Ayata M, Kimoto T, Hayashi K, Seto T, Murata R, Ogura H
Department of Medical Zoology, Osaka City University Medical School, Osaka, Japan.
Virus Res. 1998 Mar;54(1):107-15. doi: 10.1016/s0168-1702(98)00012-4.
Measles viruses isolated from brain cells of patients with subacute sclerosing panencephalitis (SSPE) have numerous mutations, especially in the matrix protein (M) gene. To find whether the M genes of these SSPE viruses were mutated randomly or in a pattern, we sequenced this gene from three strains of defective measles virus isolated in Osaka, Japan. We could deduce the sequence of the possible progenitor measles virus for each patient by comparison of the isolate with measles viruses prevailing at roughly the same time and place as the primary infection. Biased hypermutation affected the M genes of all three SSPE viruses, although the molecular mechanisms for the mutations might be various. Replacements of U with C in the plus strand accounted for 76% of all mutations in two of the strains, but in the other strain, replacements of A with G accounted for 52% of the mutations, and the U residues were unchanged.
从亚急性硬化性全脑炎(SSPE)患者脑细胞中分离出的麻疹病毒有许多突变,尤其是在基质蛋白(M)基因中。为了确定这些SSPE病毒的M基因是随机突变还是有规律地突变,我们对从日本大阪分离出的三株缺陷型麻疹病毒的该基因进行了测序。通过将分离株与在初次感染大致相同时间和地点流行的麻疹病毒进行比较,我们可以推断出每位患者可能的始祖麻疹病毒的序列。尽管突变的分子机制可能多种多样,但偏向性超突变影响了所有三株SSPE病毒的M基因。在两株病毒中,正链上U被C取代占所有突变的76%,但在另一株病毒中,A被G取代占突变的52%,U残基未发生变化。