Microcrystalline cellulose for delivery of recombinant protein-based antigen against erysipelas in mice

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dc.contributor.authorWooyoung Jeon-
dc.contributor.authorY C Kim-
dc.contributor.authorMinhee Hong-
dc.contributor.authorR Rejinold-
dc.contributor.authorK Park-
dc.contributor.authorI Yoon-
dc.contributor.authorS Yoo-
dc.contributor.authorHong-Weon Lee-
dc.contributor.authorJungoh Ahn-
dc.date.accessioned2018-10-24T16:30:07Z-
dc.date.available2018-10-24T16:30:07Z-
dc.date.issued2018-
dc.identifier.issn2314-6133-
dc.identifier.uri10.1155/2018/7670505ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17983-
dc.description.abstractThe study describes the development of a vaccine using microcrystalline cellulose (Avicel PH-101) as a delivery carrier of recombinant protein-based antigen against erysipelas. Recombinant SpaA, surface protective protein, from a gram-positive pathogen Erysipelothrix rhusiopathiae was fused to a cellulose-binding domain (CBD) from Trichoderma harzianum endoglucanase II through a S3N10 peptide. The fusion protein (CBD-SpaA) was expressed in Escherichia coli and was subsequently bound to Avicel PH-101. The antigenicity of CBD-SpaA bound to the Avicel was evaluated by enzyme-linked immunosorbent (ELISA) and confocal laser scanning microscope (CLSM) assays. For the examination of its immunogenicity, groups of mice were immunized with different constructs (soluble CBD-SpaA, Avicel coated with CBD-SpaA, whole bacterin of E. rhusiopathiae (positive control), and PBS (negative control)). In two weeks after immunization, mice were challenged with 1x107 CFU of E. rhusiopathiae and Avicel coated with CBD-SpaA induced protective immunity in mice. In conclusion, this study demonstrates the feasibility of microcrystalline cellulose as the delivery system of recombinant protein subunit vaccine against E. rhusiopathiae infection in mice.-
dc.publisherHindawi Ltd-
dc.titleMicrocrystalline cellulose for delivery of recombinant protein-based antigen against erysipelas in mice-
dc.title.alternativeMicrocrystalline cellulose for delivery of recombinant protein-based antigen against erysipelas in mice-
dc.typeArticle-
dc.citation.titleBiomed Research International-
dc.citation.number0-
dc.citation.endPage7670505-
dc.citation.startPage7670505-
dc.citation.volume2018-
dc.contributor.affiliatedAuthorWooyoung Jeon-
dc.contributor.affiliatedAuthorMinhee Hong-
dc.contributor.affiliatedAuthorHong-Weon Lee-
dc.contributor.affiliatedAuthorJungoh Ahn-
dc.contributor.alternativeName전우영-
dc.contributor.alternativeName김예춘-
dc.contributor.alternativeName홍민희-
dc.contributor.alternativeNameRejinold-
dc.contributor.alternativeName박경문-
dc.contributor.alternativeName윤인중-
dc.contributor.alternativeName유성식-
dc.contributor.alternativeName이홍원-
dc.contributor.alternativeName안정오-
dc.identifier.bibliographicCitationBiomed Research International, vol. 2018, pp. 7670505-7670505-
dc.identifier.doi10.1155/2018/7670505-
dc.description.journalClassY-
Appears in Collections:
Division of Bio Technology Innovation > BioProcess Engineering Center > 1. Journal Articles
Division of Bio Technology Innovation > 1. Journal Articles
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