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Restriction of diverse retroviruses by SAMHD1
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 transcript...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605129/ https://www.ncbi.nlm.nih.gov/pubmed/23497255 http://dx.doi.org/10.1186/1742-4690-10-26 |
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author | Gramberg, Thomas Kahle, Tanja Bloch, Nicolin Wittmann, Sabine Müllers, Erik Daddacha, Waaqo Hofmann, Henning Kim, Baek Lindemann, Dirk Landau, Nathaniel R |
author_facet | Gramberg, Thomas Kahle, Tanja Bloch, Nicolin Wittmann, Sabine Müllers, Erik Daddacha, Waaqo Hofmann, Henning Kim, Baek Lindemann, Dirk Landau, Nathaniel R |
author_sort | Gramberg, Thomas |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3605129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36051292013-03-22 Restriction of diverse retroviruses by SAMHD1 Gramberg, Thomas Kahle, Tanja Bloch, Nicolin Wittmann, Sabine Müllers, Erik Daddacha, Waaqo Hofmann, Henning Kim, Baek Lindemann, Dirk Landau, Nathaniel R Retrovirology Research 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. BioMed Central 2013-03-05 /pmc/articles/PMC3605129/ /pubmed/23497255 http://dx.doi.org/10.1186/1742-4690-10-26 Text en Copyright ©2013 Gramberg et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Gramberg, Thomas Kahle, Tanja Bloch, Nicolin Wittmann, Sabine Müllers, Erik Daddacha, Waaqo Hofmann, Henning Kim, Baek Lindemann, Dirk Landau, Nathaniel R Restriction of diverse retroviruses by SAMHD1 |
title | Restriction of diverse retroviruses by SAMHD1 |
title_full | Restriction of diverse retroviruses by SAMHD1 |
title_fullStr | Restriction of diverse retroviruses by SAMHD1 |
title_full_unstemmed | Restriction of diverse retroviruses by SAMHD1 |
title_short | Restriction of diverse retroviruses by SAMHD1 |
title_sort | restriction of diverse retroviruses by samhd1 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605129/ https://www.ncbi.nlm.nih.gov/pubmed/23497255 http://dx.doi.org/10.1186/1742-4690-10-26 |
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