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dc.contributor.authorKrasnov, Aleksei
dc.contributor.authorAfanasyev, Sergey
dc.contributor.authorNylund, Stian
dc.contributor.authorRebl, Alexander
dc.date.accessioned2021-01-27T14:16:01Z
dc.date.available2021-01-27T14:16:01Z
dc.date.created2020-11-11T20:30:02Z
dc.date.issued2020
dc.identifier.citationGenes. 2020, 11 (11), 1-11.
dc.identifier.issn2073-4425
dc.identifier.urihttps://hdl.handle.net/11250/2725015
dc.description.abstractWe report the development of a multigene gene expression assay on the BioMark HD platform for the evaluation of immune competence (ImCom) in farmed Atlantic salmon. The first version of the assay included 92 genes selected on the basis of transcriptome analyses in 54 trials that challenged the immune system; annotations were taken into account to represent the key pathways of innate and adaptive immunity. ImCom was tested on samples collected from seven independent projects. Fish were reared from the start feeding to eight months in the sea at eight units in different parts of Norway. Several tissues were analyzed. Linear discriminant analysis (LDA) showed that no more than 10 genes were required to separate groups, and a set of 46 immune genes was sufficient for any task. The second version of the assay was tested in the gills of two groups of high-performing healthy smolts and in groups with intermediate and high mortality rates (IM and HM, respectively). A set of 645 gill samples from clinically healthy Atlantic salmon was used as a reference. The IM group showed general suppression of immunity. All HM group salmon were above the threshold by the squared deviation from the reference. This group showed marked upregulation of genes involved in acute stress and inflammation: mmp-9, mmp-13, hsp70, il-1b, lect2, and cathelicidin. Further work will clarify the boundaries of the norm and explore various cases of impaired immunity.
dc.language.isoeng
dc.titleMultigene expression assay for assessment of the immune status of Atlantic Salmon
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber1-11
dc.source.volume11
dc.source.journalGenes
dc.source.issue11
dc.identifier.doi10.3390/genes11111236
dc.identifier.cristin1847153
dc.relation.projectNorges forskningsråd: 267644
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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