Validation and clinical application of a nested PCR for paracoccidioidomycosis diagnosis in clinical samples from Colombian patients
ABSTRACT: Paracoccidioidomycosis is a systemic and endemic mycosis, restricted to tropical and sub-tropical areas of Latin America. The infection is caused by the thermal dimorphic fungusParacoccidioides brasiliensis and Paracoccidioides lutzii. The diagnosis of paracoccidioidomyco-sis is usually pe...
- Autores:
-
Gaviria Camino, Marcela
Rivera Arango, Vanessa
Muñoz Cadavid, Cesar
Cano Restrepo, Luz Elena
Naranjo Preciado, Tonny Williams
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2015
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/21203
- Acceso en línea:
- http://hdl.handle.net/10495/21203
- Palabra clave:
- Paracoccidioidomicosis
Paracoccidioidomycosis
Reacción en Cadena de la Polimerasa
Polymerase Chain Reaction
Diagnóstico molecular
Paracoccidioides brasiliensis
http://aims.fao.org/aos/agrovoc/c_34079
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc-nd/2.5/co/
Summary: | ABSTRACT: Paracoccidioidomycosis is a systemic and endemic mycosis, restricted to tropical and sub-tropical areas of Latin America. The infection is caused by the thermal dimorphic fungusParacoccidioides brasiliensis and Paracoccidioides lutzii. The diagnosis of paracoccidioidomyco-sis is usually performed by microscopic examination, culture and immunodiagnostic teststo respiratory specimens, body fluids and/or biopsies; however these methods require labo-ratory personnel with experience and several days to produce a result. In the present study,we have validated and evaluated a nested PCR assay targeting the gene encoding the Para-coccidioides gp43 membrane protein in 191 clinical samples: 115 samples from patients withproven infections other than paracoccidioidomycosis, 51 samples as negative controls, and25 samples from patients diagnosed with paracoccidioidomycosis. Additionally, the speci-ficity of the nested PCR assay was also evaluated using purified DNA isolated from culturesof different microorganisms (n = 35) previously identified by culture and/or sequencing. Theresults showed that in our hands, this nested PCR assay for gp43 protein showed specificityand sensitivity rates of 100%. The optimized nested PCR conditions in our laboratory alloweddetection down to 1 fg of P. brasiliensis DNA. |
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