Cann A J, Stanway G, Hughes P J, Minor P D, Evans D M, Schild G C, Almond J W
Nucleic Acids Res. 1984 Oct 25;12(20):7787-92. doi: 10.1093/nar/12.20.7787.
The complete nucleotide sequence has been determined of a strain of poliovirus type 3, P3/119, isolated from the central nervous system of a victim of fatal vaccine-associated poliomyelitis. Comparison of this sequence with those obtained previously for the Sabin type 3 vaccine, P3/Leon 12a1b and its neurovirulent progenitor, P3/Leon/37, reveals that these three strains are on a direct geneaological lineage and therefore that P3/119 is a bona fide revertant of the vaccine. P3/119 differs in sequence from its attenuated vaccine parent at just seven positions. Only one of these differences, a mutation from U to C at position 472 in the presumed noncoding region of the genome, is a back mutation to the wild type sequence. Of the six other differences, three give rise to coding changes in virus structural proteins, two are silent changes in the major open reading frame of the genome and one affects the 3'-terminus just prior to the poly A tract. These differences indicate that there are three possible types of molecular change which could, singly or collectively, result in attenuation and reversion to neurovirulence of the Sabin type 3 vaccine.
已确定从一名致命的疫苗相关脊髓灰质炎受害者中枢神经系统分离出的3型脊髓灰质炎病毒株P3/119的完整核苷酸序列。将该序列与先前获得的Sabin 3型疫苗P3/Leon 12a1b及其神经毒力祖代P3/Leon/37的序列进行比较,发现这三个毒株处于直接的谱系中,因此P3/119是该疫苗真正的回复突变株。P3/119与其减毒疫苗亲本的序列仅在七个位置上存在差异。这些差异中只有一个,即在基因组假定的非编码区第472位从U突变为C,是向野生型序列的回复突变。在其他六个差异中,三个导致病毒结构蛋白的编码变化,两个是基因组主要开放阅读框中的沉默变化,一个影响紧接在多聚A序列之前的3'末端。这些差异表明存在三种可能的分子变化类型,它们单独或共同作用,可能导致Sabin 3型疫苗的减毒和向神经毒力的回复。