Determination of Metalloprotease Gene in a Few Dermatophyte Species and Its Relationship with Antifungal Resistance

  • Qadisiyah Hilal Hashoosh Department of Biology, College of Science, Baghdad University, Baghdad, Iraq.
  • Alaa Mohsen.Yaseen. Al-Aaraji Department of Biology, College of Science, Baghdad University, Baghdad, Iraq.
Keywords: Quantitative PCR, Metalloprotease, Dermatophytes,, Iraq

Abstract

Introduction: Keratinophilic fungi called dermatophytes exclusively infect the stratum corneum, human hair, and nails. To infect host tissues and cause disease, dermatophytes create virulence factors
 such as keratinases and cellulase. Dermatophytes produce virulence factors such as keratinases and cellulase to infect host tissues and spread the disease.
Aim: To detect the metalloprotease gene (MEP1–5) by Real-Time Polymerase Chain Reaction analysis and its relationship with the esistance of dermatophytes against antifungals
Method: Eleven species of dermatophyte isolates obtained from Iraqi patients were diagnosed morphologically and molecularly [internal transcribed spacer (ITS) region], and were found to include the following
types: Keratinophyton indicum, Trichophyton interdigitale, Microsporum ferrugineum, Trichophyton rubrum, Trichophyton mentagrophytes, Arthroderma otae, Trichophyton simii, Microsporum canis, Trichophyton quinckeanum, Epidermophyton floccosum, and Trichophyton verrucosum. All dermatophyte species were tested for antifungal susceptibility using the disk method. The Genomic DNA extraction kit was used to extract
the genomic DNA from the fungal growth.
Results: Trichophyton simii was highly resistant to all antifungals. The percentages of genes found in the species were as follows: MEP1 and MEP2 (70%), MEP3 (81%), MEP4 (54%), and MEP5 (36%). Trichophyton simii contained all five genes MEP1–5, while Microsporum canis and Arthroderma otae contained only one gene.
Conclusion: The study showed that higher the number of genes of a dermatophyte species, higher will be its resistance to antifungals. The presence of MEP5 was found to increase the antifungal resistance. This study was considered to be the first study in Iraq to detect these genes using the qPCR method depending on the DNA extraction and the relationship with antifungal resistance.

How to cite this article:
Hashoosh QH, Al-Aaraji AMY, Determination of
Metalloprotease Gene in a Few Dermatophyte
Species and Its Relationship with Antifungal
Resistance. J Commun Dis. 2024;56(1):127-134.

DOI: https://doi.org/10.24321/0019.5138.202417

References

Chinnapun D. Virulence factors involved in pathogenicity of dermatophytes. Walailak J Sci Technol. 2015;12(7):573-80. [Google Scholar]

Achterman RR, White TC. Dermatophyte virulence factors: identifying and analyzing genes that may contribute to chronic or acute skin infections. Int J Microbiol. 2012;2012:358305. [PubMed] [Google Scholar]

Brouta F, Descamps F, Fett T, Losson B, Gerday C, Mignon B. Purification and characterization of a 43.5 kDa keratinolytic metalloprotease from Microsporum canis. Med Mycol. 2001;39(3):269-75. [PubMed] [Google Scholar]

Monod M, Lechenne B, Jousson O, Grand D, Zaugg C, Stocklin R, Grouzmann E. Aminopeptidases and

dipeptidyl-peptidases secreted by the dermatophyte Trichophyton rubrum. Microbiology (Reading). 2005;151(Pt 1):145-55. [PubMed] [Google Scholar]

Duek L, Kaufman G, Ulman Y, Berdicevsky I. The pathogenesis of dermatophyte infections in human

skin sections. J Infect. 2004;48(2):175-80. [PubMed]

[Google Scholar]

Pakshir K, Bahaedinie L, Rezaei Z, Sodaifi M, Zomorodian K. In vitro activity of six antifungal drugs against clinically important dermatophytes. Jundishapur J Microbiol. 2009;2(4):158-63. [Google Scholar]

Jain N, Sharma M, Saxena V. Identification and antifungal susceptibility testing of fungal infections in clinical samples of suspected superficial fungal infection. Indian J Dermatol Venerol Leprol. 2008;74(3):274-5.

Tamura K, Nei M, Kumar S. Prospects for inferring very large phylogenies by using the neighbor-joining method. Proc Natl Acad Sci U S A. 2004;101(30):11030- 5. [PubMed] [Google Scholar]

CLSI. Performance standards for antifungal susceptibility testing of filamentous fungi. 1st ed. CLSI Supplement

M61. Wayne, PA: Clinical and Laboratory Standards Institute; 2017.

Hashoosh QH, AL-Araji AM. Molecular identification of Tinea spp. causing tinea disease using ITS sequencing analysis. Iraqi J Biotechnol. 2023;22(1):220-8. [Google Scholar]

Fernández-Torres B, Cabañes FJ, Carrillo-Muñoz AJ, Esteban A, Inza I, Abarca L, Guarro J. Collaborative

evaluation of optimal antifungal susceptibility testing conditions for dermatophytes. J Clin Microbiol. 2002;40(11):3999-4003. [PubMed] [Google Scholar]

Datt S, Das S, Ansari MA, Sharma R, Datt T, Bhattacharya SN. Gene expression profiling of protease and non-

protease genes in Trichophyton mentagrophytes isolates from dermatophytosis patients by qRT-PCR analysis. Sci Rep. 2021;11(1):403. [PubMed] [Google Scholar]

Zhang X, Wang Y, Chi W, Shi Y, Chen S, Lin D, Jin Y. Metalloprotease genes of Trichophyton mentagrophytes are important for pathogenicity. Med Mycol. 2014;52(1):36-45. [PubMed] [Google Scholar]

Artika IM, Dewi YP, Nainggolan IM, Siregar JE,

Antonjaya U. Real-time polymerase chain reaction:

current techniques, applications, and role in COVID-19

diagnosis. Genes (Basel). 2022;13(12):2387. [PubMed]

[Google Scholar]

Mohsin MR, AL-Rubaii BA. Bacterial growth and

antibiotic sensitivity of Proteus mirabilis treated with

anti-inflammatory and painkiller drugs. Biomedicine.

;43(2):728-34.

Jalil IS, Mohammad SQ, Mohsen AK, Al-Rubaii BA.

Inhibitory activity of Mentha spicata oils on biofilms

of Proteus mirabilis isolated from burns. Biomedicine.

;43(2):748-52.

Sultan RS, Al Khayali BD, Abdulmajeed GM, Al-Rubaii BA. Exploring small nucleolar RNA host gene 3 as a

therapeutic target in breast cancer through metabolic reprogramming. Opera Med Physiol. 2023;10(4):36-47.

[Google Scholar]

Al-Jumaily RM, AL-Sheakli II, Muhammed HJ, Al-Rubaii

BA. Gene expression of Interleukin-10 and Foxp3 as

critical biomarkers in rheumatoid arthritis patients.

Biomedicine. 2023;43(4):1183-7.

Abdulrazaq RA, Mahmood WS, Alwan B, Saleh TH,

Hashim ST, Al-Rubaii BA. Biological study of protease produced by clinical isolates of Staphylococcus aureus.

Res J Pharm Technol. 2022;15(12):5415-20. [Google Scholar]

Shehab ZH, Al-Rubaii BA. Effect of D-mannose on gene expression of neuraminidase produced from different clinical isolates of Pseudomonas aeruginosa. Baghdad Sci J. 2019;16(2):291-8. [Google Scholar]

Al-Humairi RM, Al-Musawi MT, Ad’hiah AH. Bidirectional expression of toll-like receptor 7 gene in urinary bladder cancer and urinary tract infection of Iraqi patients. Gene Rep. 2019;17:100491. [Google Scholar]

Muhsin HY, Al-Humairi RM, Alshareef DQ, Ad’hiah AH. Interleukin-22 is up-regulated in serum of male patients with ankylosing spondylitis. Egypt Rheumatol. 2022 Oct 1;44(4):351-5. [Google Scholar]

Salih HS, Al-Shammari AM, Al-Rubaii BA. Intratumoral

co-administration of oncolytic Newcastle Disease

Virus and bacterial hyaluronidase enhances virus potency in tumor models. J Glob Pharma Technol. 2018;10(10):303-10. [Google Scholar]

Al-Asady IN, Mohammed MA, Saeed YS, AL-Rubaii BA. Bioenergy production from bacteria (methanogens). Bionatura. 2023;8(1):1-4. [Google Scholar]

Saleh TH, Hashim ST, Malik SN, Al-Rubaii BA. The impact some of nutrients on swarming phenomenon and detection the responsible gene RsbA in clinical isolates of Proteus mirabilis. Int J Res Pharm Sci. 2020;11(1):437-

Husain AG, Alrubaii BA. Molecular detection and expression of virulence factor encoding genes of Pseudomonas aeruginosa isolated from clinical

samples. Biomedicine. 2023;43(5):1514-9.

Rasoul LM, Marhoon AA, Albaayit SF, Ali RW, Saleh TH, Al-Rubaii BA. Cytotoxic effect of cloned EGFP gene on NCI-H727 cell line via genetically engineered gene 8. Bresam S, Al-Jumaily RM, Karim GF, Al-Rubaii BA. Polymorphism in SNP rs972283 of the KLF14 gene and genetic disposition to peptic ulcer. Biomedicine. 2023;43(1):216-20.

Ismael MK, Qaddoori YB, Shaban MN, AL-Rubaii BA. The immunohistochemical staining of vimentin and e cadherin in bladder cancer patients infected with hepatitis C virus. J Pure Appl Microbiol. 2023;17(2):1009-

[Google Scholar]

Bresam S, Alhumairi RM, Hade IM, Al-Rubaii BA. Genetic mutation rs972283 of the KLF14 gene and the incidence of gastric cancer. Biomedicine (India). 2023;43(4):1256- 60.

Al-Saadi HK, Awad HA, Saltan ZS, Hasoon BA, Abdulwahab AI, Al-Azawi KF, Al-Rubaii BA. Antioxidant and antibacterial activities of Allium sativum ethanol extract and silver nanoparticles. Trop J Nat Prod Res. 2023;7(6):3105-10. [Google Scholar]

Rasoul LM, Allami RH, Alshibib AL, Al-Rubaii BA, Sale TH. Expression and cytotoxic effect of recombinant Newcastle Disease Virus (rNDV) vector expressing enhanced green fluorescent gene in JHH5 cell line. Biomedicine. 2023;43(1):205-9.

Jawad NK, Numan AT, Ahmed AG, Saleh TH, Al-Rubaii BA. IL-38 gene expression: a new player in Graves’ ophthalmopathy patients in Iraq. Biomedicine. 2023;43(1):210-5.

Published
2024-04-25