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Trigger factor assisted self-assembly of canine parvovirus VP2 protein into virus-like particles in Escherichia coli with high immunogenicity

机译:触发因子辅助在大肠杆菌中的病毒样颗粒的自我组装成具有高免疫原性的病毒样颗粒

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摘要

Abstract Canine parvovirus (CPV) has been considered to be an important pathogen, which can cause acute infectious disease in canids. Although current vaccines are effective in preventing CPV infection, safety problems still remain unsolved. In this study, a subunit vaccine against CPV based on virus-like particles (VLPs) with good safety and immunogenicity is reported. Soluble CPV VP2 protein was produced by co-expression of chaperone trigger factor (Tf16) in Escherichia coli (E.coli), and assembled into CPV VLPs which could be affected by NaCl and pH. At 250 mM NaCl pH 8.0, the VLPs co-expressed with Tf16 had similar size (25 nm) and shape with the authentic virus capsid under the transmission electron microscopy (TEM), which is also in accordance with the dynamic light scattering (DLS) data. Immunization with these particles could induce high-titer hemagglutination inhibition (1:12288) and neutralizing antibodies (1:6144) in guinea pigs. Splenic cells of them could secrete IFN-γ and IL-4 after stimulation by CPV. Thus, the VLPs produced by the new approach with high yield and immunogenicity could be a potential candidate for CPV vaccine.
机译:摘要犬宫瓣病毒(CPV)被认为是一个重要的病原体,这可能导致CANID中的急性传染病。虽然目前的疫苗有效地防止CPV感染,但安全问题仍然仍未解决。在该研究中,报道了基于病毒样颗粒(VLP)的亚次亚基疫苗具有良好的安全性和免疫原性。通过在大肠杆菌(大肠杆菌)中的伴侣触发因子(TF16)的共表达,并组装成可受到NaCl和pH的影响的CPV VLP产生的可溶性CPV VP2蛋白。在250mM NaCl pH 8.0中,用TF16共表达的VLP具有相似的尺寸(25nm),并且在透射电子显微镜(TEM)下具有正宗的病毒衣壳的形状,这也根据动态光散射(DLS)。数据。用这些颗粒免疫可以诱导高滴血血凝抑制(1:12288)和豚鼠中的中和抗体(1:6144)。通过CPV刺激后,它们的脾细胞可以分泌IFN-γ和IL-4。因此,通过高产率和免疫原性产生的新方法产生的VLP可以是CPV疫苗的潜在候选者。

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