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人内源性逆转录病毒-K108包膜蛋白的表达会干扰HIV-1的产生。

Expression of HERV-K108 envelope interferes with HIV-1 production.

作者信息

Terry Sandra N, Manganaro Lara, Cuesta-Dominguez Alvaro, Brinzevich Daria, Simon Viviana, Mulder Lubbertus C F

机构信息

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Division of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Virology. 2017 Sep;509:52-59. doi: 10.1016/j.virol.2017.06.004. Epub 2017 Jun 9.

Abstract

The human endogenous retroviruses (HERV)-K of the HML-2 group include full-length or near full-length elements encoding functional proteins, and are classified as type-1 or type-2 (type-1 has a deletion in the 5' end of the env gene). Because proteins of different retroviruses can interact, we hypothesized that HERV-K envelope (Env) could influence HIV-1 replication. Here we describe the negative effect of envelope expression of certain type-2 HERV-Ks on HIV-1 production. All HIV-1 and SIV strains tested were susceptible to various degrees to inhibition by the HERV-K108 envelope. We identified four residues within HERV-K108 Env as being critical to inhibit HIV-1 production. No inhibition was observed on EGFP expression, indicating that HERV-K Env does not affect general protein production. These findings demonstrate that envelope proteins from some endogenous retroviruses can limit production of exogenous lentiviruses such as HIV-1. Future studies will elucidate the mechanism mediating HIV-1 inhibition by HERV Envs.

摘要

HML-2组的人类内源性逆转录病毒(HERV)-K包含编码功能蛋白的全长或接近全长元件,分为1型或2型(1型在env基因的5'端有缺失)。由于不同逆转录病毒的蛋白可以相互作用,我们推测HERV-K包膜(Env)可能影响HIV-1复制。在此,我们描述了某些2型HERV-K的包膜表达对HIV-1产生的负面影响。所有测试的HIV-1和SIV毒株都不同程度地易受HERV-K108包膜的抑制。我们确定HERV-K108 Env中的四个残基对抑制HIV-1产生至关重要。未观察到对EGFP表达的抑制,表明HERV-K Env不影响一般蛋白质的产生。这些发现表明,一些内源性逆转录病毒的包膜蛋白可以限制外源性慢病毒如HIV-1的产生。未来的研究将阐明HERV Env介导HIV-1抑制的机制。

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