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Publicação:
Detection of Trypanosoma vivax using PCR and LAMP during aparasitemic periods

dc.contributor.authorCadioli, Fabiano Antonio [UNESP]
dc.contributor.authorFidelis Junior, Otavio Luiz [UNESP]
dc.contributor.authorSampaio, Paulo Henrique [UNESP]
dc.contributor.authorSantos, Giuliana Nascimento dos [UNESP]
dc.contributor.authorAndré, Marcos Rogério [UNESP]
dc.contributor.authorAlmeida Castilho, Kayo José Garcia de [UNESP]
dc.contributor.authorMachado, Rosangela Zacarias [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-12-07T15:37:33Z
dc.date.available2015-12-07T15:37:33Z
dc.date.issued2015-09-03
dc.description.abstractTrypanosoma vivax affects cattle herds in Africa and Americas and has been spreading rapidly in Brazil, through introduction of animals with subclinical infections and without apparent parasitemia, which makes its diagnosis challenging. PCR and LAMP are effective in detecting the presence of T. vivax DNA in situations of low parasitemia. LAMP is simpler and faster technique than PCR, and can be performed in the field, with limited resources. In this study, the capacities of conventional PCR and LAMP for detecting T. vivax in bovine blood samples classified as aparasitemic were evaluated. The capacity of conventional PCR (56.25%) for detecting positive samples was lower than that of LAMP (93.73%). This may influence the choice of screening tests for cattle herds infected with T. vivax.en
dc.description.affiliationFMVA, UNESP/Araçatuba, Rua Clóvis Pestana 793, 16050-470 Araçatuba, SP, Brazil.
dc.description.affiliationFCAV, UNESP/Jaboticabal, Via de Acesso Paulo Donato Castellane s/n, 14884-900 Jaboticabal, SP, Brazil.
dc.description.affiliationUnespFMVA, UNESP/Araçatuba, Rua Clóvis Pestana 793, 16050-470 Araçatuba, SP, Brazil.
dc.description.affiliationUnespFCAV, UNESP/Jaboticabal, Via de Acesso Paulo Donato Castellane s/n, 14884-900 Jaboticabal, SP, Brazil.
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2011/15945-5
dc.description.sponsorshipIdFAPESP: 2012/02284-3
dc.description.sponsorshipIdFAPESP: 2014/04066-9
dc.description.sponsorshipIdFAPESP: 2014/11600-1
dc.format.extent1-4
dc.identifierhttp://dx.doi.org/10.1016/j.vetpar.2015.09.001
dc.identifier.citationVeterinary Parasitology, p. 1-4, 2015.
dc.identifier.doi10.1016/j.vetpar.2015.09.001
dc.identifier.issn1873-2550
dc.identifier.lattes3884289076071083
dc.identifier.lattes9139899895580513
dc.identifier.pubmed26414906
dc.identifier.urihttp://hdl.handle.net/11449/131557
dc.language.isoeng
dc.publisherElsevier B. V.
dc.relation.ispartofVeterinary Parasitology
dc.rights.accessRightsAcesso restrito
dc.sourcePubMed
dc.subjectElisaen
dc.subjectLoop-mediated isothermal amplificationen
dc.subjectPolymerase chain reactionen
dc.subjectTrypanosomiasisen
dc.titleDetection of Trypanosoma vivax using PCR and LAMP during aparasitemic periodsen
dc.typeArtigo
dcterms.rightsHolderElsevier B. V.
dspace.entity.typePublication
unesp.author.lattes3884289076071083
unesp.author.lattes3254990612451836
unesp.author.lattes9139899895580513
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária, Araçatubapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Agrárias e Veterinárias, Jaboticabalpt
unesp.departmentPatologia Veterinária - FCAVpt
unesp.departmentClínica, Cirurgia e Reprodução Animal - FMVApt

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