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Virus-Like Particles of Chimeric Recombinant Porcine Circovirus Type 2 as Antigen Vehicle Carrying Foreign Epitopes

机译:嵌合重组猪圆环病毒2型病毒样颗粒作为携带外源抗原决定簇的抗原载体

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摘要

Virus-like particles (VLPs) of chimeric porcine circovirus type 2 (PCV2) were generated by replacing the nuclear localization signal (NLS; at 1–39 aa) of PCV2 capsid protein (Cap) with classical swine fever virus (CSFV) T-cell epitope (1446–1460 aa), CSFV B-cell epitope (693–716 aa) and CSFV T-cell epitope conjugated with B-cell epitope. The recombinant proteins were expressed using the baculovirus expression system and detected by immunoblotting and indirect immunofluorescence assay. The abilities to form PCV2 VLPs were confirmed by transmission electron microscopy. Immunogenicities of the three recombinant proteins were evaluated in mice. Our Results indicated that Cap protein NLS deletion or substitution with CSFV epitopes did not affect the VLPs assembly. Three chimeric Cap proteins could form VLPs and induce efficient humoral and cellular immunity against PCV2 and CSFV in mice. Results show that PCV2 VLPs can be used as an efficient antigen carrier for delivery of foreign epitopes, and a potential novel vaccine.
机译:嵌合猪圆环病毒2型(PCV2)的病毒样颗粒(VLP)是用经典猪瘟病毒(CSFV)T-取代PCV2衣壳蛋白(Cap)的核定位信号(NLS;在1–39aa)细胞表位(1446–1460 aa),CSFV B细胞表位(693–716 aa)和与B细胞表位结合的CSFV T细胞表位。使用杆状病毒表达系统表达重组蛋白,并通过免疫印迹和间接免疫荧光测定进行检测。通过透射电子显微镜确认了形成PCV2 VLP的能力。在小鼠中评估了三种重组蛋白的免疫原性。我们的结果表明Cap蛋白NLS缺失或被CSFV表位取代不会影响VLP装配。三种嵌合Cap蛋白可以形成VLP,并在小鼠中诱导针对PCV2和CSFV的有效体液和细胞免疫。结果表明,PCV2 VLP可用作有效的抗原载体,用于运送外源抗原决定簇和潜在的新型疫苗。

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