Stanway G, Hughes P J, Mountford R C, Reeve P, Minor P D, Schild G C, Almond J W
Proc Natl Acad Sci U S A. 1984 Mar;81(5):1539-43. doi: 10.1073/pnas.81.5.1539.
As part of a study into the molecular basis of attenuation and reversion to neurovirulence in the Sabin poliovirus vaccines, we have determined the complete nucleotide sequence of a cloned DNA copy of the genome of P3/Leon/37, the neurovirulent progenitor of the type 3 Sabin vaccine strain, P3/Leon 12a1b. Comparison of the sequence with that which we previously obtained for the vaccine strain [Stanway, G., Cann, A. J., Hauptmann, R., Hughes, P., Clarke, L. D., Mountford, R. C., Minor, P. D., Schild, G. C. & Almond, J. W. (1983) Nucleic Acids Res. 11, 5629-5643] indicates that attenuation has been brought about by a maximum of 10 point mutations, at least 5 of which are likely to be of minor significance. Predicted amino acid sequences of all the known virus-encoded proteins show that amino acid substitutions have occurred at only three positions. Two of these are in structural proteins (i.e., Ser----Phe in VP3 and Lys----Arg in VP1), and the third, Thr----Ala, is in the nonstructural protein P2-3b. The distribution and nature of nucleotide and amino acid sequence differences suggest that a single base substitution may be responsible for the attenuated phenotype of the vaccine strain.
作为对Sabin脊髓灰质炎病毒疫苗减毒及回复神经毒力分子基础研究的一部分,我们测定了3型Sabin疫苗株P3/Leon 12a1b的神经毒力祖代毒株P3/Leon/37基因组克隆DNA拷贝的完整核苷酸序列。将该序列与我们之前获得的疫苗株序列[Stanway, G., Cann, A. J., Hauptmann, R., Hughes, P., Clarke, L. D., Mountford, R. C., Minor, P. D., Schild, G. C. & Almond, J. W. (1983) Nucleic Acids Res. 11, 5629 - 5643]进行比较,结果表明减毒是由最多10个点突变引起的,其中至少5个可能意义不大。所有已知病毒编码蛋白的预测氨基酸序列显示,仅在三个位置发生了氨基酸替换。其中两个在结构蛋白中(即VP3中的Ser→Phe和VP1中的Lys→Arg),第三个Thr→Ala在非结构蛋白P2 - 3b中。核苷酸和氨基酸序列差异的分布及性质表明,单个碱基替换可能是疫苗株减毒表型的原因。