Characterization of the subunit particles of feline calicivirus.

Y Tohya, M Tsubakimoto, T Horimoto, E Takahashi, T Mikami
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引用次数: 6

Abstract

In the culture fluid from cells infected with feline calicivirus (FCV) F4 strain, the infectious and smaller non-infectious subunit particles were detected by complement fixation (CF) test after sucrose gradient centrifugation. The results of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblot analyses confirmed the existence of the subunit particles of FCV, and showed that the infectious and subunit particles were mainly composed of 65K capsid protein. The subunit particles were further purified by ion-exchange chromatography and sucrose gradient centrifugation. The purified subunit and infectious particles had the same neutralizing epitope on 65K protein detected by immunoblot analysis with a neutralizing monoclonal antibody. Antigenic comparison between the infectious and subunit particles by the CF tests using an antiserum against heterologous strain of FCV F14 indicated that the subunit particles might have more highly conserved antigens of FCV than the infectious particles.

猫杯状病毒亚基颗粒的表征。
在感染猫杯状病毒(FCV) F4株的细胞培养液中,经蔗糖梯度离心,用补体固定法(CF)检测感染性和较小的非感染性亚基颗粒。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和免疫印迹分析结果证实了FCV亚基颗粒的存在,并表明感染性和亚基颗粒主要由65K衣壳蛋白组成。通过离子交换层析和蔗糖梯度离心进一步纯化亚基颗粒。免疫印迹法检测纯化亚基与感染颗粒在65K蛋白上具有相同的中和表位。用FCV异源株F14抗血清对感染性颗粒和亚单位颗粒进行抗原比较,结果表明亚单位颗粒可能比感染性颗粒具有更多高度保守的FCV抗原。
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