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火鸡源呼肠孤病毒S1基因组片段的序列及系统发育分析

Sequence and phylogenetic analysis of the S1 genome segment of turkey-origin reoviruses.

作者信息

Day J Michael, Pantin-Jackwood Mary J, Spackman Erica

机构信息

Southeast Poultry Research Laboratory, USDA-ARS, 934 College Station Road, Athens, GA 30605, USA.

出版信息

Virus Genes. 2007 Oct;35(2):235-42. doi: 10.1007/s11262-006-0044-1. Epub 2007 Jan 30.

DOI:10.1007/s11262-006-0044-1
PMID:17265142
Abstract

Based on previous reports characterizing the turkey-origin avian reovirus (TRV) sigmaB (sigma2) major outer capsid protein gene, the TRVs may represent a new group within the fusogenic orthoreoviruses. However, no sequence data from other TRV genes or genome segments has been reported. The sigmaC protein encoded by the avian reovirus S1 genome segment is the cell attachment protein and a major antigenic determinant for avian reovirus. The chicken reovirus S1 genome segment is well characterized and is well conserved in viruses from that species. This report details the amplification, cloning and sequencing of the entire S1 genome segment from two and the entire coding sequences of the sigmaC, p10 and p17 genes from an additional five TRVs. Sequence analysis reveals that of the three proteins encoded by the TRV S1 genome segment, sigmaC shares at most 57% amino acid identity with sigmaC from the chicken reovirus reference strain S1133, while the most similar p10 and p17 proteins share 72% and 61% identity, respectively, with the corresponding S1133 proteins. The most closely related mammalian reovirus, the fusogenic Nelson Bay reovirus, encodes a sigmaC protein that shares from 25% to 28% amino acid identity with the TRV sigmaC proteins. This report supports the earlier suggestion that the TRVs are a separate virus species within the Orthoreovirus genus, and may provide some insight into TRV host specificity and pathogenesis.

摘要

基于之前对源自火鸡的禽呼肠孤病毒(TRV)σB(σ2)主要外衣壳蛋白基因的报道,TRV可能代表融合性正呼肠孤病毒中的一个新组。然而,尚未有来自其他TRV基因或基因组片段的序列数据报道。禽呼肠孤病毒S1基因组片段编码的σC蛋白是细胞附着蛋白,也是禽呼肠孤病毒的主要抗原决定簇。鸡呼肠孤病毒S1基因组片段已得到充分表征,并且在该物种的病毒中高度保守。本报告详细描述了从另外两个TRV中扩增、克隆和测序整个S1基因组片段,以及从另外五个TRV中扩增、克隆和测序σC、p10和p17基因的完整编码序列。序列分析表明,在TRV S1基因组片段编码的三种蛋白质中,σC与鸡呼肠孤病毒参考毒株S1133的σC最多有57%的氨基酸同一性,而最相似的p10和p17蛋白与相应的S1133蛋白分别有72%和61%的同一性。与TRV关系最密切的哺乳动物呼肠孤病毒,即融合性纳尔逊湾呼肠孤病毒,编码的σC蛋白与TRV的σC蛋白有25%至28%的氨基酸同一性。本报告支持了早期的观点,即TRV是正呼肠孤病毒属内一个独立的病毒种,并可能为TRV的宿主特异性和发病机制提供一些见解。

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