首页> 美国卫生研究院文献>Journal of Virology >Size variation within the second hypervariable region of the surface envelope gene of the bovine lentivirus BIV in experimentally and naturally infected cattle.
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Size variation within the second hypervariable region of the surface envelope gene of the bovine lentivirus BIV in experimentally and naturally infected cattle.

机译:在实验性感染和自然感染的牛中牛慢病毒BIV的表面包膜基因第二个高变区内的大小变化。

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摘要

The bovine lentivirus also known as the bovine immunodeficiency-like virus (BIV) has conserved and hypervariable regions in the surface envelope (SU) gene. Size variation between isolates can be as large as 200 bp, mostly occurring in the second hypervariable (V2) gene region of the SU gene. The V2 region was cloned and sequenced from both experimentally and naturally infected cattle. Temporal evaluation of provirus from an experimentally inoculated cow showed two different-sized variants that appeared over time. The variation appeared to result from a recombinational event resulting in an apparent direct repeat. Cloned proviral nucleotide sequence diversity increased over time. Virus that was cultured and then cloned and sequenced showed progressive change from the inoculum virus, but culturing reduced the diversity of the clones as compared with direct amplification of provirus from leukocyte samples from the cow. The quasispecies phenomenon was evident in clones sequenced from a cow naturally infected with BIV. Of 10 clones examined from the V2 region, 6 different-size clones were present with nine different patterns of sequence rearrangement. Sequence length of different clones varied by as much as 43 amino acids (aa), with 21- and 15-aa direct repeats accounting for most of the size variation. Similar to other lentiviruses, BIV appears to mutate rapidly, which may be important in viral persistence and pathogenesis.
机译:牛慢病毒也称为牛免疫缺陷样病毒(BIV),在表面包膜(SU)基因中具有保守和高变区。分离株之间的大小差异可能高达200 bp,主要发生在SU基因的第二个高变(V2)基因区域。从实验和自然感染的牛中克隆并测序V2区。对来自实验接种牛的原病毒的时间评估显示了随时间推移出现的两个不同大小的变体。变异似乎是由重组事件导致的,该事件导致明显的直接重复。克隆的前病毒核苷酸序列多样性随时间增加。经过培养然后克隆和测序的病毒显示出与接种病毒相比逐渐发生变化,但是与从牛白细胞样本中直接扩增原病毒相比,培养降低了克隆的多样性。在从自然感染了BIV的母牛中测序得到的克隆中,明显存在准种现象。在来自V2区域的10个克隆中,存在6个不同大小的克隆,具有9种不同的序列重排模式。不同克隆的序列长度相差多达43个氨基酸(aa),其中21-和15-aa直接重复占了大部分大小差异。与其他慢病毒相似,BIV似乎快速突变,这可能对病毒的持久性和发病机制很重要。

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