Kanazawa Y, Hayashi N, Mita E, Li T, Hagiwara H, Kasahara A, Fusamoto H, Kamada T
First Department of Medicine, Osaka University School of Medicine, Japan.
Hepatology. 1994 Nov;20(5):1121-30.
The quasispecies nature of hepatitis C virus genome distribution is most evident in hypervariable regions of the putative envelope 2 domain. Eight patients with chronic hepatitis C treated with interferon-alpha were studied as to heterogeneity of the hypervariable regions to clarify the implications of quasispecies. More than 10 recombinant clones generated from polymerase chain reaction-amplified products of the hypervariable regions were sequenced. The sets of clones derived from long-term responders before interferon therapy showed a significantly lower (p < 0.05) degree of sequence complexity of the hypervariable region 1 quasispecies than those from short-term ones or non-responders. The values of nucleotide diversity (the average number of nucleotide differences per site between two randomly chosen sequences) in hypervariable region 1 before interferon therapy were also significantly lower (p < 0.05) for long-term responders (mean, 2.31 x 10(-2)). In some cases, nucleotide diversity decreased remarkably during interferon therapy, whereas the values remained unchanged in other cases. In one interesting case, a short-term response was first noted with the nucleotide diversity decreasing from 13.98 x 10(-2) to 0.21 x 10(-2); namely, the diversity of the quasispecies was significantly reduced, and then a long-term response was observed after an additional course of interferon therapy. Thus, the degree of quasispecies' complexity and diversity of hypervariable region 1 was closely correlated with the responsiveness to interferon therapy in chronic hepatitis C patients, and thus may have some influence on interferon efficacy.
丙型肝炎病毒基因组分布的准种特性在假定的包膜2结构域的高变区最为明显。对8例接受α干扰素治疗的慢性丙型肝炎患者的高变区异质性进行了研究,以阐明准种的意义。对从高变区的聚合酶链反应扩增产物产生的10多个重组克隆进行了测序。干扰素治疗前长期应答者衍生的克隆组显示,高变区1准种的序列复杂性程度明显低于短期应答者或无应答者(p<0.05)。干扰素治疗前高变区1的核苷酸多样性值(两个随机选择序列之间每个位点的核苷酸差异平均数)在长期应答者中也明显较低(p<0.05)(平均值,2.31×10^(-2))。在某些情况下,干扰素治疗期间核苷酸多样性显著降低,而在其他情况下该值保持不变。在一个有趣的病例中,首先观察到短期应答,核苷酸多样性从13.98×10^(-2)降至0.21×10^(-2);即准种的多样性显著降低,然后在额外疗程的干扰素治疗后观察到长期应答。因此,高变区1准种的复杂性和多样性程度与慢性丙型肝炎患者对干扰素治疗的反应性密切相关,因此可能对干扰素疗效有一定影响。