan

  11. Department of Medical Microbiology, Etlik City Hospital, Ankara, Turkey

    Muge Aslan

  12. Department of Medical Microbiology and Medical Mycology, Sisli Hamidiye Etfal Training and Research Hospital, Health Sciences University, Istanbul, Turkey

    Ayse Baris

  13. Department of Medical Microbiology, Faculty of Medicine, Erciyes University, Kayseri, Turkey

    Ayse Nedret Koc

  14. Department of Medical Microbiology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey

    Gonca Erkose Genc & Zayre Erturan

  15. Department of Medical Microbiology, Faculty of Medicine, Bursa Uludag University, Bursa, Turkey

    Beyza Ener & Nazmiye Ulku Tuzemen

  16. Department of Medical Microbiology, Faculty of Medicine, Ankara University, Ankara, Turkey

    Ebru Evren, Zeynep Ceren Karahan & Aydin Karaarslan

  17. Department of Clinical Microbiology, Anadolu Medical Center, Izmit, Turkey

    Melda Ozdamar

  18. Department of Medical Microbiology, Faculty of Medicine, Aydin Adnan Menderes University, Aydin, Turkey

    Berna Gultekin Korkmazgil

  19. Department of Medical Microbiology, Antalya Training and Research Hospital, Antalya, Turkey

    Halil Er & Ozgul Cetinkaya

  20. Department of Medical Microbiology, Faculty of Medicine, Marmara University, Istanbul, Turkey

    Zeynep Arzu Ilki & Elvan Sayin

  21. Department of Medical Microbiology, Faculty of Medicine, Ondokuz Mayıs University, Samsun, Turkey

    Asuman Birinci

  22. Department of Medical Microbiology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey

    Esra Ozkaya & Ilknur Tosun

  23. Department of Medical Microbiology, Izmir City Hospital, Izmir, Turkey

    Rabiye Altinbas

  24. Department of Medical Microbiology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey

    Emine Kucukates

Authors
  1. Ali Ozturk
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  2. Merve Aydin
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  28. Zeynep Arzu Ilki
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  32. Ilknur Tosun
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  33. Rabiye Altinbas
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Contributions

A.O: Conceptualization; Methodology; Formal analysis; Investigation; Data curation; Writing-original draft; Writing-review&editing; M.A: Investigation; Data curation; Writing-original draft; Writing-review&editing; E.A.S.; D.G.; E.S.T.; B.O.; Methodology; Investigation; S.A.A: Conceptualization; Methodology; Investigation; Data curation; Writing-original draft; Writing-review&editing; Supervision, B.I: Data curation; Writing-original draft; B.O.; O.K.O.; Y.O.; S.A.; D.T.; M.A.; A.B.; A.N.K.; G.E.G; Z.E; B.E.; N.U.T.; E.E.; Z.C.K.; A.K.; M.O.; B.G.K.; H.E.; O.C.; Z.A.I.; E.S.; A.B.; E.O.; I. T.; R. A.; E. K.; provided clinical isolates; A.K: Conceptualization; Methodology; Investigation; Data curation; Writing-original draft; Writing-review&editing; Supervision. All authors read and approved the final version of the manuscript.

Corresponding author

Correspondence to Ali Ozturk.

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Competing interests

The authors declare no competing interests.

Ethical approval

This study protocol was approved by the Ethics Committee of Nigde Omer Halisdemir University, Nigde, Türkiye (Approval No: 2022/92, Date: 14.09.2022).

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Ozturk, A., Aydin, M., Sahin, E.A. et al. Antifungal susceptibility and in vitro virulence characteristics of clinical Magnusiomyces/Saprochaete isolates: a multicenter study from Türkiye. Sci Rep (2026). https://doi.org/10.1038/s41598-026-42967-1

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  • Received: 25 December 2025

  • Accepted: 28 February 2026

  • Published: 15 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-42967-1

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Keywords

  • Magnusiomyces capitatus
  • Magnusiomyces clavatus
  • Saprochaete
  • Antifungal susceptibility
  • Virulence factors
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