Literature DB >> 8869498

Use of arbitrarily primed polymerase chain reaction to differentiate Trichophyton dermatophytes.

D Liu1, S Coloe, J Pedersen, R Baird.   

Abstract

Dermatophytes such as Trichophyton species are common human pathogens, the infection of which results in dermatophytosis (also known as ringworm). Several laboratory tests are used routinely for the diagnosis of dermatophytosis, but they are either slow or lacking specificity. Through examination of genomic DNA from Trichophyton dermatophytes and other fungi in arbitrarily primed PCR, it was shown that a random primer 5'-ACCCGACCTG-3' produced bands of 4.3 kb, 1.9 kb, 1.7 kb and 0.7 kb in T. rubrum DNA, bands of 2.5 kb, 1.9 kb and 0.8 kb in T. mentagrophytes var. interdigitale and T. mentagrophytes var. mentagrophytes DNA, and bands of 2.5 kb, 1.9 kb, 1.5 kb and 0.9 kb in T. tonsurans DNA. This primer amplified bands of different sizes in other fungal DNA. Therefore, based on the distinct band patterns observed in arbitrarily primed PCR using this primer, T. rubrum, T. mentagrophytes and T. tonsurans dermatophytes could be rapidly differentiated.

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Year:  1996        PMID: 8869498     DOI: 10.1111/j.1574-6968.1996.tb08040.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  16 in total

1.  Molecular markers reveal exclusively clonal reproduction in Trichophyton rubrum.

Authors:  Y Gräser; J Kühnisch; W Presber
Journal:  J Clin Microbiol       Date:  1999-11       Impact factor: 5.948

Review 2.  Strain differentiation of dermatophytes.

Authors:  Susan M Abdel-Rahman
Journal:  Mycopathologia       Date:  2008-05-14       Impact factor: 2.574

3.  Strain identification of Trichophyton rubrum by specific amplification of subrepeat elements in the ribosomal DNA nontranscribed spacer.

Authors:  C J Jackson; R C Barton; S L Kelly; E G Evans
Journal:  J Clin Microbiol       Date:  2000-12       Impact factor: 5.948

4.  Variation in restriction fragment length polymorphisms among serial isolates from patients with Trichophyton rubrum infection.

Authors:  A K Gupta; Y Kohli; R C Summerbell
Journal:  J Clin Microbiol       Date:  2001-09       Impact factor: 5.948

5.  Genotyping by RAPD-PCR analyses of Malassezia furfur strains from pityriasis versicolor and seborrhoeic dermatitis patients.

Authors:  Rinaldo F Gandra; Rita C G Simão; Flávia E Matsumoto; Bosco C M da Silva; Luciana S Ruiz; Eriques G da Silva; Walderez Gambale; Claudete R Paula
Journal:  Mycopathologia       Date:  2006-10       Impact factor: 2.574

6.  Molecular Strain Typing of Clinical Isolates, Trichophyton rubrum using Non Transcribed Spacer (NTS) Region as a Molecular Marker.

Authors:  Vijayakumar Ramaraj; Rajyoganandh S Vijayaraman; Elangovan Elavarashi; Sudha Rangarajan; Anupma Jyoti Kindo
Journal:  J Clin Diagn Res       Date:  2017-05-01

7.  Identification and genetic homogeneity of Trichophyton tonsurans isolated from several regions by random amplified polymorphic DNA.

Authors:  J A Kim; K Takizawa; K Fukushima; K Nishimura; M Miyaji
Journal:  Mycopathologia       Date:  1999       Impact factor: 2.574

8.  Identification and differentiation of Trichophyton rubrum clinical isolates using PCR-RFLP and RAPD methods.

Authors:  A Hryncewicz-Gwóźdź; T Jagielski; A Dobrowolska; J C Szepietowski; E Baran
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2011-03-18       Impact factor: 3.267

9.  Genotyping of Trichophyton rubrum by analysis of ribosomal-DNA intergenic spacer regions.

Authors:  Guoling Yang; Lijia An; Qiao Li; Jingrong Lin; Weida Liu; Liji Jin; Xiran Lin
Journal:  Mycopathologia       Date:  2007-06-07       Impact factor: 2.574

10.  Application of polymerase chain reaction (PCR) and PCR based restriction fragment length polymorphism for detection and identification of dermatophytes from dermatological specimens.

Authors:  R Bagyalakshmi; B Senthilvelan; K L Therese; S Murugusundram; H N Madhavan
Journal:  Indian J Dermatol       Date:  2008-01       Impact factor: 1.494

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