García J, García-Barreno B, Vivo A, Melero J A
Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Virology. 1993 Jul;195(1):243-7. doi: 10.1006/viro.1993.1366.
Immunofluorescence staining and immunoelectron microscopy of respiratory syncytial (RS) virus-infected cells revealed the presence of cytoplasmic inclusions that were specifically labeled with monoclonal antibodies directed against the nucleoprotein (NP), the phosphoprotein (P), or the 22K protein. Transient expression of these three proteins with the vaccinia-T7 system, either individually or in different combinations, demonstrated that coexpression of NP and P was sufficient to induce the formation of cytoplasmic inclusions similar to those found in RS virus-infected cells. In addition, the 22K protein was also incorporated to the inclusions when coexpressed with both NP and P proteins. Immunobinding assays revealed the presence of NP-P and NP-22K complexes in extracts of RS virus-infected cells. These complexes were also detected in extracts of transfected cells that coexpressed the corresponding proteins. The implications of these results for the RS virus replicative cycle are discussed.
对呼吸道合胞(RS)病毒感染细胞进行免疫荧光染色和免疫电子显微镜检查发现,存在胞质内含物,这些内含物被针对核蛋白(NP)、磷蛋白(P)或22K蛋白的单克隆抗体特异性标记。利用痘苗-T7系统单独或不同组合瞬时表达这三种蛋白,结果表明NP和P的共表达足以诱导形成类似于RS病毒感染细胞中发现的胞质内含物。此外,当与NP和P蛋白共表达时,22K蛋白也会掺入到内含物中。免疫结合试验显示RS病毒感染细胞提取物中存在NP-P和NP-22K复合物。在共表达相应蛋白的转染细胞提取物中也检测到了这些复合物。讨论了这些结果对RS病毒复制周期的影响。