dc.creator | Gaviria Camino, Marcela | |
dc.creator | Rivera Arango, Vanessa | |
dc.creator | Muñoz Cadavid, Cesar | |
dc.creator | Cano Restrepo, Luz Elena | |
dc.creator | Naranjo Preciado, Tonny Williams | |
dc.date | 2021-07-28T02:44:23Z | |
dc.date | 2021-07-28T02:44:23Z | |
dc.date | 2015 | |
dc.date.accessioned | 2023-08-28T19:52:32Z | |
dc.date.available | 2023-08-28T19:52:32Z | |
dc.identifier | 1413-8670 | |
dc.identifier | http://hdl.handle.net/10495/21203 | |
dc.identifier | 10.1016/j.bjid.2015.04.008 | |
dc.identifier | 1678-4391 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/8470070 | |
dc.description | 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. | |
dc.description | COL0013709 | |
dc.format | 8 | |
dc.format | application/pdf | |
dc.format | application/pdf | |
dc.language | eng | |
dc.publisher | Brazilian Society of Infectious Diseases | |
dc.publisher | Micología Médica y Experimental | |
dc.publisher | Salvador, Brasil | |
dc.relation | Braz. J. Infect. Dis. | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/2.5/co/ | |
dc.rights | http://purl.org/coar/access_right/c_abf2 | |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Paracoccidioidomicosis | |
dc.subject | Paracoccidioidomycosis | |
dc.subject | Reacción en Cadena de la Polimerasa | |
dc.subject | Polymerase Chain Reaction | |
dc.subject | Diagnóstico molecular | |
dc.subject | Paracoccidioides brasiliensis | |
dc.subject | http://aims.fao.org/aos/agrovoc/c_34079 | |
dc.title | Validation and clinical application of a nested PCR for paracoccidioidomycosis diagnosis in clinical samples from Colombian patients | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:eu-repo/semantics/publishedVersion | |
dc.type | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.type | https://purl.org/redcol/resource_type/ART | |
dc.type | Artículo de investigación | |