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Cited 6 time in webofscience Cited 6 time in scopus
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Production of a Bacteria-like Particle Vaccine Targeting Rock Bream (Oplegnathus fasciatus) Iridovirus Using Nicotiana benthamiana

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dc.contributor.authorAhn, Gyeongik-
dc.contributor.authorCha, Joon-Yung-
dc.contributor.authorLee, Jeong Won-
dc.contributor.authorPark, Gyeongran-
dc.contributor.authorShin, Gyeong-Im-
dc.contributor.authorSong, Shi-Jian-
dc.contributor.authorRyu, Gyeongryul-
dc.contributor.authorHwang, Inhwan-
dc.contributor.authorKim, Min Gab-
dc.contributor.authorKim, Woe-Yeon-
dc.date.accessioned2022-12-26T07:21:29Z-
dc.date.available2022-12-26T07:21:29Z-
dc.date.issued2022-02-
dc.identifier.issn1226-9239-
dc.identifier.issn1867-0725-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/1650-
dc.description.abstractViral diseases are extremely widespread infections that change constantly through mutations. To produce vaccines against viral diseases, transient expression systems are employed, and Nicotiana benthamiana (tobacco) plants are a rapidly expanding platform. In this study, we developed a recombinant protein vaccine targeting the major capsid protein (MCP) of iridovirus fused with the lysine motif (LysM) and coiled-coil domain of coronin 1 (ccCor1) for surface display using Lactococcus lactis. The protein was abundantly produced in N. benthamiana in its N-glycosylated form. Total soluble proteins isolated from infiltrated N. benthamiana leaves were treated sequentially with increasing ammonium sulfate solution, and recombinant MCP mainly precipitated at 40-60%. Additionally, affinity chromatography using Ni-NTA resin was applied for further purification. Native structure analysis using size exclusion chromatography showed that recombinant MCP existed in a large oligomeric form. A minimum OD600 value of 0.4 trichloroacetic acid (TCA)-treated L. lactis was required for efficient recombinant MCP display. Immunogenicity of recombinant MCP was assessed in a mouse model through enzyme-linked immunosorbent assay (ELISA) with serum-injected recombinant MCP-displaying L. lactis. In summary, we developed a plant-based recombinant vaccine production system combined with surface display on L. lactis.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisher한국식물학회-
dc.titleProduction of a Bacteria-like Particle Vaccine Targeting Rock Bream (Oplegnathus fasciatus) Iridovirus Using Nicotiana benthamiana-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/s12374-021-09328-z-
dc.identifier.scopusid2-s2.0-85115849034-
dc.identifier.wosid000701797400001-
dc.identifier.bibliographicCitationJournal of Plant Biology, v.65, no.1, pp 21 - 28-
dc.citation.titleJournal of Plant Biology-
dc.citation.volume65-
dc.citation.number1-
dc.citation.startPage21-
dc.citation.endPage28-
dc.type.docTypeArticle-
dc.identifier.kciidART002809060-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.subject.keywordPlusRED-SEA BREAM-
dc.subject.keywordPlusMAJOR CAPSID PROTEIN-
dc.subject.keywordPlusGROUPER IRIDOVIRUS-
dc.subject.keywordPlusINFECTIOUS SPLEEN-
dc.subject.keywordPlusCULTURED FISH-
dc.subject.keywordPlusPAGRUS-MAJOR-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusTEMMINCK-
dc.subject.keywordPlusMOTIF-
dc.subject.keywordAuthorBacteria-like particle-
dc.subject.keywordAuthorIridovirus-
dc.subject.keywordAuthorMajor capsid protein-
dc.subject.keywordAuthorNicotiana benthamiana-
dc.subject.keywordAuthorPlant-based vaccine-
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