Animal Virology Laboratory, School of Life Sciences, BK21 plus KNU Creative BioResearch Group, Kyungpook National University, Daegu, 41566, Republic of Korea.
ChoongAng Vaccine Laboratories, Daejeon, 34055, Republic of Korea; Department of Infectious Diseases, College of Veterinary Medicine, Seoul National University, Seoul, 08826, Republic of Korea.
Vet Microbiol. 2019 Apr;231:120-128. doi: 10.1016/j.vetmic.2019.03.009. Epub 2019 Mar 11.
We have previously reported the generation of the attenuated KNU-141112-S DEL5/ORF3 virus by continuous propagation of highly virulent G2b porcine epidemic diarrhea virus (PEDV) in Vero cells. The present study aimed to assess the safety of S DEL5/ORF3 and to evaluate its effectiveness as a live vaccine for prime-booster vaccinations. Reversion to virulence experiments revealed that the S DEL5/ORF3 strain retains its attenuated phenotype and genetic stability after five successive passages in susceptible piglets. Pregnant sows were primed orally with an S DEL5/ORF3 live vaccine and boosted intramuscularly twice with a commercial killed vaccine at 2-week intervals prior to parturition. This sow vaccination regimen completely protected nursing piglets against virulent G2b challenge, as evidenced by the increase in survival rate from 0% to 100% and the significant reduction in diarrhea intensity, including the amount and duration of PEDV fecal shedding. In addition, despite a 2-3 day period of weight loss in piglets from vaccinated sows after challenge, their daily weight gain was recovered at 7 days post-challenge and became similar to that of unchallenged pigs from unvaccinated sows over the course of the experiment. Furthermore, strong antibody responses to PEDV were verified in the sera and colostrum of immunized sows with the prime-boost treatment and their offspring. Altogether, our data demonstrated that the attenuated S DEL5/ORF3 strain guarantees the safety to host animals with no reversion to virulence and is suitable as an effective primary live vaccine providing durable maternal lactogenic immunity for passive piglet protection.
我们之前报道了通过在 Vero 细胞中连续传代高致病性 G2b 猪流行性腹泻病毒(PEDV)来产生减毒 KNU-141112-S DEL5/ORF3 病毒。本研究旨在评估 S DEL5/ORF3 的安全性,并评估其作为活疫苗进行初次-加强免疫接种的效果。回复毒性实验表明,S DEL5/ORF3 株在易感仔猪中连续传代 5 次后仍保持其减毒表型和遗传稳定性。怀孕母猪经口接种 S DEL5/ORF3 活疫苗进行初次免疫,分娩前 2 周间隔肌肉注射两次商业灭活疫苗进行加强免疫。这种母猪免疫接种方案完全保护哺乳仔猪免受强毒 G2b 挑战,从存活率从 0%增加到 100%和腹泻严重程度的显著降低(包括 PEDV 粪便脱落量和持续时间)得到证明。此外,尽管接种母猪的仔猪在挑战后会出现 2-3 天的体重减轻,但在挑战后 7 天,它们的日增重恢复正常,并且在整个实验过程中与未接种母猪的未挑战仔猪相似。此外,初次-加强免疫接种母猪及其后代的血清和初乳中均证实对 PEDV 产生了强烈的抗体反应。总之,我们的数据表明,减毒 S DEL5/ORF3 株保证了宿主动物的安全性,没有回复毒性的风险,并且适合作为一种有效的初级活疫苗,为被动仔猪保护提供持久的母源乳源性免疫力。