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Published on: October 24, 2013
Genotypic study of strains belonging to the genus Trichosporon
S Carnovale1, J Lorenzo, S Kaufman
1Centro de Micología, Dep de Microbiología, Facultad de Medicina, Universidad de Buenos Aires, Paraguay. susacarnov@yahoo.com.ar
Abstract:
Trichosporon asahii is an opportunistic fungus considered the leading etiologic agent of trichospornosis, a disease that causes great morbidity/mortality among affected patients. The identification of the etiologic agent is generally obtained through physiological and morphological studies. Molecular investigations, such as species-specific primers (PCR), have recently been developed with the aim of applying a more simple, specific, and faster technology for mycological diagnosis. The genetic material amplification technique using ad-random primers (RAPD: random amplified polymorphic DNA) is an epidemiological tool which enables research on infection by and transmission of suspected agents. In this study, the amplified polymorphic DNA technique was used to determine the intraspecific diversity of 10 Trichosporon asahii strains. Primers OPAO-15 and 1821 were used and these allowed association to 5 and 3 electrophoretic patterns, respectively. The T. asahii molecular identification, which had been previously analyzed by conventional methods, was performed by means of primers TAAF and pITS4. Our results support the use of these techniques for clonality studies of the strains of this fungus as well as for the fast and specific identification of its members in clinical cases.
Insights
This study utilized random amplified polymorphic DNA (RAPD) to analyze genetic diversity within Trichosporon asahii strains. The findings support RAPD as a valuable tool for fungal clonality studies and rapid clinical identification.
Area of Science:
- Medical Mycology
- Molecular Biology
- Epidemiology
Background:
- Trichosporon asahii is a significant opportunistic fungal pathogen causing trichosporonosis, a disease with high morbidity and mortality.
- Traditional identification methods for T. asahii rely on physiological and morphological characteristics, which can be time-consuming.
- Molecular techniques, including PCR and RAPD, offer faster and more specific diagnostic approaches.
Purpose of the Study:
- To determine the intraspecific genetic diversity among 10 Trichosporon asahii strains.
- To evaluate the utility of random amplified polymorphic DNA (RAPD) for analyzing T. asahii clonality.
- To assess the efficacy of specific primers for rapid and accurate molecular identification of T. asahii.
Main Methods:
- Random Amplified Polymorphic DNA (RAPD) technique was employed to analyze 10 T. asahii strains.
- Specific primers OPAO-15 and 1821 were used for RAPD analysis, generating distinct electrophoretic patterns.
- Conventional methods and species-specific primers (TAAF and pITS4) were used for molecular identification.
Main Results:
- RAPD primers OPAO-15 and 1821 differentiated T. asahii strains, yielding 5 and 3 distinct electrophoretic patterns, respectively.
- Molecular identification using primers TAAF and pITS4 confirmed previous conventional analyses.
- The study demonstrated the potential for RAPD to assess clonality and differentiate strains of T. asahii.
Conclusions:
- Random amplified polymorphic DNA (RAPD) is effective for studying the clonality of Trichosporon asahii strains.
- Molecular techniques, including RAPD and specific primers, enable fast and accurate identification of T. asahii in clinical settings.
- These molecular tools enhance mycological diagnosis and epidemiological investigations of trichosporonosis.
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