Duverlie G, Khorsi H, Castelain S, Jaillon O, Izopet J, Lunel F, Eb F, Penin F, Wychowski C
Virologie, CHU-Hôpital Sud, Amiens, France.
J Gen Virol. 1998 Jun;79 ( Pt 6):1373-81. doi: 10.1099/0022-1317-79-6-1373.
Japanese studies have defined the discrete 2209-2248 amino acid region of the non-structural 5A protein (NS5A(2209-2248)) of hepatitis C virus genotype 1b (HCV 1b) isolates as the interferon sensitivity determining region (ISDR). European studies did not confirm these results since most of the ISDR sequences harboured an intermediate profile. Recently, a direct interaction between the NS5A protein, involving the ISDR, and the interferon-induced protein kinase (PKR) has been reported and presented as a possible explanation of HCV interferon resistance. In the present study, the entire NS5A amino acid sequence from 11 resistant and eight sensitive strains from European HCV 1b isolates was inferred from direct sequencing. The previously described important amino acid stretches and positions in NS5A were compared between the resistant and sensitive groups. Although some variations were observed, no clear differences could be directly correlated with the interferon sensitivity. However, sensitive strains were different, owing to more amino acid changes when compared to a consensus sequence from all strains. The carboxy-terminal region and especially the previously reported NS5A/V3 region showed most of the variations. Moreover, the conformational analysis of NS5A by secondary structure prediction allowed the differentiation of most sensitive strains from resistant ones. It was concluded that other regions different from ISDR were involved in resistance to interferon maybe via the interaction between NS5A and PKR.
日本的研究已将丙型肝炎病毒1b型(HCV 1b)分离株非结构5A蛋白(NS5A(2209 - 2248))中2209 - 2248个氨基酸的离散区域定义为干扰素敏感性决定区域(ISDR)。欧洲的研究并未证实这些结果,因为大多数ISDR序列呈现出中间特征。最近,有报道称NS5A蛋白(涉及ISDR)与干扰素诱导蛋白激酶(PKR)之间存在直接相互作用,并将此作为HCV对干扰素耐药的一种可能解释。在本研究中,通过直接测序推断出欧洲HCV 1b分离株中11株耐药株和8株敏感株的整个NS5A氨基酸序列。比较了耐药组和敏感组之间NS5A中先前描述的重要氨基酸片段和位置。尽管观察到了一些差异,但没有明确的差异能直接与干扰素敏感性相关。然而,敏感株有所不同,因为与所有菌株的共有序列相比,其氨基酸变化更多。羧基末端区域,尤其是先前报道的NS5A/V3区域显示出大部分变异。此外,通过二级结构预测对NS5A进行构象分析,能够区分大多数敏感株和耐药株。得出的结论是,不同于ISDR的其他区域可能通过NS5A与PKR之间的相互作用参与了对干扰素的耐药。