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":"利用本菌烟制备针对石鲷虹膜病毒的细菌样颗粒疫苗。","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":"{\"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}","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}
Production of a Bacteria-like Particle Vaccine Targeting Rock Bream (Oplegnathus fasciatus) Iridovirus Using Nicotiana benthamiana.
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.