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. 2013 Jan;51(1):295–298. doi: 10.1128/JCM.02221-12

Fig 1.

Fig 1

Specificity verification of the Trichosporon spp. PNA probe and assessments of rRNA retention and its hybridizability in experimentally infected mice. (A) ISH using the Trichosporon spp. PNA probe in renal tissue from mice infected with T. asahii. Strong positive signals against 28S rRNA of Trichosporon spp. were observed in the specimen. (B) ISH using the Trichosporon spp. PNA probe in renal tissue from mice infected with C. albicans. Positive signals were not observed in the specimen. (C) ISH result with the panfungal PNA probe in renal tissue from mice infected with T. asahii. Strong positive signals were observed in the specimen. (D) ISH result with the panfungal PNA probe in renal tissue from mice infected with C. albicans. Strong positive signals were observed in the specimen. Magnification, ×400.