Department of Virology and Antiviral Therapy, Jena University Hospital, Friedrich Schiller University, Hans Knoell Str. 2, 07745 Jena, Germany.
Genome Analysis, Leibniz Institute for Age Research, Fritz Lipmann Institute, Beutenbergstrasse 11, 07745 Jena, Germany.
J Gen Virol. 2014 Jan;95(Pt 1):80-90. doi: 10.1099/vir.0.058172-0.
Picornaviruses have been isolated from a variety of hosts, mainly mammals and birds. Here, we describe the sequence analysis of carp picornavirus 1 (CPV-1) F37/06 that was isolated from an organ pool (heart, brain, liver) of a common carp (Cyprinus carpio). This carp perished after an accidental discharge of liquid manure into a fish pond and presented without obvious clinical symptoms. Experimental intraperitoneal infection of young carp with CPV-1 revealed no clinical signs, but the virus was re-isolated from various organs. Sequence analysis of almost the complete genome (7632 nt excluding the poly-A tract) revealed a novel picornavirus clade. In phylogenetic trees, the polymerase sequence clusters with parechoviruses, duck hepatitis A virus, eel picornavirus and aquamavirus A. The ORF includes 6807 nt and encodes a polyprotein of 2269 amino acids. CPV-1 has a genome layout like that of picornaviruses except for the presence of two aphthovirus 2A-like NPGP sequence motifs: VPg+5'UTR[1AB-1C-1D-2A1(npgp)/2A2(npgp)-2B-2C(ATPase)/3A-3B(VPg)-3C(pro)-3D(pol)]3'UTR-poly-A. 2A1(npgp) and 2A2(npgp) are separated by 133 amino acids. The proteins 2A2(npgp), 2B, 3A and 3B(VPg) have no significant similarity to the corresponding proteins of other picornaviruses. Amino acid identities of the orthologous proteins P1, 2C, 3C(pro) and 3D(pol) range from 16.4 to 40.8 % in the eel picornavirus/CPV-1 comparison. 3D(pol) shows the closest similarity to eel picornavirus, with an amino acid identity of 40.8 %, followed by human parechovirus (36.5 %), duck hepatitis A virus (32.7 %) and swine pasivirus (29.3 %). Both the unique genome organization and low sequence similarity support the assignment of CPV-1 to a novel picornavirus species within a novel genus.
小 RNA 病毒已从多种宿主中分离出来,主要是哺乳动物和鸟类。在这里,我们描述了从一尾鲤鱼(Cyprinus carpio)的器官池中分离出的鲤鱼小 RNA 病毒 1(CPV-1)F37/06 的序列分析。这尾鲤鱼在粪便意外排放到鱼塘后死亡,没有明显的临床症状。对 CPV-1 进行的年轻鲤鱼的实验性腹腔内感染未显示出临床症状,但该病毒从各种器官中重新分离出来。几乎完整基因组(不含多聚 A 区的 7632nt)的序列分析揭示了一个新的小 RNA 病毒进化枝。在系统发育树中,聚合酶序列与肠道病毒、鸭肝炎病毒、鳗鱼小 RNA 病毒和 Aquamavirus A 聚类。ORF 包含 6807nt,编码 2269 个氨基酸的多蛋白。CPV-1 的基因组布局与小 RNA 病毒相似,但存在两个口疮病毒 2A 样 NPGP 序列基序:VPg+5'UTR[1AB-1C-1D-2A1(npgp)/2A2(npgp)-2B-2C(ATPase)/3A-3B(VPg)-3C(pro)-3D(pol)]3'UTR-多聚 A。2A1(npgp)和 2A2(npgp)之间相隔 133 个氨基酸。2A2(npgp)、2B、3A 和 3B(VPg)的蛋白质与其他小 RNA 病毒的相应蛋白质没有显著相似性。鳗鱼小 RNA 病毒/CPV-1 比较中,直系同源蛋白 P1、2C、3C(pro)和 3D(pol)的氨基酸同一性范围为 16.4%至 40.8%。3D(pol)与鳗鱼小 RNA 病毒的相似度最高,氨基酸同一性为 40.8%,其次为人肠道病毒(36.5%)、鸭肝炎病毒(32.7%)和猪帕西病毒(29.3%)。独特的基因组结构和低序列相似性均支持将 CPV-1 分配到一个新的小 RNA 病毒属中的新型小 RNA 病毒种。