4.7 Article

Nef Proteins from Simian Immunodeficiency Viruses Are Tetherin Antagonists

Journal

CELL HOST & MICROBE
Volume 6, Issue 1, Pages 54-67

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2009.05.008

Keywords

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Funding

  1. NIH [R01AI078788, R01AI050111, R01AI067057]
  2. Deutsche Forschungsgemeinschaft
  3. Howard Hughes Medical Institute.

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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, SIVMAC/SIVSMM, SIVAGM, and SIVBLU 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 SIVMAC 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.

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