Iwata N, Fujino M, Tuchiya K, Iwata A, Otaki Y, Ueda S
Nippon Institute for Biological Science, Tokyo, Japan.
J Vet Med Sci. 1998 Feb;60(2):175-80. doi: 10.1292/jvms.60.175.
Recombinant baculoviruses were constructed to express the putative proteins VP1, VP2 or VP3 of the chicken anemia virus (CAV). The recombinant VP1, VP2 or VP3 were detected by SDS-PAGE, and their molecular weights were 50, 30/27 and 16 kDa, respectively. The VP2 and VP3 reacted with sera from CAV-infected chickens in Western blot analysis and when used as an enzyme-linked immunosorbent assay (ELISA) antigen, but VP1 did not. Antibodies to CAV were detected, by ELISA using crude insect cell lysates containing VP2 or VP3, from 2 to 20 weeks or 2 to 7 weeks after CAV infection, respectively. These findings indicate that recombinant VP2 and VP3 expressed in the baculovirus vector system can be used as antigens to detect anti-CAV antibodies in ELISA.
构建重组杆状病毒以表达鸡贫血病毒(CAV)的假定蛋白VP1、VP2或VP3。通过SDS-PAGE检测重组VP1、VP2或VP3,其分子量分别为50 kDa、30/27 kDa和16 kDa。在蛋白质印迹分析中,VP2和VP3与CAV感染鸡的血清发生反应,并且当用作酶联免疫吸附测定(ELISA)抗原时,VP1则不会。分别在CAV感染后2至20周或2至7周,通过ELISA使用含有VP2或VP3的粗昆虫细胞裂解物检测到了针对CAV的抗体。这些发现表明,在杆状病毒载体系统中表达的重组VP2和VP3可以用作抗原,在ELISA中检测抗CAV抗体。