Liu Xinsheng, Oka Tomoichiro, Wang Qiuhong
Food Animal Health Research Program, Ohio Agricultural Research and Development Center, College of Food, Agricultural and Environmental Sciences, Department of Veterinary Preventive Medicine, The Ohio State University, Wooster, OH, USA,
Arch Microbiol. 2015 Oct;197(8):1033-40. doi: 10.1007/s00203-015-1139-7. Epub 2015 Aug 28.
Porcine kobuvirus has been detected from pig fecal samples in the USA, but there is still no information on the full-length genomes. In this study, we characterized the first complete genomic sequence of a US porcine kobuvirus strain OH/RV50/2011. The viral genome is 8123 nucleotides (nt) long, including a 576-nt 5'-untranslated region (UTR), a 7380-nt polyprotein encoding sequence, and a 167-nt 3'-UTR. A complete genome sequence alignment suggested that two types of porcine kobuviruses were found based on whether a 30-aa deletion existed in the 2B encoding region. Furthermore, several conserved motifs that can be used for the design of universal kobuvirus or porcine kobuvirus-specific primers were verified in non-structural protein genes. Phylogenetic analysis based on the complete genome sequence showed that RV50 was grouped with other porcine kobuviruses and more closely related to Chinese strains. Secondary structure analysis of the 5'-UTR showed that RV50 has three stem-loop domains in the first 108 nt and has a potential hepacivirus-/pestivirus-like type IV group-B-like internal ribosomal entry site, like the porcine kobuvirus prototype strain S-1. Codon usage analysis showed that the most preferred usage tends to be C or U at the end of a codon in a porcine kobuvirus genome. These results will be useful in understanding the evolution of porcine kobuviruses .
在美国的猪粪便样本中已检测到猪杯状病毒,但关于其全长基因组仍无相关信息。在本研究中,我们对美国猪杯状病毒毒株OH/RV50/2011的首个完整基因组序列进行了特征分析。该病毒基因组长度为8123个核苷酸(nt),包括一个576 nt的5'非翻译区(UTR)、一个7380 nt的多聚蛋白编码序列和一个167 nt的3'UTR。完整基因组序列比对表明,根据2B编码区是否存在30个氨基酸的缺失,可发现两种类型的猪杯状病毒。此外,在非结构蛋白基因中验证了几个可用于设计通用杯状病毒或猪杯状病毒特异性引物的保守基序。基于完整基因组序列的系统发育分析表明,RV50与其他猪杯状病毒归为一组,且与中国毒株关系更为密切。5'UTR的二级结构分析表明,RV50在前108 nt中有三个茎环结构域,并且具有潜在的丙型肝炎病毒/瘟病毒样IV型B组样内部核糖体进入位点,类似于猪杯状病毒原型毒株S-1。密码子使用分析表明,猪杯状病毒基因组中密码子最偏好的使用倾向于在密码子末端为C或U。这些结果将有助于理解猪杯状病毒的进化。