Fleming S B, Lyttle D J, Sullivan J T, Mercer A A, Robinson A J
Health Research Council Virus Research Unit, University of Otago, Dunedin, New Zealand.
J Gen Virol. 1995 Dec;76 ( Pt 12):2969-78. doi: 10.1099/0022-1317-76-12-2969.
Restriction endonuclease analysis of the DNA extracted orf virus strain NZ2, which had been serially passaged in primary bovine testis cells, revealed a population of variants that had over-grown the wild-type virus. At least three distinct mutant forms were identified in which the right end of the genome had been duplicated and translocated to the left end, accompanied by deletions of sequences at the left end. Sequencing of a single variant isolated from the heterogeneous population revealed that recombination had occurred between non-homologous sequences. In this case, 6.6 kb of DNA at the left end of the genome had been replaced by 19.3 kb from the right end. The transposition resulted in the deletion at the left end of 3.3 kb of DNA encoding three genes and the terminal sequences of a fourth gene. The three genes completely deleted were a homologue of dUTPase, a gene that encodes a protein containing ankyrin-like repeats and a homologue of the 5K gene of the vaccinia virus WR strain. Experimental inoculation of sheep showed that the genes are also non-essential in vivo, but that the size of the lesion was reduced, compared with that induced by the wild-type, and resolved more rapidly.
对在原代牛睾丸细胞中连续传代的orf病毒株NZ2提取的DNA进行限制性内切酶分析,结果显示存在一群数量超过野生型病毒的变异体。鉴定出至少三种不同的突变形式,其中基因组的右端被复制并转移到左端,同时左端的序列发生缺失。对从异质群体中分离出的单个变异体进行测序表明,非同源序列之间发生了重组。在这种情况下,基因组左端的6.6 kb DNA被右端的19.3 kb所取代。这种转座导致左端缺失了3.3 kb编码三个基因和第四个基因末端序列的DNA。完全缺失的三个基因分别是dUTPase的同源物、一个编码含有锚蛋白样重复序列的蛋白质的基因以及痘苗病毒WR株5K基因的同源物。对绵羊进行实验性接种表明,这些基因在体内也是非必需的,但与野生型诱导的损伤相比,损伤的大小减小,且愈合更快。