Gyeongik Ahn, Joon-Yung Cha, Jeong Won Lee, Gyeongran Park, Gyeong-Im Shin, Shi-Jian Song, Gyeongryul Ryu, Inhwan Hwang, Min Gab Kim, Woe-Yeon Kim
{"title":"Production of a Bacteria-like Particle Vaccine Targeting Rock Bream (<i>Oplegnathus fasciatus</i>) Iridovirus Using <i>Nicotiana benthamiana</i>.","authors":"Gyeongik Ahn, Joon-Yung Cha, Jeong Won Lee, Gyeongran Park, Gyeong-Im Shin, Shi-Jian Song, Gyeongryul Ryu, Inhwan Hwang, Min Gab Kim, Woe-Yeon Kim","doi":"10.1007/s12374-021-09328-z","DOIUrl":null,"url":null,"abstract":"<p><p>Viral diseases are extremely widespread infections that change constantly through mutations. To produce vaccines against viral diseases, transient expression systems are employed, and <i>Nicotiana benthamiana</i> (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 <i>Lactococcus lactis</i>. The protein was abundantly produced in <i>N. benthamiana</i> in its <i>N</i>-glycosylated form. Total soluble proteins isolated from infiltrated <i>N. benthamiana</i> 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 OD<sub>600</sub> value of 0.4 trichloroacetic acid (TCA)-treated <i>L. lactis</i> 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 <i>L. lactis</i>. In summary, we developed a plant-based recombinant vaccine production system combined with surface display on <i>L. lactis</i>.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477727/pdf/","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s12374-021-09328-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/9/28 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 1
Abstract
Viral 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.