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Enhancement of glycoprotein-based DNA vaccine for viral hemorrhagic septicemia virus (VHSV) via addition of the molecular adjuvant, DDX41

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dc.contributor.authorLazarte, Jassy Mary S.-
dc.contributor.authorKim, Young Rim-
dc.contributor.authorLee, Jung Seok-
dc.contributor.authorIm, Se Pyeong-
dc.contributor.authorKim, Si Won-
dc.contributor.authorJung, Jae Wook-
dc.contributor.authorKim, Jaesung-
dc.contributor.authorLee, Woo Jai-
dc.contributor.authorJung, Tae Sung-
dc.date.accessioned2022-12-26T18:49:35Z-
dc.date.available2022-12-26T18:49:35Z-
dc.date.issued2017-03-
dc.identifier.issn1050-4648-
dc.identifier.issn1095-9947-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13867-
dc.description.abstractThe use of molecular adjuvants to improve the immunogenicity of DNA vaccines has been thoroughly studied in recent years. Glycoprotein (G)-based DNA vaccines had been proven to be effective in combating infection against Rhabdovirus (especially infectious hematopoietic necrosis virus, IHNV) in salmonids. DDX41 is a helicase known to induce antiviral and inflammatory responses by inducing a type I IFN innate immune response. To gain more information regarding G-based DNA vaccines in olive flounder (Paralicthys olivaceus), we tried to develop a more efficient G-based DNA vaccine by adding a molecular adjuvant, DDX41. We designed a DNA vaccine in which the VHSV glycoprotein (G-protein) and DDX41 were driven by the EF-1 alpha and CMV promoters, respectively. Olive flounders were intramuscularly immunized with 1 mu g of plasmids encoding the G-based DNA vaccine alone (pEF-G), the molecular adjuvant alone (pEF-D), or the vaccine-adjuvant construct (pEF-GD). At two different time points, 15 and 30 days later, the fish were intraperitoneally infected with VHSV (100 mu L; 1 x 10(6) TCID50/mL). Our assays revealed that the plasmid constructs showed up-regulated expression of IFN-1 and its associated genes at day 3 post-vaccination in both kidney and spleen samples. Specifically, pEF-GD showed statistically higher expression of immune response genes than pEF-G and pEF-D treated group (p < 0.05/p < 0.001). After VHSV challenge, the fish group treated with pEF-GD showed higher survival rate than the pEF-G treated group, though difference was not statistically significant in the 15 dpv challenged group however in the 30 dpv challenged group, the difference was statistically significant (p < 0.05). Together, these results clearly demonstrate that DDX41 is an effective adjuvant for the G-based DNA vaccine in olive flounder. Our novel findings could facilitate the development of more effective DNA vaccines for the aquaculture industry. (C) 2017 Elsevier Ltd. All rights reserved.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titleEnhancement of glycoprotein-based DNA vaccine for viral hemorrhagic septicemia virus (VHSV) via addition of the molecular adjuvant, DDX41-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.fsi.2017.01.031-
dc.identifier.scopusid2-s2.0-85012107878-
dc.identifier.wosid000395955800039-
dc.identifier.bibliographicCitationFish and Shellfish Immunology, v.62, pp 356 - 365-
dc.citation.titleFish and Shellfish Immunology-
dc.citation.volume62-
dc.citation.startPage356-
dc.citation.endPage365-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaFisheries-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaMarine & Freshwater Biology-
dc.relation.journalResearchAreaVeterinary Sciences-
dc.relation.journalWebOfScienceCategoryFisheries-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryMarine & Freshwater Biology-
dc.relation.journalWebOfScienceCategoryVeterinary Sciences-
dc.subject.keywordPlusHEMATOPOIETIC NECROSIS VIRUS-
dc.subject.keywordPlusPARALICHTHYS-OLIVACEUS-
dc.subject.keywordPlusJAPANESE FLOUNDER-
dc.subject.keywordPlusRAINBOW-TROUT-
dc.subject.keywordPlusPROTECTIVE IMMUNITY-
dc.subject.keywordPlusHIRAME RHABDOVIRUS-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusCYPRINUS-CARPIO-
dc.subject.keywordPlusI INTERFERON-
dc.subject.keywordPlusRIG-I-
dc.subject.keywordAuthorDDX41-
dc.subject.keywordAuthorGlycoprotein-
dc.subject.keywordAuthorVHSV-
dc.subject.keywordAuthorInterferon-
dc.subject.keywordAuthorInnate immune system-
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