Literature DB >> 18487596

Diagnosis of Trichophyton rubrum from onychomycotic nail samples using polymerase chain reaction and calcofluor white microscopy.

Aditya K Gupta1, Muhammad Zaman, Jagpal Singh.   

Abstract

BACKGROUND: A high rate of false-negative dermatophyte detection is observed when the most common laboratory methods are used. These methods include microscopic observation of potassium hydroxide-digested nail clippings and culture methods using agar-based media supplemented with cycloheximide, chloramphenicol, and gentamicin to isolate dermatophytes. Microscopic detection methods that use calcofluor white staining or periodic acid-Schiff staining may also be substituted for and have previously been reported to be more sensitive than potassium hydroxide-digested nail clippings.
METHODS: Trichophyton rubrum infections were detected directly from nails in a double-round polymerase chain reaction assay that uses actin gene-based primers. This method was compared with detection of fungal hyphae by using calcofluor white fluorescence microscopy of nail samples collected from 83 patients with onychomycosis who were undergoing antifungal drug therapy.
RESULTS: Twenty-six of 83 samples (31.3%) were found to be positive by calcofluor white fluorescence microscopy, and 21 of 83 samples (25.3%) yielded positive results for T rubrum when actin gene-based primers in a double-round polymerase chain reaction assay were used. When calcofluor white fluorescence microscopy and polymerase chain reaction assay were used, the combined detection was 46.9% compared with 31.3% when calcofluor microscopy and culture of nail samples on Sabouraud's dextrose agar supplemented with cycloheximide, chloramphenicol, and gentamicin were used.
CONCLUSIONS: These results suggest that the use of a direct DNA protocol is an alternative method for detecting Trichophyton infections. When this protocol is used, the presence of T rubrum DNA is directly detected. However, the viability of the dermatophyte is not addressed, and further methods need to be developed for the detection of viable T rubrum directly from nail samples.

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Year:  2008        PMID: 18487596     DOI: 10.7547/0980224

Source DB:  PubMed          Journal:  J Am Podiatr Med Assoc        ISSN: 1930-8264


  5 in total

1.  Onychomycosis in qassim region of saudi arabia: a clinicoaetiologic correlation.

Authors:  Muhammad Shahzad; Abdullateef A Alzolibani; Ahmad A Al Robaee; Ghada A Bin Saif; Ibrahim H K Babikir; Eltuhami M Abdel-Magied; Abeer E Elsayed
Journal:  J Clin Diagn Res       Date:  2014-08-20

2.  Rapid detection of dermatophytes and Candida albicans in onychomycosis specimens by an oligonucleotide array.

Authors:  Huan Wen Han; Mark Ming-Long Hsu; Jong Soo Choi; Chao-Kai Hsu; Hsin Yi Hsieh; Hsin Chieh Li; Hsien Chang Chang; Tsung Chain Chang
Journal:  BMC Infect Dis       Date:  2014-11-07       Impact factor: 3.090

3.  Comparison of fungal fluorescent staining and ITS rDNA PCR-based sequencing with conventional methods for the diagnosis of onychomycosis.

Authors:  F Bao; Y Fan; L Sun; Y Yu; Z Wang; Q Pan; C Yu; H Liu; F Zhang
Journal:  J Eur Acad Dermatol Venereol       Date:  2018-02-27       Impact factor: 6.166

4.  Evaluation Of The Efficacy Of Fluorescent Staining And Chicago Sky Blue Staining As Methods For Diagnosis Of Dermatophytosis In Hair And Nails.

Authors:  Basma Mourad; Mayada Ismail; Soha Hawwam; Mina Msseha; Reham Hassan
Journal:  Clin Cosmet Investig Dermatol       Date:  2019-10-09

5.  Photodynamic action of protoporphyrin IX derivatives on Trichophyton rubrum.

Authors:  Rogério Rodrigo Ramos; Dora Inês Kozusny-Andreani; Adjaci Uchôa Fernandes; Mauricio da Silva Baptista
Journal:  An Bras Dermatol       Date:  2016-04       Impact factor: 1.896

  5 in total

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