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来自终末期疾病的原发性HIV-1 R5分离株显示出病毒适应性增强,同时gp120净电荷增加。

Primary HIV-1 R5 isolates from end-stage disease display enhanced viral fitness in parallel with increased gp120 net charge.

作者信息

Repits Johanna, Sterjovski Jasminka, Badia-Martinez Daniel, Mild Mattias, Gray Lachlan, Churchill Melissa J, Purcell Damian F J, Karlsson Anders, Albert Jan, Fenyö Eva Maria, Achour Adnane, Gorry Paul R, Jansson Marianne

机构信息

Department of Laboratory Medicine, Lund University, Sweden.

出版信息

Virology. 2008 Sep 15;379(1):125-34. doi: 10.1016/j.virol.2008.06.014. Epub 2008 Jul 30.

Abstract

To better understand the evolution of the viral envelope glycoproteins (Env) in HIV-1 infected individuals who progress to AIDS maintaining an exclusive CCR5-using (R5) virus population, we cloned and sequenced the env gene of longitudinally obtained primary isolates. A shift in the electrostatic potential towards an increased net positive charge was revealed in gp120 of end-stage viruses. Residues with increased positive charge were primarily localized in the gp120 variable regions, with the exception of the V3 loop. Molecular modeling indicated that the modifications clustered on the gp120 surface. Furthermore, correlations between increased Env net charge and lowered CD4(+) T cell counts, enhanced viral fitness, reduced sensitivity to entry inhibitors and augmented cell attachment were disclosed. In summary, this study suggests that R5 HIV-1 variants with increased gp120 net charge emerge in an opportunistic manner during severe immunodeficiency. Thus, we here propose a new mechanism by which HIV-1 may gain fitness.

摘要

为了更好地理解在进展为艾滋病的HIV-1感染个体中,维持单一使用CCR5(R5)病毒群体时病毒包膜糖蛋白(Env)的进化情况,我们克隆并测序了纵向获取的原代分离株的env基因。在晚期病毒的gp120中发现静电势向净正电荷增加的方向转变。正电荷增加的残基主要位于gp120可变区,但V3环除外。分子建模表明,这些修饰聚集在gp120表面。此外,还揭示了Env净电荷增加与CD4(+) T细胞计数降低、病毒适应性增强、对进入抑制剂敏感性降低以及细胞附着增加之间的相关性。总之,本研究表明,在严重免疫缺陷期间,gp120净电荷增加的R5 HIV-1变体以机会性方式出现。因此,我们在此提出一种HIV-1可能获得适应性的新机制。

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