SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4+ T-cells

被引:284
作者
Descours, Benjamin [1 ]
Cribier, Alexandra [1 ]
Chable-Bessia, Christine [1 ]
Ayinde, Diana [3 ]
Rice, Gillian [2 ]
Crow, Yanick [2 ]
Yatim, Ahmad [1 ]
Schwartz, Olivier [3 ]
Laguette, Nadine [1 ]
Benkirane, Monsef [1 ]
机构
[1] CNRS, Inst Genet Humaine, Mol Virol Lab, UPR1142, Montpellier, France
[2] Univ Manchester, Acad Unit Med Genet, Manchester, Lancs, England
[3] Inst Pasteur, Virus & Immun Unit, CNRS, URA 3015, Paris, France
基金
欧洲研究理事会;
关键词
SAMHD1; Quiescent CD4(+) T-cell; HIV-1; Reverse transcription; Restriction; IMMUNODEFICIENCY-VIRUS TYPE-1; INFECTION; REPLICATION; LYMPHOCYTES; ESTABLISHMENT; ACTIVATION; PROTEIN; LATENCY; LEVEL; DNA;
D O I
10.1186/1742-4690-9-87
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Background: Quiescent CD4(+) T lymphocytes are highly refractory to HIV-1 infection due to a block at reverse transcription. Results: Examination of SAMHD1 expression in peripheral blood lymphocytes shows that SAMHD1 is expressed in both CD4+ and CD8+ T cells at levels comparable to those found in myeloid cells. Treatment of CD4+ T cells with Virus-Like Particles (VLP) containing Vpx results in the loss of SAMHD1 expression that correlates with an increased permissiveness to HIV-1 infection and accumulation of reverse transcribed viral DNA without promoting transcription from the viral LTR. Importantly, CD4(+) T-cells from patients with Aicardi-Goutieres Syndrome harboring mutation in the SAMHD1 gene display an increased susceptibility to HIV-1 infection that is not further enhanced by VLP-Vpx-treatment. Conclusion: Here, we identified SAMHD1 as the restriction factor preventing efficient viral DNA synthesis in non-cycling resting CD4(+) T-cells. These results highlight the crucial role of SAMHD1 in mediating restriction of HIV-1 infection in quiescent CD4(+) T-cells and could impact our understanding of HIV-1 mediated CD4(+) T-cell depletion and establishment of the viral reservoir, two of the HIV/AIDS hallmarks.
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