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BST-2/tetherin: a new component of the innate immune response to enveloped viruses
Ist Teil von
Trends in microbiology (Regular ed.), 2010-09, Vol.18 (9), p.388-396
Ort / Verlag
England: Elsevier Ltd
Erscheinungsjahr
2010
Link zum Volltext
Quelle
Elsevier ScienceDirect Journals
Beschreibungen/Notizen
The interferon-inducible, transmembrane protein BST-2 (CD317, tetherin) directly holds fully formed enveloped virus particles to the cells that produce them, inhibiting their spread. BST-2 inhibits members of the retrovirus, filovirus, arenavirus and herpesvirus families. These viruses encode a variety of proteins to degrade BST-2 and/or direct it away from its site of action at the cell surface. Viral antagonism has subjected BST-2 to positive selection, leading to species-specific differences that presented a barrier to the transmission of simian immunodeficiency viruses (SIVs) to humans. This barrier was crossed by HIV-1 when its Vpu protein acquired activity as a BST-2 antagonist. Here, we review this new host–pathogen relationship and discuss its impact on the evolution of primate lentiviruses and the origins of the HIV pandemic.