首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Isolation and genomic characterization of a classical Muscovy duck reovirus isolated in Zhejiang, China
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Isolation and genomic characterization of a classical Muscovy duck reovirus isolated in Zhejiang, China

机译:中国浙江分离的经典番鸭呼肠孤病毒的分离和基因组学鉴定

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A classical Muscovy reovirus was isolated from a sick Muscovy duck with white necrotic foci in its liver in Zhejiang, China, in 2000. This classical reovirus was propagated in a chicken fibroblast cell line (DF-1) with obvious cytopathic effects. Its genome was 22,967 bp in length, with approximately 51.41% G + C content and 10 dsRNA segments encoding 11 proteins, which formed a 3/3/4 electrophoretic PAGE profile pattern. The length of the genomic segments was similar to those of avian orthoreoviruses (ARV and N-MDRV), ranging from 3959 nt (L1) to 1191 nt (S4). All of the segments have the conserved terminal sequences 5'-GCUUUU-UUCAUC-3', and with the exception of the S4 segment, all the genome segments apparently encode one single primary translation product. The genome analysis revealed that the S4 segment of classical MDRV is a bicistronic gene, encoding the overlapping ORFs for p10 and sigma C but distinct from ARV and N-MDRV/N-GRV, which codes for p10, p18 and sigma C via the tricistronic S1 segment. A comparative sequence analysis provided evidence indicating extensive sequence divergence between classical MDRV and other avian orthoreoviruses. A phylogenetic analysis based on the RNA-dependent RNA polymerase (RdRp) and the major outer capsid proteins sigma C was performed. Members of the DRVs in the Avian orthoreovirus species were clustered into two genetic groups (classical MDRV and N-MDRV genotype), and the classical MDRV isolates formed distinct lineages (China and Europe lineages), suggesting that the classical MDRVs isolated in restricted geographical region are evolving by different and independent pathways
机译:2000年,从中国浙江省肝脏中有白色坏死灶的番鸭中分离出经典的莫斯科呼肠孤病毒。该经典的呼肠孤病毒在鸡成纤维细胞系(DF-1)中繁殖,具有明显的细胞病变作用。它的基因组长度为22967 bp,具有大约51.41%的G + C含量和10个编码11种蛋白质的dsRNA片段,形成了3/3/4电泳PAGE谱图。基因组片段的长度与禽正咽病毒(ARV和N-MDRV)相似,范围为3959 nt(L1)至1191 nt(S4)。所有区段均具有保守的末端序列5'-GCUUUU-UUCAUC-3',并且除了S4区段外,所有基因组区段显然编码一个单一的初级翻译产物。基因组分析显示,经典MDRV的S4片段是双顺反子基因,编码p10和sigma C的ORF重叠,但不同于ARV和N-MDRV / N-GRV,后者通过三顺反子编码p10,p18和sigma C S1段。比较序列分析提供了证据,表明经典MDRV与其他禽正咽病毒之间存在广泛的序列差异。基于RNA依赖性RNA聚合酶(RdRp)和主要外衣壳蛋白sigma C进行了系统发育分析。禽正咽病毒物种中DRV的成员被分为两个基因组(经典MDRV和N-MDRV基因型),经典MDRV分离株形成了不同的谱系(中国和欧洲谱系),这表明经典MDRV在有限的地理区域内分离正在通过不同且独立的途径发展

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