Kanno T, Mackay D, Inoue T, Wilsden G, Yamakawa M, Yamazoe R, Yamaguchi S, Shirai J, Kitching P, Murakami Y
Department of Exotic Disease, National Institute of Animal Health, 6-20-1, Josuihoncho, Kodaira, Tokyo 187-0022, Japan.
J Virol. 1999 Apr;73(4):2710-6. doi: 10.1128/JVI.73.4.2710-2716.1999.
A series of recombinant viruses were constructed using infectious cDNA clones of the virulent J1'73 (large plaque phenotype) and the avirulent H/3'76 (small plaque phenotype) strains of swine vesicular disease virus to identify the genetic determinants of pathogenicity and plaque phenotype. Both traits could be mapped to the region between nucleotides (nt) 2233 and 3368 corresponding to the C terminus of VP3, the whole of VP1, and the N terminus of 2A. In this region, there are eight nucleotide differences leading to amino acid changes between the J1'73 and the H/3'76 strains. Site-directed mutagenesis of individual nucleotides from the virulent to the avirulent genotype and vice versa indicated that A at nt 2832, encoding glycine at VP1-132, and G at nt 3355, encoding arginine at 2APRO-20, correlated with a large-plaque phenotype and virulence in pigs, irrespective of the origin of the remainder of the genome. Of these two sites, 2APRO-20 appeared to be the dominant determinant for the large-plaque phenotype but further studies are required to elucidate their relative importance for virulence in pigs.
利用猪水疱病病毒强毒株J1'73(大噬斑表型)和无毒株H/3'76(小噬斑表型)的感染性cDNA克隆构建了一系列重组病毒,以确定致病性和噬斑表型的遗传决定因素。这两个性状都可定位到对应于VP3 C末端、整个VP1和2A N末端的核苷酸(nt)2233至3368之间的区域。在该区域,J1'73株和H/3'76株之间有八个核苷酸差异导致氨基酸变化。从强毒株基因型到无毒株基因型以及反之的单个核苷酸定点诱变表明,nt 2832处的A(在VP1-132编码甘氨酸)和nt 3355处的G(在2APRO-20编码精氨酸)与大噬斑表型和猪的毒力相关,而与基因组其余部分的来源无关。在这两个位点中,2APRO-20似乎是大噬斑表型的主要决定因素,但需要进一步研究以阐明它们对猪毒力的相对重要性。