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首页> 外文期刊>Journal of Microbiology Research >A Minireview: Molecular Understanding of HCV Infection Mechanism
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A Minireview: Molecular Understanding of HCV Infection Mechanism

机译:综述:HCV感染机制的分子理解

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摘要

Hepatitis C (HCV) is a positive polarity single-stranded (ss) RNA virus belongs to Flaviviridae family. It infects about 2% people annually throughout the world (WHO, 2012) and causes both acute and chronic hepatitis consequences permanent liver damage, hepatocellular carcinoma (HCC) and eventually death. The absence of effective means of treatment makes HCV infection a global health hazard. Due to lack of pin point of molecular mechanism, precise drug target and efficient preventive measure is still unclear. Therefore, identifying and understanding mechanistic underpinnings of viral entry, replication, assembly, and budding are crucial in owing to the development of antiviral therapy. Current host-pathogen interactions data and the infection model suggest that RNA dependent RNA polymerase activity of NS5B, along with NS5A and NS3 play central role in HCV infection mechanisms. It has been shown in numerous studies that the interactions between 5′ and 3′ UTRs (Un-translated regions) and the interactions UTRs verses host proteins play fundamental role in regulating replication and translation processes as well as their successive switching.
机译:丙型肝炎(HCV)是属于黄病毒科的正极性单链(ss)RNA病毒。它每年在全世界感染约2%的人(世卫组织,2012年),并引起急性和慢性肝炎后果,永久性肝损害,肝细胞癌(HCC)并最终导致死亡。缺乏有效的治疗手段使HCV感染成为全球健康危害。由于缺乏确切的分子机制,尚不清楚精确的药物靶向和有效的预防措施。因此,由于抗病毒治疗的发展,识别和理解病毒进入,复制,组装和出芽的机制基础至关重要。当前的宿主-病原体相互作用数据和感染模型表明,NS5B的RNA依赖性RNA聚合酶活性以及NS5A和NS3在HCV感染机制中起着核心作用。在众多研究中已经表明,5'和3'UTR(非翻译区)之间的相互作用以及UTR与宿主蛋白之间的相互作用在调节复制和翻译过程及其连续转换中起着基本作用。

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