Jewell J E, Mecham J O
Agricultural Research Service, Arthropod-borne Animal Diseases Research Laboratory, University Station, Laramie, WY 82071.
Virus Res. 1994 Aug;33(2):139-44. doi: 10.1016/0168-1702(94)90050-7.
Genome segment 2, coding for the VP2 protein, of a neutralization resistant variant was compared to segment 2 of the bluetongue virus (BTV) serotype 10 parent from which the variant was derived. Full-length double-stranded cDNA of BTV segment 2 RNA, which was prepared by reverse transcription, was used as template to prepare overlapping subgenomic cDNA products by PCR. Purified PCR cDNA fragments were sequenced by the dideoxy chain termination reaction. Each base was determined an average of 3.7 times. Comparison of the sequence of segment 2 of the neutralization resistant variant with segment 2 of the parental virus showed two base changes, one of which resulted in a changed amino acid. This change was in a different region of VP2 than those previously reported in other neutralization resistant variants of BTV. In addition to this change, both the parental virus and the variant virus differed in two amino acids from the previously published sequence of VP2 of BTV serotype 10.
将一种中和抗性变异株编码VP2蛋白的基因组片段2与该变异株所源自的蓝舌病病毒(BTV)血清型10亲本的片段2进行比较。通过逆转录制备的BTV片段2 RNA的全长双链cDNA用作模板,通过PCR制备重叠的亚基因组cDNA产物。纯化的PCR cDNA片段通过双脱氧链终止反应进行测序。每个碱基平均测定3.7次。将中和抗性变异株的片段2序列与亲本病毒的片段2序列进行比较,发现有两个碱基变化,其中一个导致氨基酸改变。该变化位于VP2的一个与先前报道的BTV其他中和抗性变异株不同的区域。除了这一变化外,亲本病毒和变异病毒在两个氨基酸上也与先前公布的BTV血清型10的VP2序列不同。