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人肠道病毒B型流行株的重组:结构基因组区域与非结构基因组区域的独立进化

Recombination in circulating Human enterovirus B: independent evolution of structural and non-structural genome regions.

作者信息

Lukashev Alexander N, Lashkevich Vasilii A, Ivanova Olga E, Koroleva Galina A, Hinkkanen Ari E, Ilonen Jorma

机构信息

Department of Biochemistry and Pharmacy, Åbo Akademi University, PO Box 66, 20521 Turku, Finland.

Institute of Poliomyelitis and Viral Encephalitides RAMS, Moscow, Russia.

出版信息

J Gen Virol. 2005 Dec;86(Pt 12):3281-3290. doi: 10.1099/vir.0.81264-0.

DOI:10.1099/vir.0.81264-0
PMID:16298973
Abstract

The complete nucleotide sequences of eight Human enterovirus B (HEV-B) strains were determined, representing five serotypes, E6, E7, E11, CVB3 and CVB5, which were isolated in the former Soviet Union between 1998 and 2002. All strains were mosaic recombinants and only the VP2-VP3-VP1 genome region was similar to that of the corresponding prototype HEV-B strains. In seven of the eight strains studied, the 2C-3D genome region was most similar to the prototype E30, EV74 and EV75 strains, whilst the remaining strain was most similar to the prototype E1 and E9 strains in the non-structural protein genome region. Most viruses also bore marks of additional recombination events in this part of the genome. In the 5' non-translated region, all strains were more similar to the prototype E9 than to other enteroviruses. In most cases, recombination mapped to the VP4 and 2ABC genome regions. This, together with the star-like topology of the phylogenetic trees for these genome regions, identified these genome parts as recombination hot spots. These findings further support the concept of independent evolution of enterovirus genome fragments and indicate a requirement for more advanced typing approaches. A range of available phylogenetic methods was also compared for efficient detection of recombination in enteroviruses.

摘要

测定了8株人肠道病毒B(HEV-B)毒株的完整核苷酸序列,它们代表5种血清型,即E6、E7、E11、柯萨奇病毒B3(CVB3)和柯萨奇病毒B5(CVB5),这些毒株于1998年至2002年在前苏联分离得到。所有毒株均为嵌合重组体,只有VP2-VP3-VP1基因组区域与相应的HEV-B原型毒株相似。在研究的8株毒株中的7株中,2C-3D基因组区域与原型E30、EV74和EV75毒株最为相似,而其余毒株在非结构蛋白基因组区域与原型E1和E9毒株最为相似。大多数病毒在基因组的这一部分也有额外重组事件的痕迹。在5'非翻译区,所有毒株与原型E9的相似性高于与其他肠道病毒的相似性。在大多数情况下,重组定位在VP4和2ABC基因组区域。这一点,连同这些基因组区域的系统发育树的星状拓扑结构,将这些基因组部分确定为重组热点。这些发现进一步支持了肠道病毒基因组片段独立进化的概念,并表明需要更先进的分型方法。还比较了一系列可用的系统发育方法,以有效检测肠道病毒中的重组。

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