Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/1417
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dc.contributor.authorJimenez-Coello, Matildeen_US
dc.contributor.authorShelite, Thomasen_US
dc.contributor.authorCastellanos-Gonzalez, Alejandroen_US
dc.contributor.authorSaldarriaga, Omaren_US
dc.contributor.authorRivero, Rocioen_US
dc.contributor.authorOrtega-Pacheco, Antonioen_US
dc.contributor.authorAcevedo-Arcique, Carlosen_US
dc.contributor.authorAmaya-Guardia, Karlaen_US
dc.contributor.authorGarg, Nishaen_US
dc.contributor.authorMelby, Peteren_US
dc.contributor.authorTravi, Bruno Len_US
dc.date.accessioned2019-11-29T20:13:40Z-
dc.date.available2019-11-29T20:13:40Z-
dc.date.issued2018-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/1417-
dc.description.abstractChagas disease is a lingering Public Health problem in Latin America with ∼5.7 million people infected with Trypanosoma cruzi. Transmission is still taking place in most countries of the Americas, including the United States. Dogs are frequently infected with T. cruzi and its high infection prevalence is associated with increased risk of Chagas disease in humans. The city of Mérida in the Yucatan peninsula is endemic for Chagas disease and canines are frequently infected with T. cruzi. The objective of this study was to evaluate the performance of a qualitative point of care (POC) molecular test (RPA-LF, recombinase polymerase amplification-lateral flow) developed in our laboratory for identifying infected dogs. We used retrospective samples of dogs that came for consultation because of cardiac alterations and proved to be infected with T. cruzi as determined by enzyme-linked immunosorbent assay (ELISA), Western blot, and quantitative PCR (qPCR). The analytical sensitivity indicated that RPA-LF amplified T. cruzi DNA in samples containing almost equal to one to two parasites per reaction. Serial twofold dilutions of T. cruzi epimastigotes showed that the test had 95% (19/20) repeatability at concentrations of two parasites per reaction. The test showed no cross reactivity with human DNA or other protozoan parasites (Trypanosoma rangeli, Leishmania spp., and Plasmodium spp.). RPA-LF had the capacity to amplify all discrete typing units (DTUs I-VI) of T. cruzi that circulate in domestic or extradomestic environments. The RPA-LF had 93.2% (95% confidence interval 87.2-98.1) sensitivity and excellent agreement with qPCR used as gold standard (Cohen's Kappa test = 0.963). ELISA was positive in 96.6% (85/88) of dogs, which together with the molecular tests confirmed the frequent contact with infected triatomine bugs in the city of Mérida. These preliminary results on the diagnostic efficacy of the RPA-LF deserve further large-scale field testing of this POC test for T. cruzi infection in endemic areas.en_US
dc.language.isoenen_US
dc.relation.ispartofVector borne and zoonotic diseases (Larchmont, N.Y.)en_US
dc.subjectMexicoen_US
dc.subjectEnfermedad de Chagasen_US
dc.subjectTrypanosoma cruzien_US
dc.subjectDiagnósticoen_US
dc.subjectPerrosen_US
dc.subjectPrueba molecularen_US
dc.titleEfficacy of Recombinase Polymerase Amplification to Diagnose Trypanosoma cruzi Infection in Dogs with Cardiac Alterations from an Endemic Area of Mexicoen_US
dc.title.alternativeEficacia de la amplificación de la polimerasa con recombinasa para diagnosticar la infección por Trypanosoma cruzi en perros con alteraciones cardíacas en un área endémica de México.en_US
dc.typeArtículoen_US
dc.identifier.doi10.1089/vbz.2017.2258-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArtículo-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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