Suppr超能文献

感染克隆猿猴免疫缺陷病毒的猕猴出现反复的nef基因改变。

Macaques infected with cloned simian immunodeficiency virus show recurring nef gene alterations.

作者信息

Heidecker G, Muñoz H, Lloyd P, Hodge D, Ruscetti F W, Morton W R, Hu S, Benveniste R E

机构信息

SAIC Frederick, National Cancer Institute-Frederick Cancer Research and Development Center, Frederick, Maryland, 21702, USA.

出版信息

Virology. 1998 Sep 30;249(2):260-74. doi: 10.1006/viro.1998.9325.

Abstract

We compared nef gene sequences isolated by polymerase chain reaction from peripheral blood lymphocyte DNA of macaques that had been inoculated with either biologically (E11S) or molecularly (clone 8) cloned SIV/Mne. Two samples from each animal obtained either early (weeks 2-8) or late (weeks 21-137) after infection were analyzed. Three substitutions in the predicted Nef amino acid sequence were seen in all animals at the late time point, and two other substitutions were seen in all except one. Two of the common exchanges are located approximately 40 residues apart in the Nef core sequence but are juxtaposed on the tertiary structure as judged by computer modeling using the structure of the HIV Nef core protein as a guide. Most recurrent in vivo changes replaced a residue found in the cloned Nef sequence with one present in a consensus derived by aligning the Nef sequences of the SIV/Sm clade. Recombinant virus containing a macaque-adapted (MA nef) nef on the clone 8 backbone was 3-fold more infectious on SMAGI cells than the original virus. A lymphocyte line infected with SIV-clone 8-MAnef contained a large proportion of cells carrying provirus with defective nef genes. These findings suggest that the nef gene of the cloned SIV/Mne had undergone attenuating mutations during propagation in tissue culture that were "corrected" in vivo.

摘要

我们比较了通过聚合酶链反应从接种了生物克隆(E11S)或分子克隆(克隆8)的SIV/Mne的猕猴外周血淋巴细胞DNA中分离出的nef基因序列。分析了每只动物在感染后早期(第2 - 8周)或晚期(第21 - 137周)获得的两个样本。在晚期时间点,所有动物的预测Nef氨基酸序列中都出现了三个替换,除一只动物外,所有动物还出现了另外两个替换。两个常见的交换位于Nef核心序列中相距约40个残基处,但根据以HIV Nef核心蛋白结构为指导的计算机建模判断,它们在三级结构上是并列的。体内最常见的变化是将克隆的Nef序列中发现的一个残基替换为通过比对SIV/Sm分支的Nef序列得出的共有序列中的一个残基。在克隆8骨架上含有猕猴适应性(MA nef)nef的重组病毒在SMAGI细胞上的感染性比原始病毒高3倍。感染SIV - 克隆8 - MAnef的淋巴细胞系含有很大比例携带具有缺陷nef基因的前病毒的细胞。这些发现表明,克隆的SIV/Mne的nef基因在组织培养传播过程中发生了减毒突变,这些突变在体内被“校正”。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验