Bullman Susan, Kearney Karen, O'Mahony Michael, Kelly Lorraine, Whyte Paul, Fanning Seamus, Morgan John G
Department of Biological Sciences, Cork Institute of Technology, Cork, Ireland.
School of Microbiology, University College Cork, Cork, Ireland.
J Gen Virol. 2014 May;95(Pt 5):1094-1103. doi: 10.1099/vir.0.061085-0. Epub 2014 Feb 4.
A novel picornavirus from commercial broiler chickens (Gallus gallus domesticus) has been identified and genetically characterized. The viral genome consists of a single-stranded, positive-sense RNA genome of >9243 nt excluding the poly(A) tail and as such represents one of the largest picornavirus genomes reported to date. The virus genome is GC-rich with a G+C content of 54.5 %. The genomic organization is similar to other picornaviruses: 5' UTR-L-VP0-VP3-VP1-2A-2B-2C-3A-3B-3C-3D-3' UTR. The partially characterized 5' UTR of >373 nt appears to possess a type II internal ribosomal entry site (IRES), which is also found in members of the genera Aphthovirus and Cardiovirus. This IRES exhibits significant sequence similarity to turkey 'gallivirus A'. The 3' UTR of 278 nt contains the conserved 48 nt 'barbell-like' structure identified in 'passerivirus', 'gallivirus', Avihepatovirus and some Kobuvirus genus members. A predicted large open reading frame (ORF) of 8592 nt encodes a potential polyprotein precursor of 2864 amino acids. In addition, the virus contains a predicted large L protein of 462 amino acids. Pairwise sequence comparisons, along with phylogenetic analysis revealed the highest percentage identity to 'Passerivirus A' (formerly called turdivirus 1), forming a monophyletic group across the P1, P2 and P3 regions, with <40, <40 and <50 % amino acid identity respectively. Reduced identity was observed against 'gallivirus A' and members of the Kobuvirus genus. Quantitative PCR analysis estimated a range of 4×10(5) to 5×10(8) viral genome copies g(-1) in 22 (73 %) of 30 PCR-positive faeces. Based on sequence and phylogenetic analysis, we propose that this virus is the first member of a potential novel genus within the family Picornaviridae. Further studies are required to investigate the pathogenic potential of this virus within the avian host.
已鉴定出一种来自商业肉鸡(家鸡)的新型小RNA病毒,并对其进行了基因特征分析。病毒基因组由一条大于9243 nt的单链正链RNA基因组组成,不包括聚腺苷酸尾,因此是迄今为止报道的最大的小RNA病毒基因组之一。病毒基因组富含GC,G+C含量为54.5%。基因组组织与其他小RNA病毒相似:5'UTR-L-VP0-VP3-VP1-2A-2B-2C-3A-3B-3C-3D-3'UTR。部分特征化的大于373 nt的5'UTR似乎具有II型内部核糖体进入位点(IRES),在口疮病毒属和心病毒属成员中也有发现。该IRES与火鸡“鸡戊型肝炎病毒A”具有显著的序列相似性。278 nt的3'UTR包含在“雀形目病毒”、“鸡戊型肝炎病毒”、禽肝病毒和一些杯状病毒属成员中鉴定出的保守的48 nt“杠铃状”结构。一个预测的8592 nt的大开放阅读框(ORF)编码一个潜在的2864个氨基酸的多蛋白前体。此外,该病毒还包含一个预测的462个氨基酸的大L蛋白。成对序列比较以及系统发育分析显示与“雀形目病毒A”(以前称为火鸡戊型肝炎病毒1)的同一性百分比最高,在P1、P2和P3区域形成一个单系群,氨基酸同一性分别小于40%、40%和50%。与“鸡戊型肝炎病毒A”和杯状病毒属成员的同一性降低。定量PCR分析估计,在30份PCR阳性粪便中的22份(73%)中,病毒基因组拷贝数范围为4×10(5)至5×10(8)g(-1)。基于序列和系统发育分析,我们提出该病毒是小RNA病毒科一个潜在新属的首个成员。需要进一步研究以调查该病毒在禽类宿主中的致病潜力。