A virus-packageable CRISPR screen identifies host factors mediating interferon inhibition of HIV

被引:103
作者
OhAinle, Molly [1 ,2 ]
Helms, Louisa [1 ,2 ]
Vermeire, Jolien [1 ,2 ]
Roesch, Ferdinand [1 ,2 ]
Humes, Daryl [1 ,2 ]
Basom, Ryan [3 ]
Delrow, Jeffrey J. [3 ]
Overbaugh, Julie [1 ,2 ]
Emerman, Michael [1 ,2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Human Biol, Washington, DC USA
[2] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Washington, DC USA
[3] Fred Hutchinson Canc Res Ctr, Genom & Bioinformat Shared Resource, 1124 Columbia St, Seattle, WA 98104 USA
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; HUMAN TRIM5-ALPHA; RESTRICTION FACTORS; TYPE-1; REPLICATION; ADAPTIVE EVOLUTION; CELL SPREAD; T-CELLS; PROTEIN; INFECTION; GENE;
D O I
10.7554/eLife.39823
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interferon (IFN) inhibits HIV replication by inducing antiviral effectors. To comprehensively identify IFN-induced HIV restriction factors, we assembled a CRISPR sgRNA library of Interferon Stimulated Genes (ISGs) into a modified lentiviral vector that allows for packaging of sgRNA-encoding genomes in trans into budding HIV-1 particles. We observed that knockout of Zinc Antiviral Protein (ZAP) improved the performance of the screen due to ZAP-mediated inhibition of the vector. A small panel of IFN-induced HIV restriction factors, including MxB, IFITM1, Tetherin/BST2 and TRIM5alpha together explain the inhibitory effects of IFN on the CXCR4-tropic HIV-1 strain, HIV-1(LAI), in THP-1 cells. A second screen with a CCR5-tropic primary strain, HIV-1(Q23.BG505), described an overlapping, but non-identical, panel of restriction factors. Further, this screen also identifies HIV dependency factors. The ability of IFN-induced restriction factors to inhibit HIV strains to replicate in human cells suggests that these human restriction factors are incompletely antagonized.
引用
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页数:32
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