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来自猿猴免疫缺陷病毒的Nef蛋白是束缚素拮抗剂。

Nef proteins from simian immunodeficiency viruses are tetherin antagonists.

作者信息

Zhang Fengwen, Wilson Sam J, Landford Wilmina C, Virgen Beatriz, Gregory Devon, Johnson Marc C, Munch Jan, Kirchhoff Frank, Bieniasz Paul D, Hatziioannou Theodora

机构信息

Aaron Diamond AIDS Research Center, Laboratory of Retrovirology, the Rockefeller University, New York, NY 10016, USA.

出版信息

Cell Host Microbe. 2009 Jul 23;6(1):54-67. doi: 10.1016/j.chom.2009.05.008. Epub 2009 Jun 4.

Abstract

The tetherin/BST2/CD317 protein blocks the release of HIV-1 and other enveloped viruses by inducing tethering of nascent particles to infected cell surfaces. The HIV-1 Vpu protein antagonizes the antiviral activity of human but not monkey tetherins and many simian immunodeficiency viruses (SIVs) do not encode Vpu. Here, we show that the apparently "missing" antitetherin activity in SIVs has been acquired by several SIV Nef proteins. Specifically, SIV(MAC)/SIV(SMM), SIV(AGM), and SIV(BLU) Nef proteins can suppress tetherin activity. Notably, tetherin antagonism by SIV Nef proteins is species specific, is genetically separable from other Nef activities, and is most evident with simian rather than human tetherin proteins. Accordingly, a critical determinant of sensitivity to SIV(MAC) Nef in the tetherin cytoplasmic tail is variable in nonhuman primate tetherins and deleted in human tetherin, likely due to selective pressures imposed by viral antagonists, perhaps including Nef proteins.

摘要

束缚素/BST2/CD317蛋白通过诱导新生病毒颗粒与受感染细胞表面的连接,来阻止HIV-1和其他包膜病毒的释放。HIV-1的Vpu蛋白可拮抗人类而非猴类束缚素的抗病毒活性,并且许多猴免疫缺陷病毒(SIV)不编码Vpu。在此,我们表明几种SIV Nef蛋白获得了SIV中明显“缺失”的抗束缚素活性。具体而言,SIV(MAC)/SIV(SMM)、SIV(AGM)和SIV(BLU)的Nef蛋白可抑制束缚素活性。值得注意的是,SIV Nef蛋白对束缚素的拮抗作用具有物种特异性,在遗传上可与其他Nef活性分离,并且在猴类而非人类束缚素蛋白中最为明显。因此,束缚素细胞质尾巴中对SIV(MAC)Nef敏感的关键决定因素在非人类灵长类动物束缚素中是可变的,而在人类束缚素中缺失,这可能是由于病毒拮抗剂(可能包括Nef蛋白)施加的选择压力所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a3c/2852097/12595e534175/nihms186230f1.jpg

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