Manzin A, Solforosi L, Petrelli E, Macarri G, Tosone G, Piazza M, Clementi M
Istituto di Microbiologia, Università di Ancona, Ancona, Italy.
J Virol. 1998 Jul;72(7):6271-6. doi: 10.1128/JVI.72.7.6271-6276.1998.
The hypervariable region 1 (HVR-1) of the putative envelope encoding E2 region of hepatitis C virus (HCV) RNA was analyzed in sequential samples from three patients with acute type C hepatitis infected from different sources to address (i) the dynamics of intrahost HCV variability during the primary infection and (ii) the role of host selective pressure in driving viral genetic evolution. HVR-1 sequences from 20 clones per each point in time were analyzed after amplification, cloning, and purification of plasmid DNA from single colonies of transformed cells. The intrasample evolutionary analysis (nonsynonymous mutations per nonsynonymous site [Ka], synonymous mutations per synonymous site [Ks], Ka/Ks ratio, and genetic distances [gd]) documented low gd in early samples (ranging from 2. 11 to 7.79%) and a further decrease after seroconversion (from 0 to 4.80%), suggesting that primary HCV infection is an oligoclonal event, and found different levels and dynamics of host pressure in the three cases. The intersample analysis (pairwise comparisons of intrapatient sequences; rKa, rKs, rKa/rKs ratio, and gd) confirmed the individual features of HCV genetic evolution in the three subjects and pointed to the relative contribution of either neutral evolution or selective forces in driving viral variability, documenting that adaptation of HCV for persistence in vivo follows different routes, probably representing the molecular counterpart of the viral fitness for individual environments.
对来自三名不同来源感染的急性丙型肝炎患者的连续样本,分析了丙型肝炎病毒(HCV)RNA推定包膜编码E2区的高变区1(HVR-1),以探讨:(i)初次感染期间宿主内HCV变异性的动态变化;(ii)宿主选择压力在驱动病毒基因进化中的作用。从转化细胞的单菌落中扩增、克隆和纯化质粒DNA后,对每个时间点的20个克隆的HVR-1序列进行分析。样本内进化分析(每个非同义位点的非同义突变数[Ka]、每个同义位点的同义突变数[Ks]、Ka/Ks比值和遗传距离[gd])显示早期样本中gd较低(范围为2.11%至7.79%),血清转化后进一步降低(从0至4.80%),这表明初次HCV感染是一个寡克隆事件,并发现三例患者中宿主压力的水平和动态变化不同。样本间分析(患者内序列的成对比较;rKa、rKs、rKa/rKs比值和gd)证实了三名受试者中HCV基因进化的个体特征,并指出了中性进化或选择力在驱动病毒变异性方面的相对贡献,证明HCV在体内持续存在的适应性遵循不同途径,这可能代表了病毒在个体环境中适应性的分子对应物。