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dc.contributor.authorCura, Carolina I.es_ES
dc.contributor.authorDuffy, Tomases_ES
dc.contributor.authorLucero, Raúl H.es_ES
dc.contributor.authorBisio, Margaritaes_ES
dc.contributor.authorPéneau, Juliees_ES
dc.contributor.authorJiménez-Coello, Matildees_ES
dc.contributor.authorCalabuig, Evaes_ES
dc.contributor.authorGiménez, María J.es_ES
dc.contributor.authorValencia Ayala, Edwardes_ES
dc.contributor.authorKjos, Sonia A.es_ES
dc.contributor.authorSantalla, Josées_ES
dc.contributor.authorMahaney, Susan M.es_ES
dc.contributor.authorCayo, Nelly M.es_ES
dc.contributor.authorNagel, Claudiaes_ES
dc.contributor.authorBarcán, Lauraes_ES
dc.contributor.authorMálaga Machaca, Edith S.es_ES
dc.contributor.authorAcosta Viana, Karla Y.es_ES
dc.contributor.authorBrutus, Laurentes_ES
dc.contributor.authorOcampo, Susana B.es_ES
dc.contributor.authorAznar, Christinees_ES
dc.contributor.authorCuba Cuba, César A.es_ES
dc.contributor.authorGürtler, Ricardo E.es_ES
dc.contributor.authorRamsey, Janine M.es_ES
dc.contributor.authorRibeiro, Isabelaes_ES
dc.contributor.authorVandeBerg, John L.es_ES
dc.contributor.authorYadon, Zaida E.es_ES
dc.contributor.authorOsuna Carrillo De Albornoz, Antonio es_ES
dc.contributor.authorSchijman, Alejandro G.es_ES
dc.date.accessioned2015-06-22T07:50:24Z
dc.date.available2015-06-22T07:50:24Z
dc.date.issued2015
dc.identifier.citationCura, C.I.; et al. Multiplex Real-Time PCR Assay Using TaqMan Probes for the Identification of Trypanosoma cruzi DTUs in Biological and Clinical Samples. Plos One Neglected Tropical Diseases, 9(5): e0003765 (2015). [doi: 10.1371/journal.pntd.0003765]es_ES
dc.identifier.issn1935-2735
dc.identifier.urihttp://hdl.handle.net/10481/36691
dc.description.abstractBackground: Trypanosoma cruzi has been classified into six Discrete Typing Units (DTUs), designated as TcI–TcVI. In order to effectively use this standardized nomenclature, a reproducible genotyping strategy is imperative. Several typing schemes have been developed with variable levels of complexity, selectivity and analytical sensitivity. Most of them can be only applied to cultured stocks. In this context, we aimed to develop a multiplex Real-Time PCR method to identify the six T. cruzi DTUs using TaqMan probes (MTq-PCR).en_EN
dc.description.abstractMethods/Principal Findings: The MTq-PCR has been evaluated in 39 cultured stocks and 307 biological samples from vectors, reservoirs and patients from different geographical regions and transmission cycles in comparison with a multi-locus conventional PCR algorithm. The MTq-PCR was inclusive for laboratory stocks and natural isolates and sensitive for direct typing of different biological samples from vectors, reservoirs and patients with acute, congenital infection or Chagas reactivation. The first round SL-IR MTq-PCR detected 1 fg DNA/reaction tube of TcI, TcII and TcIII and 1 pg DNA/reaction tube of TcIV, TcV and TcVI reference strains. The MTq-PCR was able to characterize DTUs in 83% of triatomine and 96% of reservoir samples that had been typed by conventional PCR methods. Regarding clinical samples, 100% of those derived from acute infected patients, 62.5% from congenitally infected children and 50% from patients with clinical reactivation could be genotyped. Sensitivity for direct typing of blood samples from chronic Chagas disease patients (32.8% from asymptomatic and 22.2% from symptomatic patients) and mixed infections was lower than that of the conventional PCR algorithm.en_EN
dc.description.abstractConclusions/Significance: Typing is resolved after a single or a second round of Real-Time PCR, depending on the DTU. This format reduces carryover contamination and is amenable to quantification, automation and kit production.en_EN
dc.description.sponsorshipThis work received financial support from the Ministry of Science and Technology of Argentina [PICT 2011-0207 to AGS] and the National Scientific and Technical Research Council in Argentina (CONICET) [PIP 112 2011-010-0974 to AGS]. Work related to evaluation of biological samples was partially sponsored by the Pan-American Health Organization (PAHO) [Small Grants Program PAHO-TDR]; the Drugs and Neglected Diseases Initiative (DNDi, Geneva, Switzerland), Wellcome Trust (London, United Kingdom), SANOFI-AVENTIS (Buenos Aires, Argentina) and the National Council for Science and Technology in Mexico (CONACYT) [FONSEC 161405 to JMR].en_EN
dc.language.isoenges_ES
dc.publisherPublic Library of Science (PLOS)es_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Licensees_ES
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Españaen_EN
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/en_EN
dc.subjectTrypanosoma cruzien_EN
dc.subjectPolymerase chain reactionen_EN
dc.subjectGenotypingen_EN
dc.subjectChagas diseaseen_EN
dc.subjectLeishmaniaen_EN
dc.subjectVector-borne diseasesen_EN
dc.subjectSequence databasesen_EN
dc.subjectParasitic diseases en_EN
dc.titleMultiplex Real-Time PCR Assay Using TaqMan Probes for the Identification of Trypanosoma cruzi DTUs in Biological and Clinical Samplesen_EN
dc.typejournal articleen_EN
dc.rights.accessRightsopen accessen_EN
dc.identifier.doi10.1371/journal.pntd.0003765


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