McGoldrick A, Macadam A J, Dunn G, Rowe A, Burlison J, Minor P D, Meredith J, Evans D J, Almond J W
School of Animal and Microbial Sciences, University of Reading, Whiteknigts, Reading, United Kingdom.
J Virol. 1995 Dec;69(12):7601-5. doi: 10.1128/JVI.69.12.7601-7605.1995.
Of the 55 point mutations which distinguish the type 1 poliovirus vaccine strain (Sabin 1) from its neurovirulent progenitor (P1/Mahoney), two have been strongly implicated by previous studies as determinants of the attenuation phenotype. A change of an A to a G at position 480, located within the 5' noncoding region, has been suggested to be the major attenuating mutation, analogous to the mutations at positions 481 and 472 in poliovirus types 2 and 3, respectively. In addition, the change of a U to a C at position 6203, resulting in an amino acid change in the polymerase protein 3D, has also been implicated as a determinant of attenuation, albeit to a lesser extent. To assess the contributions of these mutations to attenuation and temperature sensitivity, reciprocal changes were generated at these positions in infectious cDNA clones of Sabin 1 and P1/Mahoney. Assays in tissue culture and primates indicated that the two mutations make some contribution to the temperature sensitivity of the Sabin 1 strain but that neither is a strong determinant of attenuation.
在区分1型脊髓灰质炎病毒疫苗株(萨宾1型)与其神经毒力祖代株(P1/马奥尼株)的55个点突变中,先前的研究已强烈表明其中两个突变是减毒表型的决定因素。位于5'非编码区内第480位的A到G的变化被认为是主要的减毒突变,分别类似于2型和3型脊髓灰质炎病毒中第481位和第472位的突变。此外,第6203位的U到C的变化导致聚合酶蛋白3D中的氨基酸变化,也被认为是减毒的一个决定因素,尽管程度较小。为了评估这些突变对减毒和温度敏感性的贡献,在萨宾1型和P1/马奥尼株的感染性cDNA克隆中的这些位置产生了相互变化。组织培养和灵长类动物实验表明,这两个突变对萨宾1型毒株的温度敏感性有一定贡献,但都不是减毒的强决定因素。