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猫杯状病毒在猫持续感染期间的表型和基因型变异

Phenotypic and genotypic variation of feline calicivirus during persistent infection of cats.

作者信息

Kreutz L C, Johnson R P, Seal B S

机构信息

Virology Swine Research Unit, National Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Ames, IA 50010, USA.

出版信息

Vet Microbiol. 1998 Jan 16;59(2-3):229-36. doi: 10.1016/s0378-1135(97)00158-2.

Abstract

Amino acid sequence of the capsid protein hypervariable region of nine feline calicivirus (FCV) isolates recovered from cats persistently infected after inoculation with the FCV strain 255 parent virus is reported. Capsid proteins from all the isolates were highly cross reactive by Western blot analysis using polyclonal antisera to FCV. Reverse-transcription PCR was used to obtain sequence information of the FCV capsid protein highly variable E region. Amino acid substitutions occurred between residues 426 and 458 of the FCV capsid protein E region. The sequence data and phylogenetic reconstructions based on the sequence information correlated well with antigenic differences among isolates determined by two-way cross neutralization. These results agree with previous reports using divergent isolates of FCV that correlated amino acid differences with serology. This further supports the hypothesis that the FCV capsid protein E region from residues 426 to 458 contains the serotypic determinants of FCV important to antigenic variation.

摘要

报道了从接种猫杯状病毒(FCV)毒株255亲本病毒后持续感染的猫中分离出的9株FCV衣壳蛋白高变区的氨基酸序列。使用针对FCV的多克隆抗血清通过蛋白质免疫印迹分析表明,所有分离株的衣壳蛋白具有高度交叉反应性。采用逆转录聚合酶链反应获得FCV衣壳蛋白高变E区的序列信息。在FCV衣壳蛋白E区的426至458位氨基酸之间发生了氨基酸替换。基于该序列信息的序列数据和系统发育重建与通过双向交叉中和确定的分离株之间的抗原差异高度相关。这些结果与之前使用FCV不同分离株的报道一致,即氨基酸差异与血清学相关。这进一步支持了以下假设:从426至458位氨基酸的FCV衣壳蛋白E区包含对FCV抗原变异很重要的血清型决定簇。

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