Robbins S J, Rapp F
Arch Virol. 1982;71(1):85-91. doi: 10.1007/BF01315178.
Synthesis of virus-specific proteins in a persistent, nonproductive paramyxovirus infection derived from the peripheral blood leukocytes of a patient with subacute sclerosing panencephalitis (SSPE) was investigated. The persistently infected cells expressed cytoplasmic virus-specific antigens and generated paramyxovirus nucleocapsids throughout long-term passage. When analyzed by specific immunoprecipitation and sodium dodecyl sulfate-polyacrylamide gel electrophoresis, most of the virus structural proteins were synthesized in acutely infected cells, but only three of the proteins could be readily detected in persistently infected cells. The two structural proteins whose synthesis was most clearly restricted had molecular weights of 69,000 and 41,000 daltons and represented the putative HN and M virus proteins. The similarities between the restriction of virus protein synthesis in this system and that reported previously for other persistent paramyxovirus infections derived from SSPE suggest that a common mechanism may be involved in the maintenance of such infections.
对源自亚急性硬化性全脑炎(SSPE)患者外周血白细胞的持续性、非增殖性副粘病毒感染中病毒特异性蛋白的合成进行了研究。持续感染的细胞表达细胞质病毒特异性抗原,并在长期传代过程中产生副粘病毒核衣壳。通过特异性免疫沉淀和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析,大多数病毒结构蛋白在急性感染细胞中合成,但在持续感染细胞中只能轻易检测到其中三种蛋白。合成最明显受限的两种结构蛋白分子量分别为69,000和41,000道尔顿,分别代表假定的HN和M病毒蛋白。该系统中病毒蛋白合成的限制与先前报道的源自SSPE的其他持续性副粘病毒感染的限制之间的相似性表明,维持此类感染可能涉及共同机制。