Choi Hwi-Yeon, Kim Min-Sik, Kang Yeong-Lim, Choi Jong-Chul, Choi In-Yeong, Jung Sung-Won, Jeong Ji-Yun, Kim Min-Chul, Hwang Seong-Soo, Lee Sang-Won, Park Seung-Yong, Song Chang-Seon, Choi In-Soo, Lee Joong-Bok
Laboratory of Infectious Diseases, College of Veterinary Medicine, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Korea.
Careside Co. Ltd., Woolim Lions Valley A-B210, #146-8, Sangdaewon-dong, Jungwon-gu, Seongnam 13209, Gyeonggi-do, Korea.
Vet Sci. 2022 Mar 29;9(4):165. doi: 10.3390/vetsci9040165.
Vaccination is a practical method to provide protection against porcine reproductive and respiratory syndrome virus (PRRSV), but current PRRSV vaccines show limited efficacy against divergent field strains. Lineage 1 PRRSV includes virulent strains such as NADC30 and MN184 and now has become one of the most prevalent viruses in Korea. Accordingly, there is an urgent need to develop a new vaccine for Korean lineage-1 strains. In this study, a vaccine candidate against Korean lineage-1 PRRSV, vCSL1-GP5-N33D, was developed by reverse genetics technology. vCSL1-GP5-N33D was designed as a hypo-glycosylated chimeric virus containing the glycoprotein 5 ectodomain region of the Korean lineage-1 wild-type strain. An inactivated vaccine of vCSL1-GP5-N33D was applied to a PRRS-endemic farm and elicited high serum virus neutralization (SVN) antibody titers. The vaccinated group induced SVN antibody titers of 4.40 (log) ± 2.46, which were approximately 2-fold higher than those of the negative control at 8-weeks post-vaccination. Moreover, 60% of pigs in the vaccinated group displayed SVN antibody titers of ≥5 (log), while none of the pigs in the negative control exhibited SVN antibody titers of ≥5 (log). The overall results of the animal experiment suggest that the vCSL1-GP5-N33D inactivated vaccine is a promising vaccine candidate.
接种疫苗是预防猪繁殖与呼吸综合征病毒(PRRSV)的一种实用方法,但目前的PRRSV疫苗对不同的田间毒株显示出有限的效力。1型PRRSV包括NADC30和MN184等强毒株,现已成为韩国最流行的病毒之一。因此,迫切需要开发一种针对韩国1型毒株的新型疫苗。在本研究中,通过反向遗传学技术开发了一种针对韩国1型PRRSV的候选疫苗vCSL1-GP5-N33D。vCSL1-GP5-N33D被设计为一种低糖基化嵌合病毒,包含韩国1型野生型毒株的糖蛋白5胞外域区域。vCSL1-GP5-N33D的灭活疫苗应用于一个PRRS地方病猪场,并引发了高血清病毒中和(SVN)抗体滴度。接种疫苗的组在接种后8周诱导的SVN抗体滴度为4.40(log)±2.46,比阴性对照组高约2倍。此外,接种疫苗组60%的猪显示SVN抗体滴度≥5(log),而阴性对照组没有猪的SVN抗体滴度≥5(log)。动物实验的总体结果表明,vCSL1-GP5-N33D灭活疫苗是一种有前景的候选疫苗。