Abstract:We performed a cluster analysis of human and animal pathogenic Microsporum species and their teleomorphic states, Arthroderma species, including A. otae-related species (M. canis, M. audouinii, M. distortum, M. equinum, M. langeronii, and M. ferrugineum) and M. gypseum complex (A. fulvum, A. gypseum, and A. incurvatum) using DNA sequences of nuclear ribosomal internal transcribed spacer 1 (ITS1). The dendrogram showed the members of A. otae-related species to be monophyletic and to construct an extremely closely related cluster with a long horizontal branch. This ITS1-homologous group of A. otae was organized in 6 unique genotypes, while sequences of the members of the ITS J-homologous group of M. gypseum complex are more diverse. This ITS I-based database of Microsporum species and their teleomorphic states will provide a useful and reliable species identification system: it is time-saving (takes two to three days), accurate and applicable even to strains with atypical morphological features or in a non-culturable state.Key words: Microsporum species,Arthroderma species, Internal transcribed spacer 1, DNA sequences Microsporum species are important members of the dermatophytes (filamentous fungi, classified as Euascomycetes and consisting of the genera Microsporum, Trichophyton and Epidermophyton), which have the capacity to invade keratinized tissues of humans and other animals to produce an infection, dermatophytosis (9,16,29 Specific DNA sequences of internal transcribed spacer 1 (ITS I) of ribosomal DNA in the human and animal pathogenic Microsporum species and their teleomorphic states, Arthroderma species, were therefore determined and a cluster analysis performed. ITS I is located between the 18S and 5.8S rONA. As reported previously, the variable ITS regions have been proven useful in resolving relationships between close taxonomic relatives (3), and in the field of medical mycology several phylogenetic studies using the ITS I region were recently documented (1,20,27,28). The authors have reported that it is feasible to successfully perform species identification and/or strain typing of Trichophyton species (the major dermatophytes; 2, 19, 22), which are hard to identify from their morphological features, by demonstrating their dendrogram using a base pair sequence Abbreviations: AFLP, amplified fragment length polymorphism; EDTA, ethylenediaminetetraacetic acid; ITS, internal transcribed spacer; peR, polymerase chain reaction; RAPD, random amplificationof polymorphic DNA; SDA, Sabourauddextrose agar.