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山羊维斯纳病毒:一种与绵羊维斯纳病毒相关的逆转录病毒的分离

Goat visna virus: isolation of a retrovirus related to visna virus of sheep.

作者信息

Sundquist B

出版信息

Arch Virol. 1981;68(2):115-27. doi: 10.1007/BF01314441.

Abstract

Choroid plexus (GCP-3) cell cultures were prepared from an adult goat with symptoms of visna. The GCP-3 cell layer had partly fused into large multinucleated giant cells and electronmicrographs showed virus particles morphologically indistinguishable from sheep visna virus (SVV). A virus, designated goat visna virus (GVV), was subsequently purified from the GCP-3 cultures. The virus particles have a density of 1.15 g/ml and a high molecular weight RNA similar in size to that of SVV. A virion-associated DNA polymerase was identified which is stimulated to the same extent as the SVV polymerase by different synthetic RNA and DNA template-primer combinations and which shows the same Mg2+ and Mn2+ stimulation optima. Polypeptide analysis by SDS-PAGE revealed that the virion proteins of GVV and SVV had similar molecular weights. By immunodiffusion tests it was demonstrated that the major internal proteins of GVV and SVV are related. Consequently, we conclude that GVV should be classified as a retrovirus and that it is closely related to visna virus of sheep.

摘要

脉络丛(GCP - 3)细胞培养物取自一只出现维斯纳症状的成年山羊。GCP - 3细胞层部分融合形成了大型多核巨细胞,电子显微镜照片显示病毒颗粒在形态上与绵羊维斯纳病毒(SVV)无法区分。随后从GCP - 3培养物中纯化出一种病毒,命名为山羊维斯纳病毒(GVV)。病毒颗粒的密度为1.15 g/ml,具有与SVV大小相似的高分子量RNA。鉴定出一种病毒粒子相关的DNA聚合酶,它被不同的合成RNA和DNA模板 - 引物组合刺激的程度与SVV聚合酶相同,并且显示出相同的Mg2 +和Mn2 +刺激最佳值。通过SDS - PAGE进行的多肽分析表明,GVV和SVV的病毒粒子蛋白具有相似的分子量。通过免疫扩散试验证明,GVV和SVV的主要内部蛋白是相关的。因此,我们得出结论,GVV应归类为逆转录病毒,并且它与绵羊的维斯纳病毒密切相关。

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