Mustafa Suhaili, Abd-Aziz Noraini, Saw Wuan-Ting, Liew Sien-Yei, Yusoff Khatijah, Shafee Norazizah
Department of Animal Science and Fishery, Universiti Putra Malaysia, Bintulu Sarawak Campus, Bintulu 97008, Malaysia.
Centre for Virus and Vaccine Research (CVVR), School of Science and Technology, Sunway University, Subang Jaya 47500, Malaysia.
Vaccines (Basel). 2020 Dec 7;8(4):742. doi: 10.3390/vaccines8040742.
Enterovirus 71 (EV71) is the major causative agent in hand, foot, and mouth disease (HFMD), and it mainly infects children worldwide. Despite the risk, there is no effective vaccine available for this disease. Hence, a recombinant protein construct of truncated nucleocapsid protein viral protein 1 (NPt-VP1), which is capable of inducing neutralizing antibody against EV71, was evaluated in a mouse model. Truncated nucleocapsid protein Newcastle disease virus that was used as immunological carrier fused to VP1 of EV71 as antigen. The recombinant plasmid carrying corresponding genes was constructed by recombinant DNA technology and the corresponding protein was produced in expression system. The recombinant NPt-VP1 protein had elicited neutralizing antibodies against EV71 with the titer of 1:16, and this result is higher than the titer that is elicited by VP1 protein alone (1:8). It was shown that NPt containing immunogenic epitope(s) of VP1 was capable of inducing a greater functional immune response when compared to full-length VP1 protein alone. It was capable to carry larger polypeptide compared to full-length NP protein. The current study also proved that NPt-VP1 protein can be abundantly produced in recombinant protein form by expression system. The findings from this study support the importance of neutralizing antibodies in EV71 infection and highlight the potential of the recombinant NPt-VP1 protein as EV71 vaccine.
肠道病毒71型(EV71)是手足口病(HFMD)的主要病原体,全球范围内主要感染儿童。尽管存在风险,但尚无针对该疾病的有效疫苗。因此,在小鼠模型中评估了一种能够诱导抗EV71中和抗体的截短核衣壳蛋白病毒蛋白1(NPt-VP1)重组蛋白构建体。截短的新城疫病毒核衣壳蛋白用作免疫载体,与EV71的VP1作为抗原融合。通过重组DNA技术构建携带相应基因的重组质粒,并在表达系统中产生相应蛋白。重组NPt-VP1蛋白诱导出了效价为1:16的抗EV71中和抗体,该结果高于单独VP1蛋白诱导出的效价(1:8)。结果表明,与单独的全长VP1蛋白相比,含有VP1免疫原性表位的NPt能够诱导更强的功能性免疫反应。与全长NP蛋白相比,它能够携带更大的多肽。本研究还证明,NPt-VP1蛋白可以通过表达系统以重组蛋白形式大量产生。本研究结果支持了中和抗体在EV71感染中的重要性,并突出了重组NPt-VP1蛋白作为EV71疫苗的潜力。