Development of a novel polymerase chain reaction–enzyme‐linked immunosorbent assay for the diagnosis of Trichophyton rubrum onychomycosis. (5th June 2013)

• Record Type: Journal Article
• Authors: Pankewitz, F.; Nenoff, P.; Uhrlaß, S.; Bezold, G.; Winter, I.; Gräser, Y.
• Is Part Of: British journal of dermatology. Volume 168:Number 6(2013:Jun.)
• Page Start: 1236
• Page End: 1242
• Publication Date: 2013-06-05
• Subjects: Dermatology -- Periodicals; Skin -- Diseases -- Periodicals; 616.5
• DOI: 10.1111/bjd.12221
• Languages: English
• ISSNs: 0007-0963

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Summary</title> <p> <bold>Background </bold> The prevalence of onychomycosis has increased steadily in the past decade. An accurate diagnosis at the outset is important for successful and cost‐effective treatment of patients. However, current diagnostic tests for onychomycosis are not rapid, sensitive or specific.</p> <p> <bold>Objectives </bold> To develop a microsatellite‐based polymerase chain reaction (PCR)‐enzyme‐linked immunosorbent assay (MS‐ELISA) for the detection of <italic>Trichophyton rubrum</italic>, which is the most common aetiological agent of onychomycosis.</p> <p> <bold>Methods </bold> An archival set of 434 nail and skin specimens from 217 patients was included as the test sample in this study. We also compared MS‐ELISA with an earlier published topoisomerase PCR‐ELISA (TI‐ELISA) using template DNA extracted by another method.</p> <p> <bold>Results </bold> The MS‐ELISA detected the highest number of positive samples (69%) followed by direct microscopy (56%), TI‐ELISA (44%) and fungal culture (30%). When an identical DNA extraction method was applied to 120 specimens, the MS‐ELISA proved to be twice as sensitive as the TI‐ELISA.</p> <p> <bold>Conclusions </bold> We have optimized a target gene and DNA extraction method for rapid detection of <italic>T. rubrum</italic> onychomycosis.</p> </abstract>