Swanson Jessica, Fragkoudis Rennos, Hawes Philippa C, Newman Joseph, Burman Alison, Panjwani Anusha, Stonehouse Nicola J, Tuthill Tobias J
The Pirbright Institute, Pirbright GU24 0NF, UK.
Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
Life (Basel). 2021 Apr 11;11(4):338. doi: 10.3390/life11040338.
The picornavirus foot-and-mouth disease virus (FMDV) is the causative agent of the economically important disease of livestock, foot-and-mouth disease (FMD). VP4 is a highly conserved capsid protein, which is important during virus entry. Previous published work has shown that antibodies targeting the N-terminus of VP4 of the picornavirus human rhinovirus are broadly neutralising. In addition, previous studies showed that immunisation with the N-terminal 20 amino acids of enterovirus A71 VP4 displayed on the hepatitis B core (HBc) virus-like particles (VLP) can induce cross-genotype neutralisation. To investigate if a similar neutralising response against FMDV VP4 could be generated, HBc VLPs displaying the N-terminus of FMDV VP4 were designed. The N-terminal 15 amino acids of FMDV VP4 was inserted into the major immunodominant region. HBc VLPs were also decorated with peptides of the N-terminus of FMDV VP4 attached using a HBc-spike binding tag. Both types of VLPs were used to immunise mice and the resulting serum was investigated for VP4-specific antibodies. The VLP with VP4 inserted into the spike, induced VP4-specific antibodies, however the VLPs with peptides attached to the spikes did not. The VP4-specific antibodies could recognise native FMDV, but virus neutralisation was not demonstrated. This work shows that the HBc VLP presents a useful tool for the presentation of FMDV capsid epitopes.
小核糖核酸病毒口蹄疫病毒(FMDV)是家畜重要经济疾病口蹄疫(FMD)的病原体。VP4是一种高度保守的衣壳蛋白,在病毒进入过程中起重要作用。先前发表的研究表明,靶向小核糖核酸病毒人鼻病毒VP4 N端的抗体具有广泛的中和作用。此外,先前的研究表明,用展示在乙肝核心(HBc)病毒样颗粒(VLP)上的肠道病毒A71 VP4的N端20个氨基酸进行免疫可诱导跨基因型中和。为了研究是否能产生针对FMDV VP4的类似中和反应,设计了展示FMDV VP4 N端的HBc VLP。将FMDV VP4的N端15个氨基酸插入主要免疫优势区域。还用一种HBc-刺突结合标签将FMDV VP4 N端的肽连接到HBc VLP上进行修饰。两种类型的VLP都用于免疫小鼠,并检测所得血清中的VP4特异性抗体。将VP4插入刺突的VLP诱导产生了VP4特异性抗体,然而,在刺突上连接肽的VLP则没有。VP4特异性抗体能够识别天然FMDV,但未证明有病毒中和作用。这项工作表明,HBc VLP是展示FMDV衣壳表位的有用工具。