Publication:
Comparative assessment of ELISAs using recombinant saposin-like protein 2 and recombinant cathepsin L-1 from Fasciola hepatica for the serodiagnosis of human Fasciolosis

dc.contributor.authorGottstein, Bruno
dc.contributor.authorSchneeberger, Marianne
dc.contributor.authorBoubaker, Ghalia
dc.contributor.authorMerkle, Bernadette
dc.contributor.authorHuber, Cristina
dc.contributor.authorSpiliotis, Markus
dc.contributor.authorMüller, Norbert
dc.contributor.authorGarate, Teresa
dc.contributor.authorDoherr, Marcus G
dc.date.accessioned2018-12-19T10:44:33Z
dc.date.available2018-12-19T10:44:33Z
dc.date.issued2014-06-12
dc.description.abstractTwo recombinant Fasciola hepatica antigens, saposin-like protein-2 (recSAP2) and cathepsin L-1 (recCL1), were assessed individually and in combination in enzyme-linked immunosorbent assays (ELISA) for the specific serodiagnosis of human fasciolosis in areas of low endemicity as encountered in Central Europe. Antibody detection was conducted using ProteinA/ProteinG (PAG) conjugated to alkaline phosphatase. Test characteristics as well as agreement with results from an ELISA using excretory-secretory products (FhES) from adult stage liver flukes was assessed by receiver operator characteristic (ROC) analysis, specificity, sensitivity, Youdens J and overall accuracy. Cross-reactivity was assessed using three different groups of serum samples from healthy individuals (n=20), patients with other parasitic infections (n=87) and patients with malignancies (n=121). The best combined diagnostic results for recombinant antigens were obtained using the recSAP2-ELISA (87% sensitivity, 99% specificity and 97% overall accuracy) employing the threshold (cut-off) to discriminate between positive and negative reactions that maximized Youdens J. The findings showed that recSAP2-ELISA can be used for the routine serodiagnosis of chronic fasciolosis in clinical laboratories; the use of the PAG-conjugate offers the opportunity to employ, for example, rabbit hyperimmune serum for the standardization of positive controls.es_ES
dc.description.peerreviewedes_ES
dc.format.number6es_ES
dc.format.pagee2860es_ES
dc.format.volume8es_ES
dc.identifier.citationPLoS Negl Trop Dis. 2014 Jun 12;8(6):e2860es_ES
dc.identifier.doi10.1371/journal.pntd.0002860es_ES
dc.identifier.e-issn1935-2735es_ES
dc.identifier.issn1935-2735es_ES
dc.identifier.journalPLoS neglected tropical diseaseses_ES
dc.identifier.pubmedID24922050es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/6899
dc.language.isoenges_ES
dc.publisherPublic Library of Science (PLOS)
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pntd.0002860es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiología (CNM)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAdolescentes_ES
dc.subject.meshAdultes_ES
dc.subject.meshAgedes_ES
dc.titleComparative assessment of ELISAs using recombinant saposin-like protein 2 and recombinant cathepsin L-1 from Fasciola hepatica for the serodiagnosis of human Fasciolosises_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication3d704a19-fdd1-4b31-97da-1c2cd59180d1
relation.isAuthorOfPublication.latestForDiscovery3d704a19-fdd1-4b31-97da-1c2cd59180d1
relation.isPublisherOfPublicationa2759e3d-0d58-4e8a-9fcd-c6130ee333d1
relation.isPublisherOfPublication.latestForDiscoverya2759e3d-0d58-4e8a-9fcd-c6130ee333d1

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