Production of a Bacteria-like Particle Vaccine Targeting Rock Bream (Oplegnathus fasciatus) Iridovirus Using Nicotiana benthamiana.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2022-01-01 Epub Date: 2021-09-28 DOI:10.1007/s12374-021-09328-z
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
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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.

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利用本菌烟制备针对石鲷虹膜病毒的细菌样颗粒疫苗。
病毒性疾病是一种极其广泛的传染病,通过突变不断发生变化。为了生产针对病毒性疾病的疫苗,瞬态表达系统被采用,而烟(烟草)植物是一个迅速扩展的平台。本研究以虹膜病毒的主要衣壳蛋白(MCP)为靶点,与赖氨酸基序(LysM)和冠状蛋白1的卷曲结构域(ccCor1)融合,利用乳酸乳球菌进行表面展示。该蛋白在n -糖基化形式的benthamiana中大量产生。通过增加硫酸铵溶液的浓度,对侵染的红叶总可溶性蛋白进行顺序处理,重组MCP主要沉淀在40 ~ 60%。采用Ni-NTA树脂亲和层析进一步纯化。用粒径不相容色谱法进行天然结构分析表明,重组MCP以大的低聚形式存在。在三氯乙酸(TCA)处理的乳酸菌中,OD600值至少为0.4才能有效地显示重组MCP。采用酶联免疫吸附法(ELISA)评价重组MCP在小鼠模型中的免疫原性。综上所述,我们开发了一种结合乳杆菌表面展示的植物重组疫苗生产体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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