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Journal of Clinical Microbiology, October 2003, p. 4583-4588, Vol. 41, No. 10
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.10.4583-4588.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Restriction Fragment Length Polymorphism Analysis of Ribosomal DNA Intergenic Regions Is Useful for Differentiating Strains of Trichophyton mentagrophytes

Takashi Mochizuki,1* Hiroshi Ishizaki,1 Richard C. Barton,2 Mary K. Moore,3 Colin J. Jackson,4 Steven L. Kelly,4 and E. Glyn V. Evans5

Department of Dermatology, Kanazawa Medical University, Uchinada, Japan,1 Division of Microbiology, University of Leeds, Leeds,2 Department of Medical Mycology, St. Johns Institute of Dermatology, Kings College, London,3 Institute of Biological Sciences, University of Wales, Aberystwyth,4 Welsh Mycology Reference Laboratory, Public Health Laboratory, Cardiff, United Kingdom5

Received 17 June 2002/ Accepted 17 July 2003

Twenty isolates of Tricophyton mentagrophytes var. mentagrophytes and 47 isolates of T. mentagrophytes var. interdigitale, identified by morphological characteristics, were screened by restriction fragment length polymorphism (RFLP) analysis of the PCR-amplified internal transcribed spacer (ITS) region of ribosomal DNA (rDNA). Sixty isolates (14 of 20 T. mentagrophytes var. mentagrophytes isolates and 46 of 47 T. mentagrophytes var. interdigitale isolates) shared an identical ITS RFLP profile and were further investigated by using a probe targeted to the rDNA nontranscribed spacer (NTS) region. Polymorphisms were observed in the NTS regions of both T. mentagrophytes var. mentagrophytes and T. mentagrophytes var. interdigitale isolates. Twenty-three individual RFLP patterns (DNA types P-1 to P-12 and A-1 to A-11) were recognized and divided into two groups depending on the presence (P) or absence (A) of a 2.5-kb band, which correlated to a large extent with the morphological variety. Eleven of 14 T. metagrophytes var. mentagrophytes isolates were A types, and all of the 46 T. mentagrophytes var. interdigitale isolates were P types. A majority of strains (23 of 60 [38.3%]) were characterized by one RFLP pattern (pattern P-1), and eight types (P-1 to P-6, P-8, and P-9) accounted for 75% (45 of 60) of all strains, including all of the T. mentagrophytes var. interdigitale isolates. The remaining 15 types were represented by one only isolate and included all of the T. mentagrophytes var. mentagrophytes isolates. We conclude that RFLP analysis of the rDNA NTS region is a valuable technique for differentiation of T. mentagrophytes strains. Furthermore, by use of this method, there appears to be a greater degree of diversity among T. mentagrophytes var. mentagrophytes isolates than among T. mentagrophytes var. interdigitale isolates.


* Corresponding author. Mailing address: Department of Dermatology, Kanazawa Medical University, Uchinada, Japan. Phone: 81 76 286 2211. Fax: 81 76 286 6369. E-mail: mocizuki{at}kanazawa-med.ac.jp.


Journal of Clinical Microbiology, October 2003, p. 4583-4588, Vol. 41, No. 10
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.10.4583-4588.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




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