The Ebola virus glycoprotein and HIV-1 Vpu employ different strategies to counteract the antiviral factor tetherin.

The Ebola virus glycoprotein and HIV-1 Vpu employ different strategies to counteract the antiviral factor tetherin.
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埃博拉病毒糖蛋白和HIV-1 VPU采用不同的策略来抵消抗病毒因子Tetherin。

DOI:
10.1093/infdis/jir378
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发表时间:
2011-11
期刊:
The Journal of infectious diseases
影响因子:
--
通讯作者:
Pöhlmann S
Pöhlmann S
中科院分区:
其他
文献类型:
--
作者:
Kühl A;Banning C;Marzi A;Votteler J;Steffen I;Bertram S;Glowacka I;Konrad A;Stürzl M;Guo JT;Schubert U;Feldmann H;Behrens G;Schindler M;Pöhlmann S

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The antiviral protein tetherin/BST2/CD317/HM1.24 restricts cellular egress of human immunodeficiency virus (HIV) and of particles mimicking the Ebola virus (EBOV), a hemorrhagic fever virus. The HIV-1 viral protein U (Vpu) and the EBOV-glycoprotein (EBOV-GP) both inhibit tetherin. Here, we compared tetherin counteraction by EBOV-GP and Vpu. We found that EBOV-GP but not Vpu counteracted tetherin from different primate species, indicating that EBOV-GP and Vpu target tetherin differentially. Tetherin interacted with the GP2 subunit of EBOV-GP, which might encode the determinants for tetherin counteraction. Vpu reduced cell surface expression of tetherin while EBOV-GP did not, suggesting that both proteins employ different mechanisms to counteract tetherin. Finally, Marburg virus (MARV)–GP also inhibited tetherin and downregulated tetherin in a cell type–dependent fashion, indicating that tetherin antagonism depends on the cellular source of tetherin. Collectively, our results indicate that EBOV-GP counteracts tetherin by a novel mechanism and that tetherin inhibition is conserved between EBOV-GP and MARV-GP.
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