Yu Fulai, Xiang Wei, Ou Weiye, Li Yang, Shu Xinbiao, Li Xiaoliang
Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.
Zhejiang Dovro Animal Health Products Co., Ltd., 298 Binhong West Road, Jinhua 321017, China.
Vet Sci. 2025 Jan 7;12(1):25. doi: 10.3390/vetsci12010025.
Diseases associated with porcine circovirus type 2 (PCV2) and pseudorabies virus (PRV) significantly affect the economy of pig farms, particularly when combined infections lead to bacterial co-infections. Antigens from the pseudorabies variant strain gB and gD proteins and PCV2 (genotyped) Cap protein were mixed with the pattern recognition receptor (PRR) agonist FLICd as adjuvants and formulated with a micro-hydrogel adjuvant into PCV2 and PRV bivalent subunit vaccines. Twenty pigs, aged 30-35 days, were divided into groups A (received bivalent subunit vaccine) and B (received bivalent subunit vaccines with recombinant FLICd adjuvant), as well as C (non-vaccinated challenge control) and D (blank control). Groups A and B showed no significant difference in average daily weight gain compared to the unvaccinated controls. Fourteen days post-second vaccination, groups A and B exhibited significantly higher levels of PRV and PCV2 antibodies than groups C and D. Group B showed significantly higher average titers of PRV-specific neutralizing antibodies than group A. Fourteen days post-second vaccination, a PRV (ZJM-1 strain) challenge test was conducted. The vaccinated group achieved 100% protection. Vaccination effectively reduced virus load post-challenge and shortened the PRV shedding period. Vaccination with PCV2 and PRV bivalent subunit vaccines effectively prevents the onset of PCV2-related diseases and infections by wild pseudorabies strains.
与猪圆环病毒2型(PCV2)和伪狂犬病病毒(PRV)相关的疾病严重影响养猪场的经济,尤其是当混合感染导致细菌合并感染时。将伪狂犬病变异株gB和gD蛋白以及PCV2(基因分型)Cap蛋白的抗原与模式识别受体(PRR)激动剂FLICd作为佐剂混合,并与微水凝胶佐剂一起制成PCV2和PRV二价亚单位疫苗。将20头30 - 35日龄的猪分为A组(接受二价亚单位疫苗)、B组(接受含重组FLICd佐剂的二价亚单位疫苗),以及C组(未接种疫苗的攻毒对照组)和D组(空白对照组)。与未接种疫苗的对照组相比,A组和B组的平均日增重无显著差异。第二次接种疫苗14天后,A组和B组的PRV和PCV2抗体水平显著高于C组和D组。B组的PRV特异性中和抗体平均滴度显著高于A组。第二次接种疫苗14天后,进行了PRV(ZJM - 1株)攻毒试验。接种疫苗组实现了100%的保护。接种疫苗有效降低了攻毒后的病毒载量,并缩短了PRV排毒期。接种PCV2和PRV二价亚单位疫苗可有效预防PCV2相关疾病的发生以及野生伪狂犬病病毒株的感染。