Publication:
Detections of Rainbow Trout Antibodies to Infectious Pancreatic Necrosis Virus and Viral Hemorrhagic Septicemia Virus via a Recombinant Protein-Based Enzyme-Linked Immunosorbent Assay

dc.authorscopusid57189622256
dc.authorscopusid15022421000
dc.authorscopusid15022065800
dc.contributor.authorTamer, C.
dc.contributor.authorGümüşova, S.
dc.contributor.authorAlbayrak, H.
dc.date.accessioned2025-12-11T00:29:34Z
dc.date.issued2022
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Tamer] Cüneyt, Department of Virology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Gümüşova] Semra Okur, Department of Virology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Albayrak] Harun, Department of Virology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractInfectious Pancreatic Necrosis Virus (IPNV) and Viral hemorrhagic septicemia virus (VHSV) cause significant losses in the aquaculture industry. There have been few reports of the use of screening rainbow trout for antibodies against IPNV and VHSV as an epidemiological tool. Several ELISAs using a whole virus or recombinant IPNV and VHSV proteins have been described. In this study, a recombinant protein-based enzyme-linked immunosorbent assay (ELISA) for the detection of IPNV and VHSV antibodies in rainbow trout (Oncorhynchus mykiss) was evaluated. To develop recombinant protein-based enzyme-linked immunosorbent assays, a fragment containing the entire length of the gG gene of VHSV and VP2 of IPNV was amplified by PCR using the viruses' genomic RNA and cloned in pET-28a(+) plasmid. Recombinant structural viral proteins (rVP2 and rgG) were expressed in the Escherichia coli BL21 (DE3). The rgG was extracted and purified. 96-well plates were coated with VP2 and gG separately. For VHSV, Assay could detect until 1/15625 dilution in VHSV positive fish serum. For IPNV, Assays could detect until 1/3125 dilution in IPNV positive fish serum. These results show rgG and rVP2, used in ELISA, are more sensitive than virus neutralization tests. et al., 2018). IPNV is a member of the Aquabirnavirus. © 2022, Central Fisheries Research Inst. All rights reserved.en_US
dc.identifier.doi10.4194/AQUAST669
dc.identifier.issn2618-6381
dc.identifier.issn2651-3668
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-85116408979
dc.identifier.scopusqualityQ3
dc.identifier.urihttps://doi.org/10.4194/AQUAST669
dc.identifier.urihttps://hdl.handle.net/20.500.12712/36757
dc.identifier.volume22en_US
dc.language.isoenen_US
dc.publisherCentral Fisheries Research Instituteen_US
dc.relation.ispartofAquaculture Studiesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectELISAen_US
dc.subjectIPNVen_US
dc.subjectRecombinant Proteinen_US
dc.subjectVHSVen_US
dc.titleDetections of Rainbow Trout Antibodies to Infectious Pancreatic Necrosis Virus and Viral Hemorrhagic Septicemia Virus via a Recombinant Protein-Based Enzyme-Linked Immunosorbent Assayen_US
dc.typeArticleen_US
dspace.entity.typePublication

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