Restriction of diverse retroviruses by SAMHD1

被引:132
作者
Gramberg, Thomas [1 ,2 ]
Kahle, Tanja [2 ]
Bloch, Nicolin [1 ]
Wittmann, Sabine [2 ]
Muellers, Erik [3 ]
Daddacha, Waaqo [4 ]
Hofmann, Henning [1 ]
Kim, Baek [4 ]
Lindemann, Dirk [3 ]
Landau, Nathaniel R. [1 ]
机构
[1] NYU, Sch Med, Dept Microbiol, New York, NY 10016 USA
[2] Univ Erlangen Nurnberg, Inst Virol, D-91054 Erlangen, Germany
[3] Tech Univ Dresden, Inst Virol, Med Fak Carl Gustav Carus, D-01062 Dresden, Germany
[4] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USA
基金
美国国家卫生研究院;
关键词
HIV; SAMHD1; Macrophages; Vpx; Dendritic cells; Accessory proteins; IMMUNODEFICIENCY-VIRUS TYPE-1; INFECTIOUS-ANEMIA VIRUS; DENDRITIC CELLS; ENVELOPE PROTEIN; VPX; HIV-1; REPLICATION; GENE; MACROPHAGES; VECTORS;
D O I
10.1186/1742-4690-10-26
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Background: SAMHD1 is a triphosphohydrolase that restricts the replication of HIV-1 and SIV in myeloid cells. In macrophages and dendritic cells, SAMHD1 restricts virus replication by diminishing the deoxynucleotide triphosphate pool to a level below that which supports lentiviral reverse transcription. HIV-2 and related SIVs encode the accessory protein Vpx to induce the proteasomal degradation of SAMHD1 following virus entry. While SAMHD1 has been shown to restrict HIV-1 and SIV, the breadth of its restriction is not known and whether other viruses have a means to counteract the restriction has not been determined. Results: We show that SAMHD1 restricts a wide array of divergent retroviruses, including the alpha, beta and gamma classes. Murine leukemia virus was restricted by SAMHD1 in macrophages yet removal of SAMHD1 did not alleviate the block to infection because of an additional block to viral nuclear import. Prototype foamy virus (PFV) and Human T cell leukemia virus type I (HTLV-1) were the only retroviruses tested that were not restricted by SAMHD1. PFV reverse transcribes predominantly prior to entry and thus is unaffected by the dNTP level in the target cell. It is possible that HTLV-1 has a mechanism to render the virus resistant to SAMHD1-mediated restriction. Conclusion: The results suggest that SAMHD1 has broad anti-retroviral activity against which most viruses have not found an escape.
引用
收藏
页数:12
相关论文
共 46 条
[1]
A conserved dileucine-containing motif in p6gag governs the particle association of Vpx and Vpr of simian immunodeficiency viruses SIVmac and SIVagm [J].
Accola, MA ;
Bukovsky, AA ;
Jones, MS ;
Gottlinger, HG .
JOURNAL OF VIROLOGY, 1999, 73 (12) :9992-9999
[2]
Functional analysis of human spuma retrovirus genome [J].
Adachi, A ;
Sakai, H ;
Tokunaga, K ;
Kawamura, M .
VIRUS GENES, 1995, 11 (01) :15-20
[3]
The HD domain defines a new superfamily of metal-dependent phosphohydrolases [J].
Aravind, L ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (12) :469-472
[4]
Human gene therapy vectors derived from feline lentiviruses [J].
Barraza, Roman A. ;
Poeschla, Eric M. .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2008, 123 (1-2) :23-31
[5]
SAMHD1-Deficient CD14+ Cells from Individuals with Aicardi-Goutieres Syndrome Are Highly Susceptible to HIV-1 Infection [J].
Berger, Andre ;
Sommer, Andreas F. R. ;
Zwarg, Jenny ;
Hamdorf, Matthias ;
Welzel, Karin ;
Esly, Nicole ;
Panitz, Sylvia ;
Reuter, Andreas ;
Ramos, Irene ;
Jatiani, Asavari ;
Mulder, Lubbertus C. F. ;
Fernandez-Sesma, Ana ;
Rutsch, Frank ;
Simon, Viviana ;
Koenig, Renate ;
Flory, Egbert .
PLOS PATHOGENS, 2011, 7 (12)
[6]
CELL-CYCLE DEPENDENCE OF FOAMY RETROVIRUS INFECTION [J].
BIENIASZ, PD ;
WEISS, RA ;
MCCLURE, MO .
JOURNAL OF VIROLOGY, 1995, 69 (11) :7295-7299
[7]
VPR IS REQUIRED FOR EFFICIENT REPLICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 IN MONONUCLEAR PHAGOCYTES [J].
CONNOR, RI ;
CHEN, BK ;
CHOE, S ;
LANDAU, NR .
VIROLOGY, 1995, 206 (02) :935-944
[8]
Demonstration that orf2 encodes the feline immunodeficiency virus transactivating (Tat) protein and characterization of a unique gene product with partial Rev activity [J].
de Parseval, A ;
Elder, JH .
JOURNAL OF VIROLOGY, 1999, 73 (01) :608-617
[9]
Macrophage tropism of HIV-1 depends on efficient cellular dNTP utilization by reverse transcriptase [J].
Diamond, TL ;
Roshal, M ;
Jamburuthugoda, VK ;
Reynolds, HM ;
Merriam, AR ;
Lee, KY ;
Balakrishnan, M ;
Bambara, RA ;
Planelles, V ;
Dewhurst, S ;
Kim, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) :51545-51553
[10]
Prototype foamy virus envelope glycoprotein leader peptide processing is mediated by a furin-like cellular protease, but cleavage is not essential for viral infectivity [J].
Duda, A ;
Stange, A ;
Lüftenegger, D ;
Stanke, N ;
Westphal, D ;
Pietschmann, T ;
Eastman, SW ;
Linial, ML ;
Rethwilm, A ;
Lindemann, D .
JOURNAL OF VIROLOGY, 2004, 78 (24) :13865-13870