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The Great Escape: Viral Strategies to Counter BST-2/Tetherin

The interferon-induced BST-2 protein has the unique ability to restrict the egress of HIV-1, Kaposi's sarcoma–associated herpesvirus (KSHV), Ebola virus, and other enveloped viruses. The observation that virions remain attached to the surface of BST-2-expressing cells led to the renaming of BST...

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Autores principales: Douglas, Janet L., Gustin, Jean K., Viswanathan, Kasinath, Mansouri, Mandana, Moses, Ashlee V., Früh, Klaus
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869331/
https://www.ncbi.nlm.nih.gov/pubmed/20485522
http://dx.doi.org/10.1371/journal.ppat.1000913
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author Douglas, Janet L.
Gustin, Jean K.
Viswanathan, Kasinath
Mansouri, Mandana
Moses, Ashlee V.
Früh, Klaus
author_facet Douglas, Janet L.
Gustin, Jean K.
Viswanathan, Kasinath
Mansouri, Mandana
Moses, Ashlee V.
Früh, Klaus
author_sort Douglas, Janet L.
collection PubMed
description The interferon-induced BST-2 protein has the unique ability to restrict the egress of HIV-1, Kaposi's sarcoma–associated herpesvirus (KSHV), Ebola virus, and other enveloped viruses. The observation that virions remain attached to the surface of BST-2-expressing cells led to the renaming of BST-2 as “tetherin”. However, viral proteins such as HIV-1 Vpu, simian immunodeficiency virus Nef, and KSHV K5 counteract BST-2, thereby allowing mature virions to readily escape from infected cells. Since the anti-viral function of BST-2 was discovered, there has been an explosion of research into several aspects of this intriguing interplay between host and virus. This review focuses on recent work addressing the molecular mechanisms involved in BST-2 restriction of viral egress and the species-specific countermeasures employed by various viruses.
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spelling pubmed-28693312010-05-19 The Great Escape: Viral Strategies to Counter BST-2/Tetherin Douglas, Janet L. Gustin, Jean K. Viswanathan, Kasinath Mansouri, Mandana Moses, Ashlee V. Früh, Klaus PLoS Pathog Review The interferon-induced BST-2 protein has the unique ability to restrict the egress of HIV-1, Kaposi's sarcoma–associated herpesvirus (KSHV), Ebola virus, and other enveloped viruses. The observation that virions remain attached to the surface of BST-2-expressing cells led to the renaming of BST-2 as “tetherin”. However, viral proteins such as HIV-1 Vpu, simian immunodeficiency virus Nef, and KSHV K5 counteract BST-2, thereby allowing mature virions to readily escape from infected cells. Since the anti-viral function of BST-2 was discovered, there has been an explosion of research into several aspects of this intriguing interplay between host and virus. This review focuses on recent work addressing the molecular mechanisms involved in BST-2 restriction of viral egress and the species-specific countermeasures employed by various viruses. Public Library of Science 2010-05-13 /pmc/articles/PMC2869331/ /pubmed/20485522 http://dx.doi.org/10.1371/journal.ppat.1000913 Text en Douglas et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Review
Douglas, Janet L.
Gustin, Jean K.
Viswanathan, Kasinath
Mansouri, Mandana
Moses, Ashlee V.
Früh, Klaus
The Great Escape: Viral Strategies to Counter BST-2/Tetherin
title The Great Escape: Viral Strategies to Counter BST-2/Tetherin
title_full The Great Escape: Viral Strategies to Counter BST-2/Tetherin
title_fullStr The Great Escape: Viral Strategies to Counter BST-2/Tetherin
title_full_unstemmed The Great Escape: Viral Strategies to Counter BST-2/Tetherin
title_short The Great Escape: Viral Strategies to Counter BST-2/Tetherin
title_sort great escape: viral strategies to counter bst-2/tetherin
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869331/
https://www.ncbi.nlm.nih.gov/pubmed/20485522
http://dx.doi.org/10.1371/journal.ppat.1000913
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