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Genomic diversity of the Avian leukosis virus subgroup J gp85 gene in different organs of an infected chicken

机译:禽白血病病毒J gp85亚群在感染鸡的不同器官中的基因组多样性

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The genomic diversity of Avian leukosis virus subgroup J (ALV-J) was investigated in an experimentally infected chicken. ALV-J variants in tissues from four different organs of the same bird were re-isolated in DF-1 cells, and their gp85 gene was amplified and cloned. Ten clones from each organ were sequenced and compared with the original inoculum strain, NX0101. The minimum homology of each organ ranged from 96.7 to 97.6%, and the lowest homology between organs was only 94.9%, which was much lower than the 99.1% homology of inoculum NX0101, indicating high diversity of ALV-J, even within the same bird. The gp85 mutations from the left kidney, which contained tumors, and the right kidney, which was tumor-free, had higher non-synonymous to synonymous mutation ratios than those in the tumor-bearing liver and lungs. Additionally, the mutational sites of gp85 gene in the kidney were similar, and they differed from those in the liver and lung, implying that organ-or tissue-specific selective pressure had a greater influence on the evolution of ALV-J diversity. These results suggest that more ALV-J clones from different organs and tissues should be sequenced and compared to better understand viral evolution and molecular epidemiology in the field.
机译:在实验感染的鸡中调查了禽白血病J亚组(ALV-J)的基因组多样性。将同一只鸟的四个不同器官的组织中的ALV-J变体重新分离到DF-1细胞中,并扩增和克隆了它们的gp85基因。对每个器官的十个克隆进行测序,并与原始接种菌株NX0101进行比较。每个器官的最小同源性在96.7%至97.6%之间,而器官之间的最低同源性仅为94.9%,远低于接种物NX0101的99.1%同源性,这表明即使在同一只禽类中,ALV-J的多样性也很高。与携带肿瘤的肝和肺相比,含有肿瘤的左肾和无肿瘤的右肾的gp85突变具有更高的非同义至同义突变比率。此外,肾脏中gp85基因的突变位点相似,与肝脏和肺中的突变位点不同,这意味着器官或组织特异性选择压力对ALV-J多样性的进化影响更大。这些结果表明,应该对来自不同器官和组织的更多ALV-J克隆进行测序并进行比较,以更好地了解该领域的病毒进化和分子流行病学。

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