Validation of PCR–reverse line blot, a method for rapid detection and identification of nine dermatophyte species in nail, skin and hair samples A.M.C.

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Presentation transcript:

Validation of PCR–reverse line blot, a method for rapid detection and identification of nine dermatophyte species in nail, skin and hair samples A.M.C. Bergmans, L.M. Schouls, M. van der Ent, A. Klaassen, N. Böhm, R.G.F. Wintermans Clinical Microbiology and Infection Volume 14, Issue 8, Pages 778-788 (August 2008) DOI: 10.1111/j.1469-0691.2008.02036.x Copyright © 2008 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 1 Typical result of reverse line blot hybridization of dermatophyte PCR products from clinical samples and from isolates. Horizontal lanes: genus-specific and species-specific oligonucleotide probes (three lanes per probe). Vertical lanes: PCR products from clinical samples (lanes 1–30) and from dermatophyte isolates (lanes 32–39). Clinical Microbiology and Infection 2008 14, 778-788DOI: (10.1111/j.1469-0691.2008.02036.x) Copyright © 2008 European Society of Clinical Infectious Diseases Terms and Conditions