Title of article :
Real-time PCR: A rapid and sensitive method for diagnosis of dermatophyte induced onychomycosis, a comparative study
Author/Authors :
Emam, Sherin M Medical Microbiology & Immunology - Faculty of Medicine - Benha University, Benha, Egypt , Abd El-salam, Osama H Dermatology & Andrology Departments - Faculty of Medicine - Benha University, Benha, Egypt
Pages :
8
From page :
83
To page :
90
Abstract :
Onychomycosis is the most common nail disorder, accounting for up to 50% of all nailproblems and about 30% of cutaneous fungal infections. Treatment of onychomycosis is expensive.It requires long-term therapy with an oral antifungal medication with potential side effects.Therefore, a proper diagnosis of infection is needed. Aim of the study: This study aimed to comparereal time PCR using novel primers targeting the pan-dermatophyte-specific sequence of the chitinsynthase 1 gene (CHS1) with nested PCR targeting the same gene, KOH microscopy, direct microscopyin relation to culture for diagnosis of clinically suspected onychomycosis.Subjects and methods: This study was conducted during the period from April 2013 through May2014. Eighty patients attending Outpatient Dermatology and Andrology clinic at Benha UniversityHospital were included in this study. They were 30 females and 50 males with suspected clinicaldiagnosis of onychomycosis. Their ages ranged from 22 to 77 years. Thirty eight of them were livingin rural areas, while the other 42 came from urban areas. Nail scrapings were collected andexamined by the following: direct KOH microscopic examination, culture, nested PCR using doublesets of primers and finally real time PCR. Results: As regards direct microscopy by KOHexamination, 66 (82.50%) cases were positive, while 14 (17.5%) were negative. Culture was positiveonly in 38 (47.5%) of nail samples revealing different fungi. Dermatophytes were isolated from 30(37.5%) cases; most of them were Trichophyton mentagrophytes, and in 8 cases the only isolated non-dermatophytic organism was Aspergillus Niger spp. (10.00%). Nested PCR was positive in 52(65.00%) of nail samples while real time PCR was positive in 58 (72.5%) of nail samples.Conclusion: Real-time PCR followed by melting-point analysis, gives a diagnostic tool that has ahigher sensitivity (93.3%) and is faster than nested PCR (73.3%) and other conventional methods.
Keywords :
Onychomycosis , Dermatophytes , Nested PCR , Real time PCR
Journal title :
Alexandria Journal of Medicine(AJM)
Serial Year :
2016
Journal title :
Alexandria Journal of Medicine(AJM)
Record number :
2682900
Link To Document :
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