dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
dc.contributorUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T14:03:45Z
dc.date.available2014-05-20T14:03:45Z
dc.date.created2014-05-20T14:03:45Z
dc.date.issued2008-03-01
dc.identifierJournal of Virological Methods. Amsterdam: Elsevier B.V., v. 148, n. 1-2, p. 283-285, 2008.
dc.identifier0166-0934
dc.identifierhttp://hdl.handle.net/11449/22420
dc.identifier10.1016/j.jviromet.2007.11.005
dc.identifierWOS:000254720500038
dc.description.abstractSequences of the coat protein amino acids of definitive and tentative species of carlaviruses deposited in GenBank were aligned and a region of seven amino acids (GLGVPTE) was found to be conserved. The corresponding nucleotides were aligned, allowing the design of a degenerate primer that together with an oligo dT anti-sense primer, was effective for the detection of three distinct carlavirus species, two transmitted by aphids and one by whitefly. These primers have the advantage that about 940 nt from the 3'-terminus, comprising part of the CP gene (about 60%), the 11 K gene, and the terminal untranslated region can be amplified for sequencing. The fact that this amino acid sequence is conserved in almost all of the sequenced carlaviruses, allows the prediction that this primer pair will be useful as a diagnostic tool for carlavirus species. (C) 2007 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationJournal of Virological Methods
dc.relation1.756
dc.relation0,858
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectcarlavirus identification
dc.subjectdiagnosis
dc.subjectFlexiviridae
dc.subjectRT-PCR
dc.titleA degenerate primer allows amplification of part of the 3 '-terminus of three distinct carlavirus species
dc.typeArtículos de revistas


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