Matsui S M, Kim J P, Greenberg H B, Young L M, Smith L S, Lewis T L, Herrmann J E, Blacklow N R, Dupuis K, Reyes G R
Department of Medicine (Gastroenterology), Stanford University School of Medicine, California 94305.
J Virol. 1993 Mar;67(3):1712-5. doi: 10.1128/JVI.67.3.1712-1715.1993.
We report the cloning of antigenic, protein-coding regions of human astrovirus serotype 1 that appear to be common to most, if not all, serotypes of human astrovirus. Screening of lambda gt11 libraries identified three different but overlapping clones (A43, A35, and A1) and one independent clone (A14) that reacted with serum from a rabbit repeatedly immunized with purified astrovirus particles but not with its preimmunization serum. These clones were shown to be astrovirus specific. Of note, a radiolabeled probe representing the immunoreactive clones A43-A35-A1 hybridized exclusively to the 7.2-kb astrovirus genomic RNA, while a clone A14-specific probe hybridized with both the genomic and the 2.8-kb astrovirus subgenomic RNAs. This suggests that the immunoreactive epitopes, selected by antiserum to purified astrovirus particles, are encoded by the subgenomic RNA as well as other regions of the genomic RNA.
我们报告了人类1型星状病毒抗原性蛋白质编码区的克隆,这些区域似乎是大多数(如果不是全部)人类星状病毒血清型所共有的。对λgt11文库的筛选鉴定出三个不同但相互重叠的克隆(A43、A35和A1)以及一个独立克隆(A14),它们与用纯化星状病毒颗粒反复免疫的兔血清发生反应,但不与其免疫前血清发生反应。这些克隆被证明是星状病毒特异性的。值得注意的是,代表免疫反应性克隆A43 - A35 - A1的放射性标记探针仅与7.2 kb的星状病毒基因组RNA杂交,而克隆A14特异性探针则与基因组RNA和2.8 kb的星状病毒亚基因组RNA都杂交。这表明,由抗纯化星状病毒颗粒血清选择的免疫反应性表位由亚基因组RNA以及基因组RNA的其他区域编码。