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首页> 外文期刊>Virology >Quasispecies Heterogeneity and Constraints on the Evolution of the 5' Noncoding Region of Hepatitis C Virus (HCV): Relationship with HCV Resistance to Interferon-α Therapy
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Quasispecies Heterogeneity and Constraints on the Evolution of the 5' Noncoding Region of Hepatitis C Virus (HCV): Relationship with HCV Resistance to Interferon-α Therapy

机译:准种异质性和对丙型肝炎病毒(HCV)5'非编码区进化的限制:与HCV对干扰素-α治疗的抗性的关系

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Hepatitis C virus (HCV) polyprotein translation depends on direct internal entry of the 40S ribosomal subunit mediated by an internal ribosome entry segment (IRES) located in the 5' noncoding (5'NC) region of the viral genome. HCV is genetically heterogeneous and is characterized by the existence of a quasispecies distribution of the virus population within a single infected individual. Cloning and sequencing strategies were used to characterize 5'NC quasispecies genetically. Similar to coding regions, the HCV 5'NC region was distributed as a quasispecies, but it appeared to be subjected to stronger conservatory constraints than other regions of the HCV genome, probably due to the need for structural (and functional) conservation of the IRES. Indeed, most of the quasispecies substitutions were in unpaired regions of the IRES or clustered such that base-pairing was maintained, whereas only 21% were expected to result in a loss of base-pairing. Quasispeciesrelated structural changes could be predicted in the core cruciform of IRES domain III composed of the RNA helices which extend from the four-way junction JIIIabc, mostly in minor variants, but sometimes in major ones. The results presented here suggest the simultaneous presence in infected patients of a mixture of genetically distinct but closely related IRES sequences that may have different structures. No significant genetic changes of 5'NC quasispecies were observed after interferon-α treatment, except in patients with mixed genotype infection who cleared one of the infecting strains during therapy, suggesting that the quasispecies distribution of IRES sequences does not play a role in HCV resistance to interferon-α therapy. In contrast, the overall quasispecies distribution of HCV genomes (including IRES sequences) might participate in regulation of hepatic and extrahepatic HCV replication.
机译:丙型肝炎病毒(HCV)多蛋白翻译取决于位于病毒基因组5'非编码(5'NC)区的内部核糖体进入片段(IRES)介导的40S核糖体亚基的直接内部进入。 HCV在遗传上是异质的,其特征是单个感染个体中存在病毒种群的准种分布。克隆和测序策略被用来从遗传上表征5'NC准种。与编码区相似,HCV 5'NC区作为准种分布,但它似乎比HCV基因组的其他区受到更强的保守性约束,这可能是由于需要IRES的结构(和功能)保守。实际上,大多数准种替换都位于IRES的未配对区域中或成簇,从而维持了碱基配对,而只有21%的预期会导致碱基配对丢失。可以在IRES结构域III的核心十字形中预测准物种相关的结构变化,该结构由RNA螺旋组成,RNA螺旋从四向连接JIIIabc延伸,主要是次要变体,但有时是主要变体。此处显示的结果表明,在感染患者中同时存在可能具有不同结构的遗传上不同但密切相关的IRES序列的混合物。干扰素-α治疗后未观察到5'NC准种的显着遗传变化,除了混合基因型感染的患者在治疗过程中清除了一种感染株外,这表明IRES序列的准种分布在HCV抗性中不起作用干扰素-α疗法。相反,HCV基因组(包括IRES序列)的总体准物种分布可能参与肝和肝外HCV复制的调节。

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