HIV-1 Antagonism of CD317 Is Species Specific and Involves Vpu-Mediated Proteasomal Degradation of the Restriction Factor
HIV-1 Antagonism of CD317 Is Species Specific and Involves Vpu-Mediated Proteasomal Degradation of the Restriction Factor
Mammals encode proteins that inhibit viral replication at the cellular level. In turn, certain viruses have evolved genes that can functionally counteract these intrinsic restrictions. Human CD317 (BST-2/HM1.24/tetherin) is a restriction factor that blocks release of human immunodeficiency virus type 1 (HIV-1) from the cell surface and can be overcome by HIV-1 Vpu. Here, we show that mouse and rat CD317 potently inhibit HIV-1 release but are resistant to Vpu. Interspecies chimeras reveal that the rodent-specific resistance and human-specific sensitivity to Vpu antagonism involve all three major structural domains of CD317. To promote virus release, Vpu depletes cellular pools of human CD317, but not of the rodent orthologs, by accelerating its degradation via the 20S proteasome. Thus, HIV-1 Vpu suppresses the expression of the CD317 antiviral factor in human cells, and the species-specific resistance to this suppression may guide the development of small animal models of HIV infection.
- University of Bristol
- University of Bristol
- European Bioinformatics Institute United Kingdom
- Department of Biochemistry Switzerland
- University of Bristol
Cancer Research, MICROBIO, Membrane Glycoproteins, Virulence Factors, Human Immunodeficiency Virus Proteins, 610, GPI-Linked Proteins, Cell Line, Rats, Mice, Antigens, CD, Immunology and Microbiology(all), HIV-1, Animals, Humans, Viral Regulatory and Accessory Proteins, MOLIMMUNO, Molecular Biology
Cancer Research, MICROBIO, Membrane Glycoproteins, Virulence Factors, Human Immunodeficiency Virus Proteins, 610, GPI-Linked Proteins, Cell Line, Rats, Mice, Antigens, CD, Immunology and Microbiology(all), HIV-1, Animals, Humans, Viral Regulatory and Accessory Proteins, MOLIMMUNO, Molecular Biology
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