Genetic diversity and biochemical characteristics of Trichosporon asahii isolated from clinical specimens, houses of patients with summer-type-hypersensitivity pneumonitis, and environmental materials

• Published in: Journal of clinical microbiology 2001-07, Vol.39 (7), p.2405-2411
• Main Authors: SUGITA, Takashi, ICHIKAWA, Tomoe, MATSUKURA, Manami, SUEDA, Mika, TAKASHIMA, Masako, IKEDA, Reiko, NISHIKAWA, Akemi, SHINODA, Takako
• Format: Article
• Language: English
• Subjects: Alveolitis, Extrinsic Allergic - microbiology; Bacteriology; Biological and medical sciences; DNA, Fungal - analysis; DNA, Fungal - genetics; Environmental Microbiology; Epidemiology; Fundamental and applied biological sciences. Psychology; Genetic Variation - genetics; Housing; Humans; Microbiology; Molecular Sequence Data; Mycology; Mycoses - microbiology; Pathogenicity, host-agent relations, miscellaneous strains, epidemiology; Random Amplified Polymorphic DNA Technique; Sequence Analysis, DNA; Trichosporon - classification; Trichosporon - genetics; Trichosporon - isolation & purification; Trichosporon - metabolism; Trichosporon asahii; trichosporonosis
• ISSN: 0095-1137; 1098-660X
• DOI: 10.1128/JCM.39.7.2405-2411.2001

Trichosporon asahii, which is distributed in the environment, is the major causative agent of the opportunistic infection trichosporonosis, and it also causes summer-type hypersensitivity pneumonitis (SHP). Random amplification of polymorphic DNA analysis was used to determine the intraspecies diversity of 39 T. asahii isolates from clinical specimens, SHP patients' houses, and environmental materials. The three primers used revealed 46 polymorphic bands. A phenogram was generated by the unweighted pair-group method with arithmetic mean. Clinical isolates formed a cluster, characterized by a 90% matching coefficient, but they did not cluster with strains isolated from SHP patients' houses or environmental sources. In addition, the biochemical characteristics of 86 strains from three sources were examined with 31 compounds using an ID32C kit, and a phenogram was constructed. The phenogram consisted of three major clusters. Cluster I included most of the clinical SHP isolates, and cluster II included most of the environmental isolates. Cluster III contained only one strain. A remarkable difference was found in the abilities of the strains belonging to clusters I and II to utilize six compounds. These results suggest that the genetic diversity and biochemical characteristics of T. asahii seem to be related to the source of the isolate. We also found a specific DNA fragment for the clinical isolates and strains isolated from SHP patients' houses.