Gastaminza Pablo, Kapadia Sharookh B, Chisari Francis V
The Scripps Research Institute, Maildrop SBR-1010550, North Torrey Pines Road, La Jolla, CA 92037, USA.
J Virol. 2006 Nov;80(22):11074-81. doi: 10.1128/JVI.01150-06. Epub 2006 Sep 6.
The recent development of a cell culture infection model for hepatitis C virus (HCV) permits the production of infectious particles in vitro. In this report, we demonstrate that infectious particles are present both within the infected cells and in the supernatant. Kinetic analysis indicates that intracellular particles constitute precursors of the secreted infectious virus. Ultracentrifugation analyses indicate that intracellular infectious viral particles are similar in size (approximately 65 to 70 nm) but different in buoyant density (approximately 1.15 to 1.20 g/ml) from extracellular particles (approximately 1.03 to 1.16 g/ml). These results indicate that infectious HCV particles are assembled intracellularly and that their biochemical composition is altered during viral egress.
丙型肝炎病毒(HCV)细胞培养感染模型的最新进展使得在体外能够产生感染性颗粒。在本报告中,我们证明感染性颗粒既存在于受感染细胞内,也存在于上清液中。动力学分析表明,细胞内颗粒构成分泌型感染性病毒的前体。超速离心分析表明,细胞内感染性病毒颗粒的大小(约65至70纳米)与细胞外颗粒(约1.03至1.16克/毫升)相似,但浮力密度不同(约1.15至1.20克/毫升)。这些结果表明,感染性HCV颗粒在细胞内组装,并且其生化组成在病毒释放过程中发生改变。