Suppr超能文献

丙型肝炎病毒5'非编码区的序列变异性:一种新病毒类型的鉴定及序列多样性的限制

Sequence variability in the 5' non-coding region of hepatitis C virus: identification of a new virus type and restrictions on sequence diversity.

作者信息

Simmonds P, McOmish F, Yap P L, Chan S W, Lin C K, Dusheiko G, Saeed A A, Holmes E C

机构信息

Department of Medical Microbiology, Medical School, University of Edinburgh, U.K.

出版信息

J Gen Virol. 1993 Apr;74 ( Pt 4):661-8. doi: 10.1099/0022-1317-74-4-661.

Abstract

We have analysed the pattern of nucleotide sequence variability in the 5' non-coding region (5' NCR) of geographically dispersed variants of hepatitis C virus (HCV). Phylogenetic analysis of sequences in this region indicated the existence of a new virus type, provisionally termed type 4, the identity of which was confirmed by further analysis of the more variable part of the HCV core protein coding region. The geographical distribution of HCV type 4 was distinct from that of other HCV types, it being particularly widespread in Africa and absent or rare in Europe and the Far East. Much of the variability in the 5' NCR appears to be constrained by a requirement for specific secondary structures in the viral RNA. In one of the most variable regions of the 5' NCR (positions -169 to -114), most of the nucleotide changes that are characteristic of different HCV types were covariant, with complementary substitutions at other positions. According to the proposed secondary structure of the 5' NCR, such changes preserved base pairing within a stem-loop structure, whereas the nucleotide insertions found in a proportion of 5' NCR sequences, including those of type 4, localized exclusively to the non-base-paired terminal loop. The specific nucleotide substitutions in the 5' NCR that differentiate each of the four HCV types can be detected by restriction enzyme cleavage, providing a rapid and reliable method for virus typing.

摘要

我们分析了丙型肝炎病毒(HCV)地理分布变异株5'非编码区(5'NCR)的核苷酸序列变异性模式。该区域序列的系统发育分析表明存在一种新的病毒类型,暂称为4型,通过对HCV核心蛋白编码区更多可变部分的进一步分析证实了其身份。HCV 4型的地理分布与其他HCV类型不同,它在非洲特别普遍,在欧洲和远东地区不存在或罕见。5'NCR中的许多变异性似乎受到病毒RNA特定二级结构要求的限制。在5'NCR最可变的区域之一(位置-169至-114),不同HCV类型特有的大多数核苷酸变化是协变的,在其他位置有互补取代。根据5'NCR的二级结构推测,这些变化保留了茎环结构内的碱基配对,而在一部分5'NCR序列(包括4型序列)中发现的核苷酸插入仅局限于非碱基配对的末端环。通过限制性酶切可以检测到区分四种HCV类型的5'NCR中的特定核苷酸取代,这为病毒分型提供了一种快速可靠的方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验