Prados F J, Viñuela E, Alcamí A
Centro de Biología Molecular, Facultad de Ciencias, Universidad Autónoma, Madrid, Spain.
J Virol. 1993 May;67(5):2475-85. doi: 10.1128/JVI.67.5.2475-2485.1993.
The gene encoding protein p32, the most abundant and immunogenic protein induced by African swine fever virus at early times of infection, has been mapped in the EcoRI C' fragment of the genome of the Vero cell-adapted virus strain BA71V. Sequencing analysis has shown the existence of an open reading frame, named C'204L, encoding 204 amino acids. The protein is phosphorylated in serine residues located in the 115 N-terminal amino acids and was phosphorylated when expressed in cells infected with a vaccinia virus recombinant. Protein p32 is not glycosylated in spite of the presence of two putative N-glycosylation sites in the deduced amino acid sequence of the polypeptide. Immunofluorescence experiments have shown that the protein is localized in the cytoplasm of infected cells and not in the plasma membrane. In addition, the protein has been found in the soluble fraction and not in microsomes from BA71V-infected Vero cells. Low levels of the protein have been detected in the medium from infected swine macrophages, which probably corresponds to nonspecific release of cytoplasmic proteins. The protein encoded by other virus isolates shows different electrophoretic mobilities, indicating variability of p32.
编码蛋白p32的基因,是非洲猪瘟病毒在感染早期诱导产生的最丰富且具有免疫原性的蛋白,已定位在Vero细胞适应病毒株BA71V基因组的EcoRI C'片段中。测序分析表明存在一个名为C'204L的开放阅读框,编码204个氨基酸。该蛋白在位于N端115个氨基酸的丝氨酸残基处被磷酸化,并且在痘苗病毒重组体感染的细胞中表达时也被磷酸化。尽管在该多肽的推导氨基酸序列中存在两个假定的N-糖基化位点,但蛋白p32并未被糖基化。免疫荧光实验表明该蛋白定位于受感染细胞的细胞质中,而非质膜中。此外,在BA71V感染的Vero细胞的可溶性组分中发现了该蛋白,而在微粒体中未发现。在受感染猪巨噬细胞的培养基中检测到低水平的该蛋白,这可能对应于细胞质蛋白的非特异性释放。其他病毒分离株编码的蛋白显示出不同的电泳迁移率,表明p32具有变异性。