Trapped in keratin; a comparison of dermatophyte detection in nail, skin and hair samples directly from clinical samples using culture and real-time PCR

J Microbiol Methods. 2011 Apr;85(1):62-6. doi: 10.1016/j.mimet.2011.01.023. Epub 2011 Jan 28.

Abstract

Traditionally, laboratory detection and identification of dermatophytes consists of culture and microscopy which yields results within approximately 2-6 weeks. In 2007 our medical microbiological diagnostic laboratory implemented a molecular method for the detection of dermatophytes. A real-time PCR assay was developed which simultaneously detects and identifies the most prevalent dermatophytes directly in nail, skin and hair samples and has a turnaround time of less than two days. For 1437 clinical samples, received by our diagnostic laboratory, we compared the results obtained from both culture and real-time PCR. This study showed that real-time PCR significantly increased the detection rate of dermatophytes compared to culture. Furthermore, excellent concordance between culture and real-time PCR identification was achieved.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Arthrodermataceae / isolation & purification*
  • Dermatomycoses / diagnosis*
  • Dermatomycoses / microbiology
  • Hair / microbiology*
  • Humans
  • Mycology / methods*
  • Nails / microbiology*
  • Polymerase Chain Reaction / methods*
  • Sensitivity and Specificity
  • Skin / microbiology*
  • Time Factors