Cha T A, Tom E, Kemble G W, Duke G M, Mocarski E S, Spaete R R
Aviron, Burlingame, California 94010, USA.
J Virol. 1996 Jan;70(1):78-83. doi: 10.1128/JVI.70.1.78-83.1996.
Nucleotide sequence comparisons were performed on a highly heterogeneous region of three human cytomegalovirus strains, Toledo, Towne, and AD169. The low-passage, virulent Toledo genome contained a DNA segment of approximately 13 kbp that was not found in the Towne genome and a segment of approximately 15 kbp that was not found in the AD169 genome. The Towne strain contained approximately 4.7 kbp of DNA that was absent from the AD169 genome, and only about half of this segment was present, arranged in an inverted orientation, in the Toledo genome. These additional sequences were located at the unique long (UL)/b' (IRL) boundary within the L component of the viral genome. A region representing nucleotides 175082 to 178221 of the AD169 genome was conserved in all three strains; however, substantial reduction in the size of the adjacent b' sequence was found. The additional DNA segment within the Toledo genome contained 19 open reading frames not present in the AD169 genome. The additional DNA segment within the Towne genome contained four new open reading frames, only one of which shared homology with the Toledo genome. This comparison was extended to five additional clinical isolates, and the additional Toledo sequence was conserved in all. These findings reveal a dramatic level of genome sequence complexity that may explain the differences that these strains exhibit in virulence and tissue tropism. Although the additional sequences have not altered the predicted size of the viral genome (230 to 235 kbp), a total of 22 new open reading frames (denoted UL133 to UL154), many of which have sequence characteristics of glycoproteins, are now defined as cytomegalovirus specific. Our work suggests that wild-type virus carries more than 220 genes, some of which are lost by large-scale deletion and rearrangement of the UL/b' region during laboratory passage.
对三株人巨细胞病毒毒株托莱多(Toledo)、汤氏(Towne)和AD169的一个高度异质区域进行了核苷酸序列比较。低传代、有致病性的托莱多基因组包含一段约13 kbp的DNA片段,该片段在汤氏基因组中未发现,还有一段约15 kbp的片段,在AD169基因组中未发现。汤氏毒株含有约4.7 kbp的AD169基因组中不存在的DNA,并且该片段中只有约一半以反向排列存在于托莱多基因组中。这些额外的序列位于病毒基因组L组分内的独特长片段(UL)/b'(内部反向重复长片段,IRL)边界处。代表AD169基因组第175082至178221位核苷酸的区域在所有三株毒株中都是保守的;然而,发现相邻的b'序列大小大幅减小。托莱多基因组内的额外DNA片段包含19个AD169基因组中不存在的开放阅读框。汤氏基因组内的额外DNA片段包含4个新的开放阅读框,其中只有1个与托莱多基因组具有同源性。这种比较扩展到另外5株临床分离株,并且所有分离株中都保留了托莱多的额外序列。这些发现揭示了基因组序列复杂性的显著程度,这可能解释了这些毒株在毒力和组织嗜性方面表现出的差异。尽管这些额外序列没有改变病毒基因组的预测大小(230至235 kbp),但现在总共定义了22个新的开放阅读框(命名为UL133至UL154),其中许多具有糖蛋白的序列特征,属于巨细胞病毒特异性。我们的研究表明,野生型病毒携带超过220个基因,其中一些基因在实验室传代过程中因UL/b'区域的大规模缺失和重排而丢失。