Literature DB >> 17644713

Microsatellite markers reveal geographic population differentiation in Trichophyton rubrum.

Yvonne Gräser1, Janine Fröhlich1, Wolfgang Presber1, Sybren de Hoog2.   

Abstract

A worldwide selection of more than 200 isolates of the anthropophilic dermatophyte Trichophyton rubrum were analysed using seven microsatellite markers. Fifty-five multilocus genotypes were recognized, allowing a subdivision of the species into two populations. Both populations reproduced strictly clonally, showed a different predilection on the human host (scalp vs foot) and displayed geographic differentiation. Genotypes of one population originated predominantly from Africa, whilst the second population showed a worldwide distribution excluding the African continent. Genotypic diversity was highest in the African population, despite the lower number of strains analysed, suggesting that T. rubrum is likely to have evolved in Africa. No diagnostic correlation was observed between multilocus genotypes and any of the phenotypical characteristics of the strains. The involvement of multiple strains in a single patient detected by workers using other typing methods was not supported by these microsatellite markers. Four of the developed microsatellite markers may be applied for diagnostic purposes.

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Year:  2007        PMID: 17644713     DOI: 10.1099/jmm.0.47138-0

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  20 in total

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

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Journal:  Eukaryot Cell       Date:  2008-02-22

8.  Molecular Markers Useful for Intraspecies Subtyping and Strain Differentiation of Dermatophytes.

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Journal:  Mycopathologia       Date:  2016-07-25       Impact factor: 2.574

9.  Mating type gene (MAT1-1) in Japanese isolates of Trichophyton rubrum.

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10.  Rapid identification and differentiation of Trichophyton species, based on sequence polymorphisms of the ribosomal internal transcribed spacer regions, by rolling-circle amplification.

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Journal:  J Clin Microbiol       Date:  2008-01-30       Impact factor: 5.948

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