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2型人副肠道病毒(原埃可病毒23型)的分子分析

Molecular analysis of human parechovirus type 2 (formerly echovirus 23).

作者信息

Ghazi F, Hughes P J, Hyypiä T, Stanway G

机构信息

Department of Biological Sciences, John Tabor Laboratories, University of Essex, Colchester, UK.

出版信息

J Gen Virol. 1998 Nov;79 ( Pt 11):2641-50. doi: 10.1099/0022-1317-79-11-2641.

Abstract

Picornaviruses have been divided into five genera until recently, when a sixth genus, Parechovirus, was defined. Human parechovirus type 1 (HPeV1; formerly echovirus 22) was the first recognized member of this genus and preliminary sequence analysis of echovirus 23 [now renamed human parechovirus type 2 (HPeV2)] suggested that it is also a parechovirus. Here we describe the complete nucleotide and predicted amino acid sequences of HPeV2, which indicate a close relationship to HPeV1 throughout the genome. Sequence covariance in the 5' untranslated region allows a prediction of the secondary structure, which indicates that these parechoviruses have a type 2 internal ribosome entry site, most closely related to that of cardioviruses. Overall, HPeV2 has 87.9% amino acid identity with HPeV1, most divergence being seen in regions of the capsid proteins that probably define antigenic sites. The N-terminal sequence extension to VP3, seen only in parechoviruses, is highly basic in both viruses, but has a variable sequence, suggesting that it does not have a sequence-specific role. There is an RGD motif near the C terminus of VP1, in an analogous location to that in HPeV1 which is believed to be functionally significant. The results confirm that both viruses are parechoviruses and give insights into the molecular features of this genus.

摘要

直到最近,小核糖核酸病毒一直被分为五个属,此时第六个属——细小病毒属被确定。人类1型细小病毒(HPeV1;以前称为埃可病毒22)是该属中第一个被识别的成员,对埃可病毒23(现重新命名为人类2型细小病毒,即HPeV2)的初步序列分析表明它也是一种细小病毒。在此我们描述了HPeV2的完整核苷酸序列和预测的氨基酸序列,这些序列表明其在整个基因组中与HPeV1关系密切。5'非翻译区的序列协方差使得能够预测二级结构,这表明这些细小病毒具有2型内部核糖体进入位点,与心病毒的最为密切相关。总体而言,HPeV2与HPeV1有87.9%的氨基酸同一性,在可能定义抗原位点的衣壳蛋白区域差异最大。仅在细小病毒中可见的VP3的N端序列延伸在两种病毒中都是高度碱性的,但序列可变,这表明它没有序列特异性作用。在VP1的C端附近有一个RGD基序,其位置与HPeV1中的类似,据信具有功能意义。这些结果证实这两种病毒都是细小病毒,并深入了解了该属的分子特征。

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