Publication:
Diagnosing infection with small ruminant lentiviruses of genotypes A and B by combining synthetic peptides in ELISA

dc.contributor.authorSanjosé, Leticiaes_ES
dc.contributor.authorCrespo, Helena
dc.contributor.authorGlaría Ezquer, Idoia
dc.contributor.authorAndrés Cara, Damián de
dc.contributor.authorReina Arias, Ramsés
dc.contributor.departmentIdAB. Instituto de Agrobiotecnología / Agrobioteknologiako Institutuaes_ES
dc.contributor.funderGobierno de Navarra / Nafarroako Gobernuaes
dc.contributor.funderUniversidad Pública de Navarra / Nafarroako Unibertsitate Publikoaes
dc.date.accessioned2020-09-16T11:21:48Z
dc.date.available2020-09-16T11:21:48Z
dc.date.issued2015
dc.description.abstractThe major challenges in diagnosing small ruminant lentivirus (SRLV) infection include early detection and genotyping of strains of epidemiological interest. A longitudinal study was carried out in Rasa Aragonesa sheep experimentally infected with viral strains of genotypes A or B from Spanish neurological and arthritic SRLV outbreaks, respectively. Sera were tested with two commercial ELISAs, three based on specific peptides and a novel combined peptide ELISA. Three different PCR assays were used to further assess infection status. The kinetics of anti-viral antibody responses were variable, with early diagnosis dependent on the type of ELISA used. Peptide epitopes of SRLV genotypes A and B combined in the same ELISA well enhanced the overall detection rate, whereas single peptides were useful for genotyping the infecting strain (A vs. B). The results of the study suggest that a combined peptide ELISA can be used for serological diagnosis of SRLV infection, with single peptide ELISAs useful for subsequent serotyping.en
dc.description.sponsorshipFunded by CICYT (AGL2010-22341-C04-01 and AGL2013-49137-C3-1R) and Navarra’s Government (IIQ010449.RI1 and IIQ14064.RI1). L. Sanjosé was a FPI-fellow of the Spanish MINECO and R. Reina had a contract of the Public University of Navarra.en
dc.format.extent28 p.
dc.format.mimetypeapplication/pdfen
dc.identifier.doi10.1016/j.tvjl.2015.01.012
dc.identifier.issn1090-0233
dc.identifier.urihttps://academica-e.unavarra.es/handle/2454/38131
dc.language.isoengen
dc.publisherElsevieren
dc.relation.ispartofThe Veterinary Journal, 2015, 204, 88-93en
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//AGL2013-49137-C3-1-R/ES/en
dc.relation.publisherversionhttps://doi.org/10.1016/j.tvjl.2015.01.012
dc.rights© 2015 Elsevier Ltd. This manuscript version is made available under the CC-BY-NC-ND 4.0.en
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen
dc.rights.accessRightsAcceso abierto / Sarbide irekiaes
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectSmall ruminant lentivirusen
dc.subjectGenotypeen
dc.subjectSerologyen
dc.subjectPeptide ELISAen
dc.titleDiagnosing infection with small ruminant lentiviruses of genotypes A and B by combining synthetic peptides in ELISAen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeArtículo / Artikuluaes
dc.type.versioninfo:eu-repo/semantics/acceptedVersionen
dc.type.versionVersión aceptada / Onetsi den bertsioaes
dspace.entity.typePublication
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relation.isAuthorOfPublicationb8d67008-109a-45c4-b632-218257bb3511
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relation.isAuthorOfPublication.latestForDiscoverye28c17f3-459d-4b77-9d08-2c325e7150da

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