» Articles » PMID: 23497255

Restriction of Diverse Retroviruses by SAMHD1

Overview
Journal Retrovirology
Publisher Biomed Central
Specialty Microbiology
Date 2013 Mar 19
PMID 23497255
Citations 99
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

A Novel Tax-Responsive Reporter T-Cell Line to Analyze Infection of HTLV-1.

Heym S, Krebs P, Ott K, Donhauser N, Kemeter L, Simon F Pathogens. 2024; 13(11).

PMID: 39599568 PMC: 11597676. DOI: 10.3390/pathogens13111015.


Unveiling the Connection: Viral Infections and Genes in dNTP Metabolism.

Lo S, Lai M, Yang C, Li H Viruses. 2024; 16(9).

PMID: 39339888 PMC: 11437409. DOI: 10.3390/v16091412.


Platform-directed allostery and quaternary structure dynamics of SAMHD1 catalysis.

Acton O, Sheppard D, Kunzelmann S, Caswell S, Nans A, Burgess A Nat Commun. 2024; 15(1):3775.

PMID: 38710701 PMC: 11074143. DOI: 10.1038/s41467-024-48237-w.


Identification and evaluation of small-molecule inhibitors against the dNTPase SAMHD1 via a comprehensive screening funnel.

Zhang S, Paulin C, Shu H, Yague-Capilla M, Michel M, Marttila P iScience. 2024; 27(2):108907.

PMID: 38318365 PMC: 10839966. DOI: 10.1016/j.isci.2024.108907.


Mechanisms of Innate Immune Sensing of HTLV-1 and Viral Immune Evasion.

Mohanty S, Harhaj E Pathogens. 2023; 12(5).

PMID: 37242405 PMC: 10221045. DOI: 10.3390/pathogens12050735.


References
1.
Goujon C, Riviere L, Jarrosson-Wuilleme L, Bernaud J, Rigal D, Darlix J . SIVSM/HIV-2 Vpx proteins promote retroviral escape from a proteasome-dependent restriction pathway present in human dendritic cells. Retrovirology. 2007; 4:2. PMC: 1779362. DOI: 10.1186/1742-4690-4-2. View

2.
Manel N, Hogstad B, Wang Y, Levy D, Unutmaz D, Littman D . A cryptic sensor for HIV-1 activates antiviral innate immunity in dendritic cells. Nature. 2010; 467(7312):214-7. PMC: 3051279. DOI: 10.1038/nature09337. View

3.
Diamond T, Roshal M, Jamburuthugoda V, Reynolds H, Merriam A, Lee K . Macrophage tropism of HIV-1 depends on efficient cellular dNTP utilization by reverse transcriptase. J Biol Chem. 2004; 279(49):51545-53. PMC: 1351161. DOI: 10.1074/jbc.M408573200. View

4.
Edwards D, Fenizia C, Gold H, de Castro-Amarante M, Buchmann C, Pise-Masison C . Orf-I and orf-II-encoded proteins in HTLV-1 infection and persistence. Viruses. 2011; 3(6):861-85. PMC: 3185781. DOI: 10.3390/v3060861. View

5.
Yu S, Baldwin D, Gwynn S, Yendapalli S, Linial M . Human foamy virus replication: a pathway distinct from that of retroviruses and hepadnaviruses. Science. 1996; 271(5255):1579-82. DOI: 10.1126/science.271.5255.1579. View