Mostrar el registro sencillo del ítem

dc.contributorFacultad de Veterinariaes_ES
dc.contributor.authorGómez-Casado, E.
dc.contributor.authorFregeneda Grandes, Juan Miguel 
dc.contributor.authorOlesen, Niels Jørgen
dc.contributor.authorLorenzen, Niels
dc.contributor.authorEstepa Pérez, Amparo
dc.contributor.authorColl Morales, Julio
dc.contributor.authorEncinas, Paloma
dc.contributor.otherSanidad Animales_ES
dc.date2011-03-15
dc.date.accessioned2019-04-22T23:21:49Z
dc.date.available2019-04-22T23:21:49Z
dc.date.issued2019-04-23
dc.identifier.citationFish and Shellfish Immunology, 2011, vol. 30, n. 3es_ES
dc.identifier.otherhttps://doi.org/10.1016/j.fsi.2011.01.021es_ES
dc.identifier.urihttp://hdl.handle.net/10612/10571
dc.descriptionP. 929-935es_ES
dc.description.abstractRainbow trout antibodies (Abs) binding to recombinant fragments (frgs) derived from the protein G of the viral haemorrhagic septicemia virus (VHSV)-07.71 strain, could be detected by ELISA (frg-ELISA) in sera from trout surviving laboratory-controlled infections. Abs were detected not only by using sera from trout infected with the homologous VHSV isolate but also with the VHSV-DK-201433 heterologous isolate, which had 13 amino acid changes. Sera from healthy trout and/or from trout surviving infectious haematopoietic necrosis virus (IHNV) infection, were used to calculate cut-off absorbances to differentiate negative from positive sera. Specific anti-VHSV Abs could then be detected by using any of the following frgs: frg11 (56-110), frg15 (65-250), frg16 (252-450) or G21-465. While high correlations were found among the ELISA values obtained with the different frgs, no correlations between any frg- ELISA and complement-dependent 50 % plaque neutralization test (PNT) titres could be demonstrated. Between 4 to 10 weeks after VHSV-infection, more trout sera were detected as positives by using heterologous frg-ELISA rather than homologous PNT. Furthermore, the percentage of positive sera detected by frg11-ELISA increased with time after infection to reach 100 %, while those detected by complement-dependent PNT decreased to 29.4 %, thus confirming that the lack of neutralising Abs does not mean the lack of any anti-VHSV Abs in survivor trout sera. Preliminary results with sera from field samples suggest that further refinements of the frg-ELISA could allow detection of anti-VHSV trout Abs in natural outbreaks caused by different heterologous VHSV isolates.The homologous frg-ELISA method could be useful to follow G immunization attempts during vaccine development and/or to best understand the fish Ab response during VHSV infections. The viral frgs approach might also be used with other fish species and/or viruses.es_ES
dc.languageenges_ES
dc.publisherElsevieres_ES
dc.subjectInmunologíaes_ES
dc.subjectSanidad animales_ES
dc.subjectVeterinariaes_ES
dc.subjectZoologíaes_ES
dc.subject.otherTruchases_ES
dc.subject.otherInmunoglobulinases_ES
dc.subject.otherSerologíaes_ES
dc.titleRainbow trout surviving infections of viral haemorrhagic septicemia virus (vhsv) show lasting antibodies to recombinant g protein fragmentses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.description.peerreviewedSIes_ES


Ficheros en el ítem

Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem