Stanway G, Cann A J, Hauptmann R, Mountford R C, Clarke L D, Reeve P, Minor P D, Schild G C, Almond J W
Eur J Biochem. 1983 Oct 3;135(3):529-33. doi: 10.1111/j.1432-1033.1983.tb07684.x.
Three closely related strains of poliovirus type 3 have been used to study the molecular basis of attenuation in the currently used Sabin vaccine of this serotype. Plaque-purified derivatives of these strains possess closely similar serological and biochemical properties yet differ markedly in neurovirulence for monkeys. Molecular cloning via an RNA . cDNA method has facilitated comparative nucleotide sequencing. Initial efforts have concentrated on the region of the genome encoding VP1. Only minor structural differences between neurovirulent and attenuated type 3 strains were detected, in contrast to the major differences observed between the vaccine strains of poliovirus type 1 and its virulent precursor P1/Mahoney. These observations suggest that the molecular basis of attenuation of type 3 Sabin vaccine virus does not involve the VP1 polypeptide and, therefore, that mutations conferring the attenuated phenotype probably lie elsewhere in the genome.
已使用三种密切相关的3型脊髓灰质炎病毒株来研究当前使用的该血清型萨宾疫苗中减毒的分子基础。这些毒株的空斑纯化衍生物具有极为相似的血清学和生化特性,但对猴子的神经毒力却有显著差异。通过RNA.cDNA方法进行的分子克隆有助于进行比较核苷酸测序。最初的研究集中在基因组中编码VP1的区域。与1型脊髓灰质炎病毒疫苗株及其强毒株前体P1/马奥尼之间观察到的主要差异形成对比的是,在神经毒力强和减毒的3型毒株之间仅检测到微小的结构差异。这些观察结果表明,3型萨宾疫苗病毒减毒的分子基础不涉及VP1多肽,因此,赋予减毒表型的突变可能位于基因组的其他位置。