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首页> 外文期刊>Virology >Simian adenovirus type 35 has a recombinant genome comprising human and simian adenovirus sequences, which predicts its potential emergence as a human respiratory pathogen
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Simian adenovirus type 35 has a recombinant genome comprising human and simian adenovirus sequences, which predicts its potential emergence as a human respiratory pathogen

机译:35型猿猴腺病毒具有包含人和猿猴腺病毒序列的重组基因组,可预测其可能作为人类呼吸道病原体出现

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Emergent human and simian adenoviruses (HAdVs) may arise from genome recombination. Computational analysis of SAdV type 35 reveals a genome comprising a chassis with elements mostly from two simian adenoviruses, SAdV-B21 and -B27, and regions of high sequence similarity shared with HAdV-B21 and HAdV-B16. Although recombination direction cannot be determined, the presence of these regions suggests prior infections of humans by an ancestor of SAdV-B35, and/or vice versa. Absence of this virus in humans may reflect non-optimal conditions for zoonosis or incomplete typing, e.g., limited epitope-based. The presence of both a critical viral replication element found in HAdV genomes and genes that are highly similar to ones in HAdVs suggest the potential to establish in a human host. This allows a prediction that this virus may be a nascent human respiratory pathogen. The recombination potential of human and simian adenovirus genomes should be considered in the use of SAdVs as vectors for gene delivery in humans.
机译:新兴的人类和猿猴腺病毒(HAdV)可能来自基因组重组。对35型SAdV的计算分析揭示了一个基因组,该基因组包含一个底盘,该底盘具有主要来自两种猿猴腺病毒SAdV-B21和-B27的元件,以及与HAdV-B21和HAdV-B16共享的高序列相似性区域。尽管不能确定重组方向,但是这些区域的存在表明人先前曾被SAdV-B35的祖先感染,反之亦然。在人类中不存在这种病毒可能反映出人畜共患病或分型不全(例如基于有限的表位)的非最佳条件。在HAdV基因组中发现的关键病毒复制元件以及与HAdV中的基因高度相似的基因均表明存在在人宿主中建立潜能的潜力。这样可以预测该病毒可能是新生的人类呼吸道病原体。在使用SAdV作为人类基因传递载体时,应考虑人类和猿猴腺病毒基因组的重组潜力。

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