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dc.contributor.authorGonzalez, Luis Miguel 
dc.contributor.authorBailo-Barroso, Begoña 
dc.contributor.authorFerrer, Elizabeth
dc.contributor.authorFernandez García, Maria D
dc.contributor.authorHarrison, Leslie Js
dc.contributor.authorParkhouse, Michael Re
dc.contributor.authorMcManus, Donald P
dc.contributor.authorGarate, Teresa 
dc.date.accessioned2019-01-31T10:22:55Z
dc.date.available2019-01-31T10:22:55Z
dc.date.issued2010-06-11
dc.identifier.citationParasit Vectors. 2010 Jun 11;3:51.es_ES
dc.identifier.issn1756-3305es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7042
dc.description.abstractA previously described Taenia saginata HDP2 DNA sequence, a 4-kb polymorphic fragment, was previously used as the basis for developing PCR diagnostic protocols for the species-specific discrimination of T. saginata from T. solium and for the differentiation of T. saginata from T. asiatica. The latter was shown subsequently to lack the required specificity, so we undertook genetic studies of the HDP2 sequence from T. saginata and T. asiatica to determine why, and to develop a novel HDP2-PCR protocol for the simultaneous unambiguous identification of human taeniids. Sequencing and further analysis of the HDP2 DNA fragments of 19 Asiatic isolates of T. saginata and T. asiatica indicated that the HDP2 sequences of both species exhibited clear genomic variability, due to polymorphic variable fragments, that could correspond to the non-transcribed region of ribosomal DNA. This newly observed polymorphism allowed us to develop a novel, reproducible and reliable HDP2-PCR protocol which permitted the simultaneous discrimination of all T. saginata and T. asiatica isolates examined. This species-specific identification was based on, and facilitated by, the clear size difference in amplicon profiles generated: fragments of 1300 bp, 600 bp and 300 bp were produced for T. asiatica, amplicons of 1300 bp and 300 bp being obtained for T. saginata. Control T. solium samples produced one amplicon of 600 bp with the HDP2-PCR protocol. The assay has the potential to prove useful as a diagnostic tool in areas such as South East Asia where T. saginata, T. asiatica and T. solium coexist.es_ES
dc.description.sponsorshipThis work was also supported by a grant from FIS (97/0141 and 00/407) and the Spanish Ministry of Science and Innovation and the Instituto de Salud Carlos III within the Network of Tropical Diseases Research (RICET RD06/0021/0019). L.M. Gonzalez was sponsored by fellowships from the ISCIII and RICET.es_ES
dc.language.isoenges_ES
dc.publisherBiomed Centrales_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleCharacterization of the Taenia spp HDP2 sequence and development of a novel PCR-based assay for discrimination of Taenia saginata from Taenia asiaticaes_ES
dc.typeArtículoes_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID20540755es_ES
dc.format.volume3es_ES
dc.format.number1es_ES
dc.format.page51es_ES
dc.identifier.doi10.1186/1756-3305-3-51es_ES
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.contributor.funderInstituto de Salud Carlos III - ISCIII
dc.description.peerreviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1186/1756-3305-3-51es_ES
dc.identifier.journalParasites & vectorses_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/97/0141es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/00/407es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD06/0021/0019es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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Atribución 4.0 Internacional
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