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1型牛病毒性腹泻病毒E2基因正向选择的证据。

Evidence for positive selection on the E2 gene of bovine viral diarrhoea virus type 1.

作者信息

Tang Fangqiang, Zhang Chuyu

机构信息

State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China.

出版信息

Virus Genes. 2007 Dec;35(3):629-34. doi: 10.1007/s11262-007-0122-z. Epub 2007 Jun 14.

DOI:10.1007/s11262-007-0122-z
PMID:17566858
Abstract

Despite the growing interest in the molecular epidemiology of pestivirus, there have been few attempts to determine which regions of the pestivirus genome are subject to positive selection, although this may be a key indicator of the nature of the interaction between host and virus. By using likelihood-based methods for phylogenetic inference, the positive selection pressure of BVDV-1 E2 gene were assessed and a site-by-site analysis of the dN/dS ratio was performed, to identify specific codons undergoing diversifying positive selection. The overall omega was 0.20, indicating that most sites were subject to strong purifying selection and five positively selected sites (886, 888, 905, 944, and 946) were identified. It is surprising to find that all the potential positively selected sites fall within the C-terminal of E2, and out of the N-terminal of E2 which is thought to be surface-exposed and therefore prime targets for host antibody response. In conclusion, these results suggest that selection favoring avoidance of antibody recognition has not been a major factor in the history of BVDV-1. Further analysis is necessary to see if amino acid substitutions in the BVDV-1 positively selected sites can lead to change of host tropism or\and escape from epitope-specific CD8 T-cell response.

摘要

尽管对瘟病毒分子流行病学的兴趣日益浓厚,但很少有人尝试确定瘟病毒基因组的哪些区域受到正选择,尽管这可能是宿主与病毒之间相互作用性质的关键指标。通过使用基于似然性的系统发育推断方法,评估了牛病毒性腹泻病毒1型(BVDV-1)E2基因的正选择压力,并对dN/dS比率进行了逐位点分析,以识别经历多样化正选择的特定密码子。总体ω值为0.20,表明大多数位点受到强烈的纯化选择,并鉴定出五个正选择位点(886、888、905、944和946)。令人惊讶的是,所有潜在的正选择位点都位于E2的C末端内,而不在被认为是表面暴露的E2的N末端内,因此是宿主抗体反应的主要靶点。总之,这些结果表明,有利于避免抗体识别的选择在BVDV-1的历史中并不是一个主要因素。有必要进一步分析BVDV-1正选择位点的氨基酸取代是否会导致宿主嗜性的改变或/和逃避表位特异性CD8 T细胞反应。

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