Nichol S T, Rowe J E, Fitch W M
Cell and Molecular Biology Program, School of Veterinary Medicine, University of Nevada, Reno 89557.
Virology. 1989 Feb;168(2):281-91. doi: 10.1016/0042-6822(89)90268-7.
A T1 ribonuclease fingerprinting study of a large number of virus isolates had previously demonstrated that considerable genetic variability existed among natural isolates of the vesicular stomatitis virus (VSV) New Jersey (NJ) serotype [S.T. Nichol (1988) J. Virol. 62, 572-579]. Based on these results, 34 virus isolates were chosen as representing the extent of genetic diversity within the VSV NJ serotype. We report the entire glycoprotein (G) gene nucleotide sequence and the deduced amino acid sequence for each of these viruses. Up to 19.8% G gene sequence differences could be seen among NJ serotype isolates. Analysis of the distribution of nucleotide substitutions relative to nucleotide codon position revealed that third position changes were distributed randomly throughout the gene. Third base changes constituted 84% of the observed nucleotide substitutions and affected 89% of the third base positions located in the G gene. Only three short oligonucleotide stretches of complete sequence conservation were observed. The remaining nucleotide changes located in the first and second positions were not distributed randomly, indicating that most of the amino acids coded by the G gene cannot be altered without reducing the fitness of the VSV NJ serotype viruses. Despite these constraints, up to 8.5% amino acid differences were observed between virus isolates. These differences were located throughout the G protein including regions adjacent to defined major antibody neutralization epitopes. Apparent clusters of amino acid substitutions were present in the hydrophobic signal sequence, transmembrane domain, and within the cytoplasmic domain of the G protein. A maximum parsimony analysis of the G gene nucleotide sequences allowed construction of a phylogram indicating the evolutionary relationship of these viruses. The VSV NJ serotype appears to contain at least three distinct lineages or subtypes. All recent virus isolates from the United States and Mexico are within subtype I and appear to have evolved from an ancestor more closely related to the Hazelhurst historic strain than other older strains. The implications of these findings for the evolution, epizootiology, and classification of these viruses are discussed.
先前一项针对大量病毒分离株的T1核糖核酸酶指纹图谱研究表明,水疱性口炎病毒(VSV)新泽西(NJ)血清型的天然分离株之间存在相当大的遗传变异性[S.T. 尼科尔(1988年)《病毒学杂志》62卷,572 - 579页]。基于这些结果,选择了34个病毒分离株来代表VSV NJ血清型内的遗传多样性程度。我们报告了这些病毒中每一个的完整糖蛋白(G)基因核苷酸序列以及推导的氨基酸序列。在NJ血清型分离株之间可观察到高达19.8%的G基因序列差异。相对于核苷酸密码子位置的核苷酸替换分布分析表明,第三位的变化在整个基因中随机分布。第三位碱基变化占观察到的核苷酸替换的84%,并影响了位于G基因中的89%的第三位碱基位置。仅观察到三个短的完全序列保守的寡核苷酸片段。位于第一位和第二位的其余核苷酸变化并非随机分布,这表明G基因编码的大多数氨基酸在不降低VSV NJ血清型病毒适应性的情况下不能改变。尽管有这些限制,但在病毒分离株之间仍观察到高达8.5%的氨基酸差异。这些差异分布在整个G蛋白中,包括与确定的主要抗体中和表位相邻的区域。在G蛋白的疏水信号序列、跨膜结构域和细胞质结构域内存在明显的氨基酸替换簇。对G基因核苷酸序列进行的最大简约分析允许构建一个系统发育树,表明这些病毒的进化关系。VSV NJ血清型似乎包含至少三个不同的谱系或亚型。来自美国和墨西哥的所有近期病毒分离株都属于亚型I,并且似乎是从一个比其他较老菌株更接近黑泽赫斯特历史菌株的祖先进化而来的。讨论了这些发现对这些病毒的进化、动物流行病学和分类的影响。