2021
DOI: 10.1055/s-0041-1731111
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Strain Typing of Trichosporon asahii Clinical Isolates by Random Amplification of Polymorphic DNA (RAPD) Analysis

Abstract: Objective The aim of this study was to identify and isolate Trichosporon asahii (T. asahii) from clinical samples and to assess the genetic relatedness of the most frequently isolated strains of T. asahii using random amplification of polymorphic DNA (RAPD) primers GAC-1 and M13. Methods All the clinical samples that grew Trichosporon species, identified and confirmed by polymerase chain reaction (PCR) using Trichosporon genus-specific primers, were considered for the study. Confirmation of the species T. asah… Show more

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“…The primer used in RAPD-PCR was primer 272 (59-AGCGGGCCAA-39). 11 The amplification volume was 20 mL, which included 2 mL primers (100 mmol/L), 10 mL 23 PowerTaq PCR Master Mix, 1.5 mL template, and 6.5 mL double-distilled H 2 O. The parameters of RAPD-PCR were as follows: 4 cycles of 5 minutes at 94 C, 5 minutes at 36 C, and 5 minutes at 72 C; 30 cycles of 1 minute at 94 C, 1 minute at 36 C, and 2 minutes at 72 C; and a final extension at 72 C for 10 minutes.…”
Section: Methodsmentioning
confidence: 99%
“…The primer used in RAPD-PCR was primer 272 (59-AGCGGGCCAA-39). 11 The amplification volume was 20 mL, which included 2 mL primers (100 mmol/L), 10 mL 23 PowerTaq PCR Master Mix, 1.5 mL template, and 6.5 mL double-distilled H 2 O. The parameters of RAPD-PCR were as follows: 4 cycles of 5 minutes at 94 C, 5 minutes at 36 C, and 5 minutes at 72 C; 30 cycles of 1 minute at 94 C, 1 minute at 36 C, and 2 minutes at 72 C; and a final extension at 72 C for 10 minutes.…”
Section: Methodsmentioning
confidence: 99%