Epidemiological Characterisation and Molecular Identification of Dermatophyte Infec-tions Isolated from Outpatient Clinics of The Dermatology Department at Zliten Medi-cal Center, Libya

Authors

  • Siham R. Alneebu
  • Mustafa E. Elsharif
  • Tarek M. Arshah
  • Amna H. Arltil
  • Minor J. Zeglam

DOI:

https://doi.org/10.37376/ljst.v16i1.7919

Keywords:

Dermatophytes, Fungal skin infection, Molecular Identification, PCR, Trichophyton violaceum, Zliten, Libya

Abstract

Dermatophytes are keratinophilic fungus causing superficial infections of skin, nail and hair. In recent decades, the prevalence has internationally increased, affecting about 25% of populations in different countries around the World. The aim of this study was to identify different species of dermatophytes causing dermatophytosis in patients infected with fungal skin infections using morphological, microscopic, and molecular diagnostic methods with use of Polymerase Chain Reaction (PCR) techniques. In this study a total of 100 clinical samples from skin, hair, and nails were collected from patients attending Zliten Medical Center over the period of time from 01.01.2022 until 30.5.2022.  Samples were examined microscopically using Potassium Hydroxide (KOH) 10%-20% and cultured on Sabouraud Dextrose Agar (SDA), Potato Dextrose Agar (PDA), and Dermatophyte Test Medium (DTM). Fungal isolates from positive Cultures were further investigated with PCR.  Data were analyzed using Statistical Package for the Social Sciences (SPSS) version 25. Only 22% of total samples show positivity for KOH. A 12 species were identified, with Trichophyton violaceum (25%) and Microsporum canis (20%) being the most common, followed by Trichophyton tonsurans (10%) and several less frequent species. It is worth noting, that Microsporum canis was more frequently affecting children under 11 years old und occurred more frequently in People having domestic animals. Molecular confirmation using real-time PCR (ITS1–S4 primers) showed 80% PCR positivity among culture isolates. Eight species were fully PCR-confirmed, while others showed variable detection rates. Overall, PCR has confirmed that T. violaceum and M. canis were the predominant dermatophytes in this study. The importance of this study lies in its emphasizing of the effectiveness and feasibility of using molecular identification technology for the accurate identification and early diagnosis of dermatophyte infections.

Downloads

Download data is not yet available.

Author Biographies

Siham R. Alneebu

Department of Microbiology, Faculty of Science, Alasmarya Islamic University, Zliten, Libya

Mustafa E. Elsharif

Department of Microbiology, Faculty of Science, Alasmarya Islamic University, Zliten, Libya

Tarek M. Arshah

Department of Medicine, Faculty of Medicine, Elmergeb University, Libya

Amna H. Arltil

Department of Microbiology, Laboratory of Zliten Medical Center, Libya

Minor J. Zeglam

Communicable Diseases Centre Zliten, Libya

References

Al-Aryan, A., Al-Sabah, H. Y., Al Obaid, K. A. (2022) ‘Epidemiology of dermatophytes related infections in Kuwait: a retrospective study’, Medical Mycology, 60(1), pp.76-76.

Ali-Shtayeh, M., Yaish, S., Jamous, R. M., Arda, H., & Husein, E. (2015) ‘Updating the epidemiology of dermatophyte infec-tions in Palestine with special reference to concomitant der-matophytosis’, Journal de Mycologie Médicale, 25(2), pp. 116-122.

Arshah,T.M., Al Dwibe, H and Al-Bakosh, A. (2017) ‘Tinea capitis in Patients Attending Zliten Teaching Hospital (North West of Libya)’, International Journal of Tropical Diseases & Health, 26(2), pp. 1-7

Arshah, T. M., Arshah, A. M., Alrtail, A., Elzurghany, A. (2019) ‘The Sensitivity and Role of Mycology Laboratory in Management of Superficial Fungal Infections in Zliten Teaching Hospital’, Asian Journal of Research in Dermatological Science, 2(1), pp.1-6

Altayyar I. (2012) ‘Opportunistic pathogenic fungi from the dust in Sebha Medical Centre, Libya’, Sebha Med. J; 11, pp. 87-93.

Atia, A., Ashour, A., & Elyounsi, N. (2019) ‘Trends in skin fungal infection in Tripoli, Libya, during 2007–2015’, Ibnosina Jour-nal of Medicine and Biomedical Sciences, 11(03), pp. 116-119.

Bergmans, A., Schouls, L., Van Der ENT, M., Klaassen, A., Böhm, N., & Wintermans, R. (2008) ‘Validation of PCR–reverse line blot, a method for rapid detection and identification of nine derma-tophyte species in nail, skin and hair samples’, Clinical micro-biology and infection, 14(8), pp. 778-788.

Campbell, C. K., & Johnson, E. M. (2013) Identification of pathogen-ic fungi: John Wiley & Sons. 31-79.

Dismukes, W. E., Pappas, P. G., Sobel, J. D. (2003) Clinical mycolo-gy. Oxford University Press, 7-15,370-384

Ellabib, M., Khalifa, Z., & Kavanagh, K. (2002) ‘Dermatophytes and other fungi associated with skin mycoses in Tripoli, Libya’, Mycoses, 45(3‐4), pp. 101-104.

Galliano, I., Dapra, V., Zaniol, E., Alliaudi, C., Graziano, E., Mon-tanari, P., Bergallo, M. (2021) ‘Comparison of methods for iso-lating fungal DNA’, Practical Laboratory Medicine, 25, 1-5.

Gohar, N., El-Batal, H., Elawady, B., & Samir, N. (2019) ‘Phenotypic methods versus PCR-RFLP for the identification of dermato-phyte species isolated from patients with dermatophytosis in Egypt’, African Journal of Clinical and Experimental Microbiolo-gy, 20(2), pp. 117-126.

Havlickova, B., Czaika, V., Friedric, M. (2008) ‘Epidemiological trends in skin mycoses worldwide’, Mycoses, 51(4), pp. 2-15.

Khan, S., Shamsuzzaman, S., Rahman, A., Ashekin, N., Mahmud, R., Sharmin, R., Haque, F. (2021) ‘Isolation and Identification of Dermatophytes Causing Dermatophytosis at a Tertiary Care Hospital in Bangladesh’, Archives of Clinical and Biomedical Re-search, 5(3), pp. 437-451.

Kidd, S., Halliday, C., Alexiou, H., & Ellis, D. (2016) Descriptions of medical fungi (Vol. 3). David Ellis.195-218.

Kromer, C., Celis, D., Hipler, U. C., Zampeli, V. A., Mößner, R., & Lippert, U. (2021) ‘Dermatophyte infections in children com-pared to adults in Germany: a retrospective multicenter study in Germany. JDDG’, Journal Der Deutschen Dermatologischen Gesellschaft, 19(7), pp. 993-1001.

Li, H. C., Bouchara, J.-P., Hsu, M. M.-L., Barton, R., Su, S., & Chang, T. C. (2008) ‘Identification of dermatophytes by sequence analysis of the rRNA gene internal transcribed spacer regions’, Journal of medical microbiology, 57(5), pp. 592-600.

Magagnin, C. M., Stopiglia, C. D. O., Vieira, F. J., Heidrich, D., Ma-chado, M., Vetoratto, G., Scroferneker, M. L. (2011) ‘Antifungal susceptibility of dermatophytes isolated from patients with chronic renal failure’, Anais brasileiros de dermatologia, 86, pp. 694-701.

Marcos-Tejedor, F., Mota, M., Iglesias-Sánchez, M. J., Mayordomo, R., & Gonçalves, T. (2021) ‘Identification of fungi involved in onychomycosis in patients of a Spanish rural area’, Journal of Fungi, 7(8), pp. 623.1-8.

Mohammadi, R., Abastabar, M., Mirhendi, H., Badali, H., Shadzi, S., Chadeganipour, M., Haghani, I. (2015) ‘Use of restriction fragment length polymorphism to rapidly identify dermato-phyte species related to dermatophytosis’, Jundishapur journal of microbiology, 8(6), pp. 1-6.

Ndiaye, M., Sacheli, R., Diongue, K., Adjetey, C., Darfouf, R., Seck, M. C., Hayette, M.-P. (2021) ‘Evaluation of the multiplex real-time PCR DermaGenius® assay for the detection of dermato-phytes in hair samples from Senegal’, Journal of Fungi, 8(1), pp. 11.1-13.

Santhosh, P., George, M and Nandakumar, G. (2024) ‘Demonstra-tion of fungi in superficial mycosis: Skin scraping and potassi-um hydroxide mount’, Journal of Skin and Sexually Transmitted Diseases, 6(1), pp. 77-79

Sciortino J.r., C. V. (2017) Atlas of clinically important fungi: John Wiley & Sons. 135-166.

Sjahril, R., Hamid, F., Yulianingsih, A., Prastiwi, N., Awaluddin, A., Nuryanti, S., Bahar, B. (2017) ‘Identification of Dermatophytes by Multiplex-Polymerase Chain Reaction, Polymerase Chain Reaction-Restriction Fragment Length Polymorphism ITS1-ITS4 Primers and MvaI, and Polymerase Chain Reaction (GACA) 4 Primer’, UNEJ e-Proceeding, pp. 132-135.

Walsh, T. J., Hayden, R. T., & Larone, D. H. (2018) Larone's medi-cally important fungi: A guide to identification: John Wiley & Sons. 257-282.

Wisselink, G., Van Zanten, E., & Kooistra-Smid, A. (2011) ‘Trapped in keratin; a comparison of dermatophyte detection in nail, skin and hair samples directly from clinical samples using cul-ture and real-time PCR’, Journal of microbiological methods, 85(1), pp. 62-66.

Downloads

Published

2026-08-10

How to Cite

Siham R. Alneebu, Mustafa E. Elsharif, Tarek M. Arshah, Amna H. Arltil, & Minor J. Zeglam. (2026). Epidemiological Characterisation and Molecular Identification of Dermatophyte Infec-tions Isolated from Outpatient Clinics of The Dermatology Department at Zliten Medi-cal Center, Libya. Libyan Journal of Science &Amp;Technology, 16(1), 322–327. https://doi.org/10.37376/ljst.v16i1.7919

Issue

Section

Articles