首页> 外文OA文献 >Comparison of full-length sequences of interferon-sensitive and resistant hepatitis C virus 1b. Sensitivity to interferon is conferred by amino acid substitutions in the NS5A region.
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Comparison of full-length sequences of interferon-sensitive and resistant hepatitis C virus 1b. Sensitivity to interferon is conferred by amino acid substitutions in the NS5A region.

机译:干扰素敏感性和抗性丙型肝炎病毒1b全长序列的比较。 NS5A区的氨基酸取代赋予了对干扰素的敏感性。

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摘要

We have previously demonstrated that sensitivity to interferon is different among hepatitis C virus (HCV) quasispecies simultaneously detected in same individuals and that interferon-resistant HCV quasispecies are selected during the treatment. To determine the genetic basis of their resistance to interferon, HCV genotype-1b was obtained from serum of three patients before and during interferon therapy, and their full-length nucleotide and deduced amino acid sequences were determined. Comparison of the pairs of interferon-resistant and interferon-sensitive HCV isolates in respective individuals demonstrated clusters of amino acid differences in the COOH-terminal half of the NS5A region (codon 2154-2383), which contained a common unique amino acid difference at codon 2218. Additional sequence data of the COOH-terminal half of the NS5A region obtained from six interferon-resistant and nine interferon-sensitive HCV confirmed the exclusive existence of missense mutations in a 40 amino acid stretch of the NS5A region around codon 2218 (from codon 2209 to 2248) in interferon-sensitive HCV. On the other hand, this region of interferon-resistant HCV was identical to that of prototype HCV genotype-1b (HCV-J, HCV-JTa, or HC-J4). We designated this region as the interferon sensitivity determining region. Thus, HCV genotype-1b with the prototype interferon sensitivity determining region appears to be interferon-resistant strains. The specific nature of these mutations might make it possible to predict prognostic effects of interferon treatment.
机译:我们先前已经证明,在同一个体中同时检测到的丙型肝炎病毒(HCV)准种对干扰素的敏感性不同,并且在治疗期间选择了抗干扰素的HCV准种。为了确定其抗干扰素的遗传基础,从三名患者在干扰素治疗之前和期间的血清中获得了HCV基因型1b,并确定了其全长核苷酸和推导的氨基酸序列。在各个个体中对干扰素抗性和干扰素敏感性HCV分离株对的比较表明,在NS5A区COOH末端一半(密码子2154-2383)中存在氨基酸差异簇,该密码子在密码子上包含常见的独特氨基酸差异2218.从六个干扰素抗性和九个干扰素敏感的HCV获得的NS5A区COOH末端一半的其他序列数据证实,密码子2218周围NS5A区的40个氨基酸段中存在错义突变(来自密码子) 2209至2248)。另一方面,该抗干扰素HCV区域与原型HCV基因型-1b(HCV-J,HCV-JTa或HC-J4)相同。我们将该区域指定为干扰素敏感性确定区域。因此,具有原型干扰素敏感性确定区域的HCV基因型-1b似乎是抗干扰素菌株。这些突变的特殊性质可能使预测干扰素治疗的预后效果成为可能。

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