Mackow E R, Werner-Eckert R, Fay M E, Tao H, Chen G
Northport Veterans Administration Medical Center, New York 11768.
J Virol. 1993 May;67(5):2730-8. doi: 10.1128/JVI.67.5.2730-2738.1993.
A complete cDNA copy of the fourth RNA segment of the human group B rotavirus adult diarrheal rotavirus (ADRV) has been cloned into lambda phage and excised into plasmid pSK Bluescript. Gene segment 4 contains 2,303 bases and encodes one long open reading frame beginning at base 16 and terminating at base 2263. The encoded protein contains 749 amino acids, with a calculated molecular mass of 84.4 kDa and a pI of 6.1. Gene 4 cDNA was inserted into a recombinant baculovirus via homologous recombination. The gene 4 polypeptide migrates at 84 kDa when expressed either by a recombinant baculovirus or in vitro in a rabbit reticulocyte lysate. The gene 4 protein is immunoprecipitable by hyperimmune serum to ADRV, human ADRV convalescent-phase serum, a porcine group B rotavirus infection serum, and a monoclonal antibody made to ADRV virion. Guinea pig hyperimmune serum to the baculovirus-expressed ADRV VP4 protein recognizes virus and immunoprecipitates an 84-kDa protein from in vitro translations of total ADRV mRNA. In addition, the gene 4-encoded protein shares significant amino acid identity and similarity with the group A rotavirus VP4 protein. This information, together with our previous identification of an 84-kDa protein present on iodinated intact virion but not EDTA-treated ADRV, suggests that gene 4 encodes the VP4 protein equivalent present on the outer capsid of ADRV. The ADRV VP4 protein is also 58% identical to the IDIR rat group B rotavirus gene segment 3 protein. The substantial differences between these two group B VP4 proteins suggests that they are distantly related and likely to define two different group B rotavirus VP4 serotypes. The baculovirus-expressed VP4 protein should be useful for developing serotyping reagents and tests for human and animal group B rotaviruses as well as for addressing the role of VP4 in ADRV neutralization.
人B组轮状病毒成人腹泻轮状病毒(ADRV)的第四RNA片段的完整cDNA拷贝已被克隆到λ噬菌体中,并切割到质粒pSK Bluescript中。基因片段4含有2303个碱基,编码一个长开放阅读框,起始于第16个碱基,终止于第2263个碱基。编码的蛋白质含有749个氨基酸,计算分子量为84.4 kDa,pI为6.1。基因4 cDNA通过同源重组插入重组杆状病毒中。当通过重组杆状病毒或在兔网织红细胞裂解物中体外表达时,基因4多肽迁移率为84 kDa。基因4蛋白可被ADRV超免疫血清、人ADRV恢复期血清、猪B组轮状病毒感染血清以及针对ADRV病毒体产生的单克隆抗体免疫沉淀。针对杆状病毒表达的ADRV VP4蛋白的豚鼠超免疫血清可识别病毒,并从总ADRV mRNA的体外翻译产物中免疫沉淀出一种84 kDa的蛋白。此外,基因4编码的蛋白与A组轮状病毒VP4蛋白具有显著的氨基酸同一性和相似性。这些信息,连同我们之前鉴定出的存在于碘化完整病毒体上但不存在于经EDTA处理的ADRV上的一种84 kDa蛋白,表明基因4编码ADRV外膜上的等效VP4蛋白。ADRV VP4蛋白与IDIR大鼠B组轮状病毒基因片段3蛋白也有58%的同一性。这两种B组VP4蛋白之间的显著差异表明它们关系较远,可能定义了两种不同的B组轮状病毒VP4血清型。杆状病毒表达的VP4蛋白应有助于开发用于人和动物B组轮状病毒的血清分型试剂和检测方法,以及研究VP4在ADRV中和中的作用。