Su W, Gao J, Zang Y, Wu H, Wang L, Hu H, Yu X, Kong W, Jiang C
Acta Virol. 2015 Mar;59(1):33-9. doi: 10.4149/av_2015_01_33.
Norovirus (NoV) is the main cause of nonbacterial infectious gastroenteritis. Due to the difficulty of culturing the virus, research on vaccine against NoV is focused on virus-like particles (VLPs). On the other hand, the P particles assembled from the P domains of NoV capsid protein become a promising vaccine candidate. GII.4 is the most prevalent genotype of NoV. While the immunogenicity of P particles derived from the GII.4 1996 variant has been investigated, the research on P particles of more recently prevalent variants is lacking. In this study, the P domain of the capsid protein of GII.4 genotype 2004 variant was expressed in Escherichia coli, purified and auto-assembled into P particles of 14-25 nm. Immunization with P particles induced specific serum antibodies with titers of 245,600 and 145,700 in mice and rabbits, respectively. The GII.4 NoV 2004 variant bound to type A, B and O secretor-positive saliva and immune sera blocked this binding, suggesting induction of neutralizing activity in such sera. Thus, this study demonstrated the immunogenicity of NoV P particles generated from E. coli and provided evidence supporting the development of this approach.
诺如病毒(NoV)是非细菌性感染性肠胃炎的主要病因。由于该病毒培养困难,针对诺如病毒的疫苗研究主要集中在病毒样颗粒(VLP)上。另一方面,由诺如病毒衣壳蛋白的P结构域组装而成的P颗粒成为一种有前景的疫苗候选物。GII.4是诺如病毒最常见的基因型。虽然已对源自GII.4 1996变异株的P颗粒的免疫原性进行了研究,但对最近流行变异株的P颗粒研究较少。在本研究中,GII.4基因型2004变异株衣壳蛋白的P结构域在大肠杆菌中表达、纯化并自动组装成14 - 25纳米的P颗粒。用P颗粒免疫分别在小鼠和兔子中诱导出效价为245,600和145,700的特异性血清抗体。GII.4诺如病毒2004变异株与A、B和O分泌型阳性唾液结合,免疫血清可阻断这种结合,表明此类血清中诱导出了中和活性。因此,本研究证明了由大肠杆菌产生的诺如病毒P颗粒的免疫原性,并为支持这种方法的开发提供了证据。