Goens S D, Botero S, Zemla A, Zhou C Ecale, Perdue M L
Environmental Microbial Safety Laboratory, Animal and Natural Resources Institute, Beltsville Agriculture Research Center, Agricultural Research Service, United States Department of Agriculture, 10300 Baltimore Avenue, Building 173, BARC-East, Beltsville, MD 20705, USA.
Bioinformatics, Chemical and Biological National Security Program, Computing Applications and Research Department, Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, CA 94550, USA.
J Gen Virol. 2004 Nov;85(Pt 11):3195-3203. doi: 10.1099/vir.0.80159-0.
Bovine enteroviruses are members of the family Picornaviridae, genus Enterovirus. Whilst little is known about their pathogenic potential, they are apparently endemic in some cattle and cattle environments. Only one of the two current serotypes has been sequenced completely. In this report, the entire genome sequences of bovine enterovirus 2 (BEV-2) strain PS87 and a recent isolate from an endemically infected herd in Maryland, USA (Wye3A) are presented. The recent isolate clearly segregated phylogenetically with sequences representing the BEV-2 serotype, as did other isolates from the endemic herd. The Wye3A isolate shared 82 % nucleotide sequence identity with the PS87 strain and 68 % identity with a BEV-1 strain (VG5-27). Comparison of BEV-2 and BEV-1 deduced protein sequences revealed 72-73 % identity and showed that most differences were single amino acid changes or single deletions, with the exception of the VP1 protein, where both BEV-2 sequences were 7 aa shorter than that of BEV-1. Homology modelling of the capsid proteins of BEV-2 against protein database entries for picornaviruses indicated six significant differences among bovine enteroviruses and other members of the family Picornaviridae. Five of these were on the 'rim' of the proposed enterovirus receptor-binding site or 'canyon' (VP1) and one was near the base of the canyon (VP3). Two of these regions varied enough to distinguish BEV-2 from BEV-1 strains. This is the first report and analysis of full-length sequences for BEV-2. Continued analysis of these wild-type strains should yield useful information for genotyping enteroviruses and modelling enterovirus capsid structure.
牛肠道病毒是小RNA病毒科肠道病毒属的成员。虽然对它们的致病潜力了解甚少,但它们显然在一些牛群和牛的生存环境中呈地方性流行。目前的两种血清型中只有一种已被完全测序。在本报告中,展示了牛肠道病毒2(BEV-2)PS87株以及最近从美国马里兰州一个地方性感染牛群中分离出的毒株(Wye3A)的全基因组序列。最近分离出的毒株在系统发育上与代表BEV-2血清型的序列明显分开,来自地方性流行牛群的其他分离株也是如此。Wye3A分离株与PS87株的核苷酸序列同一性为82%,与BEV-1株(VG5-27)的同一性为68%。BEV-2和BEV-1推导的蛋白质序列比较显示同一性为72 - 73%,并且表明大多数差异是单个氨基酸变化或单个缺失,但VP1蛋白除外,BEV-2的两个序列都比BEV-1的短7个氨基酸。针对小RNA病毒的蛋白质数据库条目对BEV-2衣壳蛋白进行同源性建模表明,牛肠道病毒与小RNA病毒科的其他成员之间存在六个显著差异。其中五个位于拟肠道病毒受体结合位点或“峡谷”(VP1)的“边缘”,一个位于峡谷底部附近(VP3)。这些区域中的两个差异足够大,足以将BEV-2与BEV-1毒株区分开来。这是关于BEV-2全长序列的首次报告和分析。对这些野生型毒株的持续分析应该会为肠道病毒基因分型和肠道病毒衣壳结构建模提供有用信息。