Ito H, Minamoto N, Goto H, Luo T R, Sugiyama M, Kinjo T
Department of Veterinary Public Health, Faculty of Agriculture, Gifu University, Japan.
Arch Virol. 1996;141(11):2129-38. doi: 10.1007/BF01718220.
The cDNA encoding the VP6 gene of avian rotavirus PO-13 strain was inserted into the bacterial expression vector pET-3a. Upon isopropyl-1-thio-beta-D-galactoside induction, the E. coli BL21 (DE3) harboring the vector containing cDNA of the VP6 gene produced an approximately 45-kDa polypeptide, which reacted with rabbit serum against PO-13 strain in Western blotting. To study the antigenic sites on VP6, various deletion mutants were constructed, expressed in E. coli and the reactivity with antigenic site I- and II-specific MAbs analyzed by Western blotting. Site I, which is shared with all group A mammalian and avian rotaviruses except for chicken rotavirus, was found to be located at amino acid positions 45 to 65, and site II, which probably contributes to an authentic group A antigen common to both mammalian and avian rotaviruses, at amino acid positions 134 to 142.
将编码禽轮状病毒PO - 13株VP6基因的cDNA插入细菌表达载体pET - 3a。经异丙基 - 1 - 硫代 - β - D - 半乳糖苷诱导后,携带含有VP6基因cDNA载体的大肠杆菌BL21(DE3)产生了一条约45 kDa的多肽,该多肽在蛋白质印迹法中与抗PO - 13株的兔血清发生反应。为了研究VP6上的抗原位点,构建了各种缺失突变体,在大肠杆菌中表达,并通过蛋白质印迹法分析其与抗原位点I和II特异性单克隆抗体的反应性。发现位点I位于氨基酸位置45至65,所有A组哺乳动物和禽轮状病毒(除鸡轮状病毒外)都共有该位点;位点II位于氨基酸位置134至142,它可能是哺乳动物和禽轮状病毒共有的真正A组抗原的组成部分。