Takayama M, Oya A
Microbiol Immunol. 1985;29(7):635-43. doi: 10.1111/j.1348-0421.1985.tb00867.x.
The formation of varicella-zoster (V-Z) virus-associated antigens was studied in V-Z virus-infected Vero cells by means of indirect immunofluorescence. Early antigen (EA) was first detected inside V-Z virus-infected Vero cells 4 to 6 hr after infection, whereas surface membrane antigen (SMA) was expressed on the outer surface of infected cells 2 to 3 hr later than EA, and intranuclear late antigen (LA) was detected several hours later than SMA antigen. EA expression was not inhibited by cytosine arabinoside (Ara-C) treatment, whereas LA formation was completely blocked by Ara-C. The presence of two components of SMA early SMA (ESMA) and late SMA (LSMA), was suggested by this difference in susceptibility to Ara-C. The formation of all viral antigens, EA, SMA, and LA, was blocked by inhibitors of RNA and protein synthesis.
通过间接免疫荧光法,研究了水痘 - 带状疱疹(V - Z)病毒感染的非洲绿猴肾(Vero)细胞中V - Z病毒相关抗原的形成。感染后4至6小时,在V - Z病毒感染的Vero细胞内首次检测到早期抗原(EA),而表面膜抗原(SMA)在感染细胞外表面的表达比EA晚2至3小时,核内晚期抗原(LA)的检测比SMA抗原晚数小时。阿糖胞苷(Ara - C)处理不抑制EA的表达,而LA的形成则被Ara - C完全阻断。对Ara - C敏感性的这种差异提示存在早期SMA(ESMA)和晚期SMA(LSMA)两种SMA成分。RNA和蛋白质合成抑制剂可阻断所有病毒抗原EA、SMA和LA的形成。