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dc.contributor.authorFernandez-Baca, M.V.es_PE
dc.contributor.authorCastellanos-González, A.es_PE
dc.contributor.authorOre, R.A.es_PE
dc.contributor.authorAlccacontor-Munoz, J.L.es_PE
dc.contributor.authorHobán-Vergara, C.es_PE
dc.contributor.authorCastro, C.A.es_PE
dc.contributor.authorTanabe, M.B.es_PE
dc.contributor.authorMorales, M.L.es_PE
dc.contributor.authorOrtiz-Oblitas, P.es_PE
dc.contributor.authorWhite, A.C.es_PE
dc.contributor.authorCabada, M.M.es_PE
dc.date.accessioned2026-02-27T17:29:09Z
dc.date.available2026-02-27T17:29:09Z
dc.date.issued2024
dc.identifier.urihttp://hdl.handle.net/20.500.14074/9970
dc.description.abstractFasciola hepatica has a complex lifecycle with multiple intermediate and definitive hosts and influenced by environmental factors. The disease causes significant morbidity in children and its prevalent worldwide. There is lack of data about distribution and burden of the disease in endemic regions, owing to poor efficacy of the different diagnostic methods used. A novel PCR-based test was developed by using a portable mini-PCR® platform to detect Fasciola sp. DNA and interpret the results via a fluorescence viewer and smartphone image analyzer application. Human stool, snail tissue, and water samples were used to extract DNA. Primers targeting the ITS-1 of the 18S rDNA gene of Fasciola sp. were used. The limit of detection of the mini-PCR test was 1 fg/μL for DNA samples diluted in water, 10 fg/μL for Fasciola/snail DNA scramble, and 100 fg/μL for Fasciola/stool DNA scramble. The product detection by agarose gel, direct visualization, and image analyses showed the same sensitivity. The Fh mini-PCR had a sensitivity and specificity equivalent to real-time PCR using the same specimens. Testing was also done on infected human stool and snail tissue successfully. These experiments demonstrated that Fh mini-PCR is as sensitive and specific as real time PCR but without the use of expensive equipment and laboratory facilities. Further testing of multiple specimens with natural infection will provide evidence for feasibility of deployment to resource constrained laboratories.es_PE
dc.formatapplication/pdfes_PE
dc.language.isoenges_PE
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI).es_PE
dc.relation.ispartofurn:issn:20760817es_PE
dc.relation.ispartofhttps://www.scopus.com/pages/publications/85197158628es_PE
dc.relation.ispartofPathogens 2024; 13(6): 440es_PE
dc.rightsinfo:eu-repo/semantics/openAccesses_PE
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/es_PE
dc.subjectFasciola hepaticaes_PE
dc.subjectITS-1 genees_PE
dc.subjectRT-PCRes_PE
dc.subjectmini-PCRes_PE
dc.subjectmolecular diagnosticses_PE
dc.titleA PCR Test Using the Mini-PCR Platform and Simplified Product Detection Methods Is Highly Sensitive and Specific to Detect Fasciola hepatica DNA Mixed in Human Stool, Snail Tissue, and Water DNA Specimens.es_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_PE
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.03.07es_PE
dc.identifier.doihttps://doi.org/10.3390/pathogens13060440es_PE


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