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首页> 外文期刊>Virus Genes >Identification and characterization of a novel natural recombinant avian leucosis virus from Chinese indigenous chicken flock
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Identification and characterization of a novel natural recombinant avian leucosis virus from Chinese indigenous chicken flock

机译:来自中国土着鸡群新型天然重组禽白血病病毒的鉴定与表征

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摘要

Avian leukosis virus (ALV) caused tremendous economic losses to poultry industry all over the world, especially in China. One natural recombinant ALV strain, designated as HB2015032, was isolated from indigenous chickens with neoplastic diseases in Hubei, China. The complete proviral genome of HB2015032 is 7703 bp in length. Sequence analysis showed that the Env of HB2015032 exhibited 99.3% similarity with that of a ALV subgroup K (ALV-K) isolate JS11C1 at amino acid level. Phylogenetic analysis revealed that both gp85 and gp37 of HB2015032 were clustered in the same branch with JS11C1 and other ALV-K strains isolated from Chinese indigenous chickens in recent years. However, the pol gene, the 3 ' untranslated region (3 ' UTR), and the 3 ' long terminal repeat (3 ' LTR) of HB2015032 were more closely related to ALV-J prototype HPRS-103, and clustered in the same branch with ALV-J strains. Furthermore, the pol gene of HB2015032 contained a premature stop codon that resulted in a truncated Pol protein with 22 amino acid residues missing, which was a unique feature of the pol gene of ALV-J. 3 ' UTR of HB2015032 containing entire DR1, E element and U3. E element of HB2015032 contained one base deletion, which resulted in a c-Ets-1 binding site. In addition, U3 region of HB2015032 contains most of the transcription regulatory elements of ALV-J, including two CAAT boxes, Y boxes, CArG boxes, PRE boxes, NFAP-1 boxes, and one TATA box. These results suggest that isolate HB2015032 was a novel recombinant ALV-K containing the ALV-K env gene and the ALV-J backbone and exhibiting high pathogenicity.
机译:禽耳愈伤症病毒(ALV)引起了世界各地的家禽业的巨大经济损失,特别是在中国。一种自然重组Alv菌株,被指定为HB2015032,从湖北省肿瘤疾病中与土着鸡分离出来。 HB2015032的完整透过率基因组长度为7703bp。序列分析表明,HB2015032的enV表现出99.3%的相似性与ALV亚组K(ALV-K)分离在氨基酸水平下的相似性。系统发育分析显示,HB2015032的GP85和GP37近年来与JS11C1和其他Alv-k菌株中的相同分支聚集在同一分支中。但是,POL基因,3'未翻转区域(3'UTR)和3'长末端重复(3'LTR)的HB2015032更密切地与ALV-J原型HPRS-103相关,并在同一分支中聚集alv-j菌株。此外,HB2015032的POL基因含有过早的止动密码子,其导致截短的POL蛋白,其中缺少22个氨基酸残基,这是ALV-J的POL基因的独特特征。 3'UTR包含整个DR1,E元素和U3的HB2015032。 HB2015032的E元素含有一种基础缺失,导致C-ETE-1结合位点。此外,HB2015032的U3区域包含ALV-J的大部分转录调节元件,包括两个CAAT盒,Y盒,轿厢盒,预框,NFAP-1盒和一个TATA盒。这些结果表明,分离物HB2015032是含有Alv-k Env基因的新型重组Alv-k和Alv-J骨架并表现出高致病性。

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