Neitzert E, Beck E, de Mello P A, Gomes I, Bergmann I E
Pan American Foot-and-Mouth Disease Center, Rio de Janeiro, Brazil.
Virology. 1991 Oct;184(2):799-804. doi: 10.1016/0042-6822(91)90456-l.
A plasmid has been constructed containing the DNA sequences that direct the expression of the aphthovirus RNA-dependent RNA polymerase (virus infection-associated antigen, VIAA) in its native form. The aphthovirus polypeptide was designed to contain only a single additional amino acid, the N-terminal methionine. The recombinant protein has been purified and used in enzyme-linked immunoelectrotransfer blots to detect aphthovirus-specific antibodies in the sera of persistently infected animals. Furthermore, studies were carried out to test the hypothesis that antibodies against other nonstructural antigens appear in the sera of these animals. It was established that antibodies against polypeptides 3A and 3B can serve as complementary markers for late aphthovirus-carrier state detection. The considerable potential of this approach to detect aphthovirus-specific antibodies, when the isolation of infectious virus is not possible, was demonstrated. Negative results were obtained in animals from virus-free areas and in vaccinated cattle. This assay has the added advantage that no infectious or noninfectious virus is involved during antigen production.
构建了一种质粒,其中包含指导口疮病毒RNA依赖性RNA聚合酶(病毒感染相关抗原,VIAA)以其天然形式表达的DNA序列。口疮病毒多肽被设计为仅包含一个额外的氨基酸,即N端甲硫氨酸。重组蛋白已被纯化,并用于酶联免疫电转移印迹,以检测持续感染动物血清中的口疮病毒特异性抗体。此外,还进行了研究以检验这些动物血清中出现针对其他非结构抗原的抗体这一假设。已确定针对多肽3A和3B的抗体可作为检测晚期口疮病毒携带状态的补充标志物。当无法分离出感染性病毒时,这种检测口疮病毒特异性抗体的方法显示出了巨大潜力。在来自无病毒地区的动物和接种疫苗的牛中获得了阴性结果。该检测方法的另一个优点是在抗原生产过程中不涉及感染性或非感染性病毒。