2019
DOI: 10.1111/bjd.17512
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Development and evaluation of a pan‐dermatophyte polymerase chain reaction with species‐level identification using sloppy molecular beacon probes

Abstract: Summary Background Conventional laboratory diagnosis of dermatophyte infection is cumbersome and time‐consuming. Objectives We aimed to establish a simple, robust and rapid molecular diagnostic assay for the detection of dermatophytes and optionally nondermatophytes in clinical specimens. Materials and methods We developed a two‐tube pan‐dermatophyte polymerase chain reaction (PCR) assay using six sloppy molecular beacon (SMB) probes. The first PCR uses dermatophyte‐specific primers and enables detection and i… Show more

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Cited by 11 publications
(9 citation statements)
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“…Additionally, supporters of modern contact methods can receive both the identification result and the prescription electronically, without the patient visiting the hospital or doctor's office again (Walser and Bosshard 2019). The result of molecular identification can be obtained on the day the sample reaches the laboratory or the next day, whereas fungal culture can take up to 1-3 weeks (Brillowska-Dabrowska et al 2010;Gnat et al 2017;Verrier and Monod 2017;Arastehfar et al 2019b;Walser and Bosshard 2019). The shortest time of 3 h from delivery of the material to obtaining the result is given in the method proposed by Miyajma et al (2013).…”
Section: Development Of a Diagnostic Pathmentioning
confidence: 99%
“…Additionally, supporters of modern contact methods can receive both the identification result and the prescription electronically, without the patient visiting the hospital or doctor's office again (Walser and Bosshard 2019). The result of molecular identification can be obtained on the day the sample reaches the laboratory or the next day, whereas fungal culture can take up to 1-3 weeks (Brillowska-Dabrowska et al 2010;Gnat et al 2017;Verrier and Monod 2017;Arastehfar et al 2019b;Walser and Bosshard 2019). The shortest time of 3 h from delivery of the material to obtaining the result is given in the method proposed by Miyajma et al (2013).…”
Section: Development Of a Diagnostic Pathmentioning
confidence: 99%
“…The culture positivity rate even in smear-positive specimens (resembling dermatophytes) is not more than 65-75%. 6 Flat, white, fastgrowing and expanding colonies with hyphae bundles in the periphery and slight yellowish-to-beige pigmentation in the center are typical for T. mentagrophytes of the Indian genotype [Figures 1a and b]. The reverse side of the colonies shows yellowish-to-beige and brown pigmentation [Figures 1c and d].…”
Section: Cultural Features Of Trichophyton Mentagrophytesmentioning
confidence: 99%
“…Sensitivity and specificity of PCR for detection of dermatophytes in clinical samples were estimated to be 96.9% and 90 4% for culture 46.7% and 98.7%, and for microscopy 91.4% and 84.0%, respectively. The detection of non-dermatophytes molds by PCR and culture did not correlate [33]. Table 4 summarises various studies comparing commercial kits versus in-house real time PCR techniques.…”
Section: Discussionmentioning
confidence: 99%