Water Pollution Research Department, Environmental Research Division, National Research Centre, Dokki, Cairo, Egypt.
Int J Biol Macromol. 2013 Aug;59:67-71. doi: 10.1016/j.ijbiomac.2013.04.003. Epub 2013 Apr 12.
The middle capsid protein of rotavirus, VP6, constitutes approximately 51% of the virion by weight. The high degree of identity (>87-99%) in the primary amino acid sequences of VP6 proteins from mammalian rotaviruses suggests VP6-based vaccines could potentially provide heterotypic protection. For this reason, significant effort has been directed toward producing recombinant rotavirus VP6 vaccines. We have cloned and expressed 155bp of the VP6 most frequent in Egyptian rotavirus sewage isolates, encoding the VP6 protein in the pET30b vector having an apparent molecular mass of 12.5kDa. The recombinant VP6 expressed by the transformants was detected by SDS-PAGE analysis. Rabbits immunized with the recombinant rotavirus expressed VP6 elicited VP6-specific IgG antibodies that provided significant reductions in the infectious units of the Egyptian rotavirus sewage isolate and human reference rotavirus Wa strain in vitro assay.
轮状病毒的中间衣壳蛋白 VP6 占病毒粒子重量的约 51%。哺乳动物轮状病毒 VP6 蛋白的一级氨基酸序列的高度同源性(>87-99%)表明,基于 VP6 的疫苗有可能提供异型保护。出于这个原因,人们已经投入大量精力生产重组轮状病毒 VP6 疫苗。我们已经克隆并表达了埃及轮状病毒污水分离株中最常见的 VP6 的 155bp,在 pET30b 载体中编码 VP6 蛋白,其表观分子量为 12.5kDa。转化子表达的重组 VP6 通过 SDS-PAGE 分析检测到。用重组轮状病毒表达的 VP6 免疫的兔子诱导产生了 VP6 特异性 IgG 抗体,在体外试验中显著降低了埃及轮状病毒污水分离株和人参考轮状病毒 Wa 株的感染单位。