Soluble expression and immunogenicity analysis of capsid proteins of porcine circoviruses types 2, 3, and 4

猪圆环病毒 免疫原性 衣壳 重组DNA 生物素化 病毒学 佐剂 生物 分子生物学 融合蛋白 体液免疫 圆环病毒 免疫系统 免疫学 病毒 抗体 生物化学 基因
作者
Huimin Zhang,Xue Li,Xinru Lv,Yaqi Han,Jiawei Zheng,Linzhu Ren
出处
期刊:Veterinary Journal [Elsevier BV]
卷期号:307: 106199-106199 被引量:4
标识
DOI:10.1016/j.tvjl.2024.106199
摘要

Porcine circoviruses (PCVs) contain four types: PCV1, PCV2, PCV3, and PCV4, all of which can infect pigs. Among them, PCV1 is non-pathogenic, and PCV2 can cause porcine circovirus diseases (PCVD) or porcine circovirus-associated diseases (PCVAD). Although the pathogenicity of PCV3 and PCV4 is still controversial, increasing evidence shows that PCV3 and PCV4 can cause PCV-related disease. However, mixed infection of PCV2, PCV3, and PCV4 with other pathogens often occurs in large-scale pig breeding, bringing severe economic losses to the global pig industry. In this study, the soluble recombinant proteins of PCV2, PCV3, and PCV4 Cap were expressed by the prokaryotic expression system and biotinylated to combine with the Streptavidin magnetic beads, followed by immunogenicity evaluation of the recombinant proteins. Furthermore, we also assessed the efficacy and immunogenicity of trivalent recombinant proteins conjugated with different adjuvants in mice. The results showed that the highly effective anti-PCV serum was successfully prepared, and the recombinant proteins conjugated with different adjuvants produced various degrees of humoral and cellular immunity in mice. Three recombinant proteins are effective immunogens, and the trivalent proteins coupled with the aluminum adjuvant or GM-CSF-CpG for two-dose immunization can stimulate prominent humoral and cellular immunity against PCVs in vivo. The soluble recombinant proteins are the most promising candidate for developing a trivalent vaccine against PCVs (PCV2, PCV3, and PCV4) infection simultaneously.
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