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Poxviral E3L ortholog (Viral Interferon resistance gene) of orf viruses of sheep and goats indicates species-specific clustering with heterogeneity among parapoxviruses

机译:绵羊和山羊的ORF病毒的POxViral E3L Ortholog(病毒干扰素抗性基因)表明帕拉斯普血管病毒之间的物种特异性聚类具有异质性

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摘要

Orf is a contagious disease posing a serious threat to animal and human health. E3L is one of the evolutionarily acquired immunomodulatory proteins present in orf virus (ORFV) and is responsible for conferring resistance to interferons among poxviruses. Genetic analysis of ORFV isolates of different geographical regions including Indian subcontinent targeting viral interferon resistance (VIR) gene (a homolog of vaccinia virus E3L gene) revealed a high percentage of identity among themselves and other ORFV isolates at both nt and as levels as compared to low identity among parapoxviruses (PPVs). Phylogenetic analysis showed species-specific clustering among PPVs along with sub-clusters based on host species of origin among OREVs infecting sheep and goats. Conserved amino acids in N-terminal Z-DNA binding domain and C-terminal ds RNA binding domain of VIR proteins of PPVs corresponding to ORFV VIR positions namely N37, Y41, P57, and W59 (necessary for Z-DNA binding) and E116, F127, F141, and K160 (necessary for dsRNA binding) were found. Further, the predicted protein characteristics and homology model of VIR protein of ORFV showed high structural conservation among poxviruses. This study on E3L genetic analysis of ORFV isolates may provide a better understanding of the molecular epidemiology of circulating strains in India and neighboring countries. Also, E3L deleted or mutated ORFV may be an as vaccine candidate and/or compounds blocking E3L may prove as an effective method for treating broad spectrum poxviral infections, suggesting a wider application in control of poxvirus infections.
机译:ORF是一种传染病,对动物和人类健康构成严重威胁。 E3L是在ORF病毒(ORFV)中存在的进化获得的免疫调节蛋白之一,并且负责赋予痘病毒之间的干扰素抵抗力。不同地理区域的ORFV分离物的遗传分析,包括印度次大陆靶向病毒干扰素抗性(VIR)基因(疫苗病毒E3L基因的同源物)揭示了它们在NT和作为水平的含量和水平的高百分比parapoxviruses(ppvs)之间的身份低。系统发育分析显示了PPV的物种特异性聚类以及基于感染绵羊和山羊的宿主宿主物种的子簇。 N-末端Z-DNA结合结构域的保守氨基酸和PPVS的VIR蛋白的C-末端DS RNA结合结构域对应于ORFV VIR位置即N37,Y41,P57和W59(Z-DNA结合所必需)和E116,发现F127,F141和K160(DSRNA结合所必需的)。此外,ORFV的VIR蛋白的预测蛋白质特征和同源性模型显示出痘病毒的高结构保护。本研究orfV分离物的E3L遗传分析可以更好地了解印度和邻国循环菌株的分子流行病学。而且,E3L缺失或突变的orfv可以是疫苗候选和/或封闭E3L的化合物可以证明是治疗广谱痘病毒感染的有效方法,这表明对痘病毒感染的控制更广泛。

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