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dc.contributor.authorGislefoss, Elisabeth
dc.contributor.authorGamil, Amr Ahmed Abdelrahim
dc.contributor.authorØvergård, Aina-Cathrine
dc.contributor.authorEvensen, Øystein
dc.date.accessioned2024-01-17T13:37:18Z
dc.date.available2024-01-17T13:37:18Z
dc.date.created2023-10-30T14:53:38Z
dc.date.issued2023
dc.identifier.issn2589-0042
dc.identifier.urihttps://hdl.handle.net/11250/3112224
dc.description.abstractSalmon louse, Lepeophtheirus salmonis, represents major challenge for salmon farming. Current treatments impose welfare issues and are costly, whereas prophylactic measures are unavailable. Two salmon louse heme peroxidases (LsPxtl-1 and LsPxtl-2) were tested for their importance for parasite development and as potential vaccine candidates. LsPxtl-1 possesses two heme peroxidase domains and is expressed in ovaries and gut, whereas LsPxtl-2 encodes one domain and contains N-terminal signal peptide and an Eph receptor ligand-binding domain. LsPxtl-1, but not LsPxtl-2, knockdown in nauplius II stage caused poor swimming and death, indicating its importance for parasite development. Immunizations using single DNA plasmid injection encoding the peroxidases or heterologous prime (DNA) and boost (recombinant LsPxtl-2 protein) gave non-significant reduction in lice numbers. Single injection gave low specific antibody levels compared with the prime-boost. The findings suggest LsPxtl-1 is important for parasite development but formulations and vaccination modalities used did not significantly reduce lice infestation.en_US
dc.language.isoengen_US
dc.publisherCell Pressen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleIdentification and characterization of two salmon louse heme peroxidases and their potential as vaccine antigensen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.source.articlenumber107991en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1016/j.isci.2023.107991
dc.identifier.cristin2190109
dc.source.journaliScienceen_US
dc.identifier.citationiScience. 2023, 26 (10), 107991.en_US
dc.source.volume26en_US
dc.source.issue10en_US


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