Klevjer-Anderson P, Cheevers W P, Crawford T B
Arch Virol. 1979;60(3-4):279-89. doi: 10.1007/BF01317499.
Equine dermal fibroblasts persistently infected with equine infectious anemia virus (EIAV) show no alterations in cell morphology or growth kinetics when compared to uninfected cells. The percentage of cells immunofluorescent positive for viral proteins fluctuated, depending upon the stage of the cell cycle, while production of extracellular virus was uniform throughout the cell cycle, increasing only as the cell number increased. This was shown in log versus stationary phase cultures as well as in cultures synchronized by sterum starvation. The establishment of productive infection did not require host cell DNA synthesis. Normal levels of progeny virus were produced in cultures pretreated with mitomycin C and placed in serum-containing medium. Serum-starved cultures, however, did not support EIAV replication as well as other cultures, presumably because synthesis of provirus was inhibited.
与未感染的细胞相比,持续感染马传染性贫血病毒(EIAV)的马皮肤成纤维细胞在细胞形态或生长动力学上没有变化。病毒蛋白免疫荧光阳性细胞的百分比会波动,这取决于细胞周期的阶段,而细胞外病毒的产生在整个细胞周期中是均匀的,仅随着细胞数量的增加而增加。这在对数期与稳定期培养物中以及通过血清饥饿同步化的培养物中都得到了证实。生产性感染的建立不需要宿主细胞DNA合成。在用丝裂霉素C预处理并置于含血清培养基中的培养物中产生了正常水平的子代病毒。然而,血清饥饿的培养物不像其他培养物那样支持EIAV复制,推测是因为前病毒的合成受到了抑制。