Zou S, Chaudhary R K
Laboratory for Viral Hepatitis, Laboratory Centre for Disease Control, Health and Welfare, Ottawa, Ontario, Canada.
Res Virol. 1991 Sep-Oct;142(5):381-5. doi: 10.1016/0923-2516(91)90005-n.
The kinetics of replication of hepatitis A virus (LCDC-01) was studied in foetal rhesus monkey kidney cells (FRhK-4). Cells infected at a multiplicity of infection (MOI) of 2.0 showed no viral antigen production until 12 h post-infection using radioimmuno assay (RIA); however, at 48 h post-infection a logarithmic increase in antigen concentration began, which peaked by day 7. Similar patterns were observed with cultures infected with lower MOI (0.20 and 0.02) but events were delayed by about 24 h. In contrast, detection of antigen by fluorescence antibody methods occurred at only 72 h after inoculation, with either 2.0 or 0.02 MOI, and peaked by day 9. The production of infectious virus did not begin until 24 h post-infection as measured by RIA and gradually peaked by day 6. Viral RNA was first detected 24 h post-infection by hybridization assay. The amount of viral RNA in the infected cells increased significantly between days 4 to 7. Restriction in the synthesis of RNA or infectious virus was not observed.
在恒河猴胎儿肾细胞(FRhK - 4)中研究了甲型肝炎病毒(LCDC - 01)的复制动力学。以感染复数(MOI)为2.0感染的细胞,直到感染后12小时,使用放射免疫测定法(RIA)均未检测到病毒抗原产生;然而,在感染后48小时,抗原浓度开始呈对数增加,并在第7天达到峰值。用较低MOI(0.20和0.02)感染的培养物也观察到类似模式,但事件延迟约24小时。相比之下,用荧光抗体法检测抗原在接种后72小时才出现,MOI为2.0或0.02时均如此,并在第9天达到峰值。通过RIA测定,感染性病毒直到感染后24小时才开始产生,并在第6天逐渐达到峰值。通过杂交测定在感染后24小时首次检测到病毒RNA。感染细胞中病毒RNA的量在第4至7天之间显著增加。未观察到RNA或感染性病毒合成的限制。