Giangaspero Massimo, Harasawa Ryô
Veterinary Microbiology, School of Veterinary Medicine, Faculty of Agriculture, Iwate University, 18-8 Ueda 3 Chome, Morioka 020-8550, Iwate, Japan.
J Virol Methods. 2007 Dec;146(1-2):375-88. doi: 10.1016/j.jviromet.2007.07.009. Epub 2007 Aug 23.
The palindromic nucleotide substitutions (PNS) at the three variable loci (V1, V2 and V3) in the 5' untranslated region (UTR) of Pestivirus RNA have been considered for taxonomical segregation of species, through the evaluation of 430 genomic sequences. On the basis of qualitative and quantitative secondary structure characteristics, six species have been identified: Bovine viral diarrhea virus 1 (BVDV-1), Bovine viral diarrhea virus 2 (BVDV-2), Classical swine fever virus (CSFV), Border disease virus (BDV), the tentative species Giraffe and a new proposed taxon named Pronghorn. The first step was qualitative and consisted in the characterization of the different positions of the three stems and loops in the 5' UTR sequences of all the strains under consideration belonging to the genus. Secondary structure sequences showing divergent base-pair combinations have been aligned for comparison. Palindromic positions have been characterized according to changes in nucleotide base-pairs identifying low-variable positions (LVP) including base-pairs present in less than 80% of the genus. The second step was quantitative, allowing the identification of genomic groups by clustering the base-pair combinations according to LVP. Relatedness among types was evaluated to identify homogeneous groups. Cross comparisons between types within the genus have been evaluated by computing the divergence percentage thus clarifying borderline and multirelated sequences.
通过对430个基因组序列的评估,瘟病毒RNA 5'非翻译区(UTR)中三个可变位点(V1、V2和V3)的回文核苷酸替换(PNS)已被用于物种的分类隔离。基于定性和定量的二级结构特征,已鉴定出六个物种:牛病毒性腹泻病毒1型(BVDV-1)、牛病毒性腹泻病毒2型(BVDV-2)、经典猪瘟病毒(CSFV)、边界病病毒(BDV)、暂定物种长颈鹿以及一个新提议的分类单元叉角羚。第一步是定性的,包括对所考虑的属于该属的所有菌株5'UTR序列中三个茎环的不同位置进行特征描述。已对显示不同碱基对组合的二级结构序列进行比对以作比较。已根据核苷酸碱基对的变化对回文位置进行特征描述,确定低可变位置(LVP),包括在该属中出现频率低于80%的碱基对。第二步是定量的,通过根据LVP对碱基对组合进行聚类来鉴定基因组群。评估各类型之间的相关性以识别同质群。通过计算分歧百分比评估该属内各类型之间的交叉比较,从而阐明边界序列和多相关序列。