Department of Microbiology and Immunology, Tulane University Health Sciences Center, New Orleans, LA, USA.
Virology. 2010 Nov 10;407(1):110-9. doi: 10.1016/j.virol.2010.07.026. Epub 2010 Aug 25.
To gain a more complete understanding of hepatitis C virus (HCV) entry, we initially assessed the rate at which HCV initiates productive attachment/infection in vitro and discovered it to be slower than most viruses. Since HCV, including cell culture-derived HCV (HCVcc), exhibits a broad-density profile (1.01-1.16 g/ml), we hypothesized that the varying densities of the HCVcc particles present in the inoculum may be responsible for this prolonged entry phenotype. To test this hypothesis, we show that during infection, particles of high density disappeared from the viral inoculum sooner and initiated productive infection faster than virions of low density. Moreover, we could alter the rate of attachment/infection initiation by increasing or decreasing the density of the cell culture medium. Together, these findings demonstrate that the relationship between the density of HCVcc and the density of the extracellular milieu can significantly impact the rate at which HCVcc productively interacts with target cells in vitro.
为了更全面地了解丙型肝炎病毒(HCV)的进入机制,我们首先评估了 HCV 在体外开始有效附着/感染的速度,结果发现其速度比大多数病毒都要慢。由于 HCV(包括细胞培养衍生的 HCV [HCVcc])表现出广泛的密度分布(1.01-1.16 g/ml),我们假设接种物中存在的 HCVcc 颗粒的不同密度可能是导致这种延长进入表型的原因。为了验证这一假设,我们表明在感染过程中,高密度的颗粒从病毒接种物中更快地消失,并比低密度的病毒粒子更快地启动有效的感染。此外,我们可以通过增加或降低细胞培养液的密度来改变附着/感染起始的速度。总之,这些发现表明 HCVcc 的密度与细胞外环境的密度之间的关系可以显著影响 HCVcc 与体外靶细胞有效相互作用的速度。