Park Sun Young, Lee Sim-In, Jin Jong Sook, Kim Eun-Sol, Kim Jae Young, Kim Ah-Young, Park Sang Hyun, Park Jung-Won, Park Soonyong, Lee Eun Gyo, Park Jong-Hyeon, Ko Young-Joon, Park Choi-Kyu
Center for FMD Vaccine Research, Animal and Plant Quarantine Agency, 177 Hyeoksin-8-ro, Gimcheon-si 39660, Korea.
Animal Disease Intervention Center, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
Vaccines (Basel). 2022 Jun 24;10(7):1018. doi: 10.3390/vaccines10071018.
Foot-and-mouth disease (FMD) is an economically important and highly infectious viral disease, predominantly controlled by vaccination. The removal of non-structural proteins (NSPs) is very important in the process of FMD vaccine production, because vaccinated and naturally infected animals can be distinguished by the presence of NSP antibodies in the FMD serological surveillance. A previous study reported that 3AB protein, a representative of NSPs, was removed by chloroform treatment. Therefore, in this study, the causes of 3AB removal and factors affecting the effect of chloroform were investigated. As a result, the effectiveness of chloroform differed depending on the virus production medium and was eliminated by detergents. In addition, it was found that 3AB protein removal by chloroform is due to the transmembrane domain of the N-terminal region (59-76 amino acid domain). Further, industrial applicability was verified by applying the chloroform treatment process to scale-up FMD vaccine antigen production. A novel downstream process using ultrafiltration instead of polyethylene glycol precipitation for high-purity FMD vaccine antigen production was established. This result will contribute toward simplifying the conventional process of manufacturing FMD vaccine antigens and ultimately reducing the time and cost of vaccine production.
口蹄疫(FMD)是一种具有重要经济意义的高度传染性病毒病,主要通过疫苗接种进行防控。在口蹄疫疫苗生产过程中,去除非结构蛋白(NSPs)非常重要,因为在口蹄疫血清学监测中,可通过NSP抗体的存在来区分接种疫苗的动物和自然感染的动物。先前的一项研究报道,NSPs的代表3AB蛋白可通过氯仿处理去除。因此,在本研究中,对3AB去除的原因及影响氯仿效果的因素进行了研究。结果表明,氯仿的有效性因病毒生产培养基而异,并可被去污剂消除。此外,发现氯仿去除3AB蛋白是由于N端区域的跨膜结构域(59 - 76氨基酸结构域)。此外,通过将氯仿处理工艺应用于口蹄疫疫苗抗原的规模化生产,验证了其工业适用性。建立了一种使用超滤代替聚乙二醇沉淀的新型下游工艺,用于生产高纯度口蹄疫疫苗抗原。这一结果将有助于简化口蹄疫疫苗抗原的传统生产工艺,并最终降低疫苗生产的时间和成本。