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The activity of Nef on HIV-1 infectivity
The replication and pathogenicity of lentiviruses is crucially modulated by “auxiliary proteins” which are expressed in addition to the canonical retroviral ORFs gag, pol, and env. Strategies to inhibit the activity of such proteins are often sought and proposed as possible additions to increase eff...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033043/ https://www.ncbi.nlm.nih.gov/pubmed/24904546 http://dx.doi.org/10.3389/fmicb.2014.00232 |
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author | Basmaciogullari, Stéphane Pizzato, Massimo |
author_facet | Basmaciogullari, Stéphane Pizzato, Massimo |
author_sort | Basmaciogullari, Stéphane |
collection | PubMed |
description | The replication and pathogenicity of lentiviruses is crucially modulated by “auxiliary proteins” which are expressed in addition to the canonical retroviral ORFs gag, pol, and env. Strategies to inhibit the activity of such proteins are often sought and proposed as possible additions to increase efficacy of the traditional antiretroviral therapy. This requires the acquisition of an in-depth knowledge of the molecular mechanisms underlying their function. The Nef auxiliary protein is expressed uniquely by primate lentiviruses and plays an important role in virus replication in vivo and in the onset of AIDS. Among its several activities Nef enhances the intrinsic infectivity of progeny virions through a mechanism which remains today enigmatic. Here we review the current knowledge surrounding such activity and we discuss its possible role in HIV biology. |
format | Online Article Text |
id | pubmed-4033043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40330432014-06-05 The activity of Nef on HIV-1 infectivity Basmaciogullari, Stéphane Pizzato, Massimo Front Microbiol Microbiology The replication and pathogenicity of lentiviruses is crucially modulated by “auxiliary proteins” which are expressed in addition to the canonical retroviral ORFs gag, pol, and env. Strategies to inhibit the activity of such proteins are often sought and proposed as possible additions to increase efficacy of the traditional antiretroviral therapy. This requires the acquisition of an in-depth knowledge of the molecular mechanisms underlying their function. The Nef auxiliary protein is expressed uniquely by primate lentiviruses and plays an important role in virus replication in vivo and in the onset of AIDS. Among its several activities Nef enhances the intrinsic infectivity of progeny virions through a mechanism which remains today enigmatic. Here we review the current knowledge surrounding such activity and we discuss its possible role in HIV biology. Frontiers Media S.A. 2014-05-20 /pmc/articles/PMC4033043/ /pubmed/24904546 http://dx.doi.org/10.3389/fmicb.2014.00232 Text en Copyright © 2014 Basmaciogullari and Pizzato. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Basmaciogullari, Stéphane Pizzato, Massimo The activity of Nef on HIV-1 infectivity |
title | The activity of Nef on HIV-1 infectivity |
title_full | The activity of Nef on HIV-1 infectivity |
title_fullStr | The activity of Nef on HIV-1 infectivity |
title_full_unstemmed | The activity of Nef on HIV-1 infectivity |
title_short | The activity of Nef on HIV-1 infectivity |
title_sort | activity of nef on hiv-1 infectivity |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033043/ https://www.ncbi.nlm.nih.gov/pubmed/24904546 http://dx.doi.org/10.3389/fmicb.2014.00232 |
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