Iizuka N, Kohara M, Hagino-Yamagishi K, Abe S, Komatsu T, Tago K, Arita M, Nomoto A
Department of Microbiology, Tokyo Metropolitan Institute of Medical Science, Japan.
J Virol. 1989 Dec;63(12):5354-63. doi: 10.1128/JVI.63.12.5354-5363.1989.
Viral attenuation may be due to lowered efficiency of certain steps essential for viral multiplication. For the construction of less neurovirulent strains of poliovirus in vitro, we introduced deletions into the 5' noncoding sequence (742 nucleotides long) of the genomes of the Mahoney and Sabin 1 strains of poliovirus type 1 by using infectious cDNA clones of the virus strains. Plaque sizes shown by deletion mutants were used as a marker for rate of viral proliferation. Deletion mutants of both the strains thus constructed lacked a genome region of nucleotide positions 564 to 726. The sizes of plaques displayed by these deletion mutants were smaller than those by the respective parental viruses, although a phenotype referring to reproductive capacity at different temperatures (rct) of viruses was not affected by introduction of the deletion. Monkey neurovirulence tests were performed on the deletion mutants. The results clearly indicated that the deletion mutants had much less neurovirulence than with the corresponding parent viruses. Production of infectious particles and virus-specific protein synthesis in cells infected with the deletion mutants started later than in those infected with the parental viruses. The rate at which cytopathic effect progressed was also slower in cells infected with the mutants. Phenotypic stability of the deletion mutant for small-plaque phenotype and temperature sensitivity was investigated after passaging the mutant at an elevated temperature of 37.5 degrees C. Our data strongly suggested that the less neurovirulent phenotype introduced by the deletion is very stable during passaging of the virus.
病毒减毒可能是由于病毒增殖所必需的某些步骤的效率降低。为了在体外构建神经毒性较低的脊髓灰质炎病毒株,我们通过使用病毒株的感染性 cDNA 克隆,对 1 型脊髓灰质炎病毒 Mahoney 株和 Sabin 1 株基因组的 5' 非编码序列(742 个核苷酸长)进行了缺失。缺失突变体所显示的噬斑大小被用作病毒增殖速率的标志物。由此构建的两种毒株的缺失突变体都缺少核苷酸位置 564 至 726 的基因组区域。这些缺失突变体所显示的噬斑大小比各自的亲本病毒小,尽管引入缺失对病毒在不同温度下的繁殖能力(rct)表型没有影响。对缺失突变体进行了猴神经毒性试验。结果清楚地表明,缺失突变体的神经毒性比相应的亲本病毒小得多。感染缺失突变体的细胞中感染性颗粒的产生和病毒特异性蛋白质的合成比感染亲本病毒的细胞开始得晚。感染突变体的细胞中细胞病变效应进展的速率也较慢。在 37.5 摄氏度的高温下传代突变体后,研究了缺失突变体小噬斑表型和温度敏感性的表型稳定性。我们的数据强烈表明,缺失引入的较低神经毒性表型在病毒传代过程中非常稳定。