Bishop N E
Hepatitis Research Unit, Macfarlane Burnet Centre for Medical Research, Fairfield, Vict., Australia.
Intervirology. 2000;43(1):36-47. doi: 10.1159/000025021.
Dense, RNase-sensitive, VP2-containing, non-infectious hepatitis A virus (HAV) particles were found to be formed at early times after the infection of cultured cells. These particles formed with kinetics mirroring those reported for HAV uncoating. The kinetics of the formation of dense HAV particles corresponded to a decrease in detectable, mature input virions, as detected by RNA dot blot hybridization of CsCl density gradient fractions. The dense HAV particles did not appear to have altered sedimentation coefficients, and as the fate of small capsid protein VP4 is not yet known, these particles cannot yet be termed 'A particles' or 'infectosomes', as have the uncoating intermediates in some picornavirus-cell systems.
在培养细胞感染后的早期发现形成了致密的、对核糖核酸酶敏感的、含VP2的非感染性甲型肝炎病毒(HAV)颗粒。这些颗粒形成的动力学反映了报道的HAV脱壳的动力学。通过CsCl密度梯度分级分离物的RNA斑点印迹杂交检测,致密HAV颗粒形成的动力学与可检测到的成熟输入病毒粒子的减少相对应。致密HAV颗粒的沉降系数似乎没有改变,并且由于小衣壳蛋白VP4的命运尚不清楚,这些颗粒还不能像一些小RNA病毒-细胞系统中的脱壳中间体那样被称为“A颗粒”或“感染体”。