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Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics
The Paramyxoviridae genus Henipavirus is presently represented by the type species Hendra and Nipah viruses which are both recently emerged zoonotic viral pathogens responsible for repeated outbreaks associated with high morbidity and mortality in Australia, Southeast Asia, India and Bangladesh. The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315217/ https://www.ncbi.nlm.nih.gov/pubmed/22470837 http://dx.doi.org/10.3390/v4020280 |
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author | Steffen, Deborah L. Xu, Kai Nikolov, Dimitar B. Broder, Christopher C. |
author_facet | Steffen, Deborah L. Xu, Kai Nikolov, Dimitar B. Broder, Christopher C. |
author_sort | Steffen, Deborah L. |
collection | PubMed |
description | The Paramyxoviridae genus Henipavirus is presently represented by the type species Hendra and Nipah viruses which are both recently emerged zoonotic viral pathogens responsible for repeated outbreaks associated with high morbidity and mortality in Australia, Southeast Asia, India and Bangladesh. These enveloped viruses bind and enter host target cells through the coordinated activities of their attachment (G) and class I fusion (F) envelope glycoproteins. The henipavirus G glycoprotein interacts with host cellular B class ephrins, triggering conformational alterations in G that lead to the activation of the F glycoprotein, which facilitates the membrane fusion process. Using the recently published structures of HeV-G and NiV-G and other paramyxovirus glycoproteins, we review the features of the henipavirus envelope glycoproteins that appear essential for mediating the viral fusion process, including receptor binding, G-F interaction, F activation, with an emphasis on G and the mutations that disrupt viral infectivity. Finally, recent candidate therapeutics for henipavirus-mediated disease are summarized in light of their ability to inhibit HeV and NiV entry by targeting their G and F glycoproteins. |
format | Online Article Text |
id | pubmed-3315217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-33152172012-04-02 Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics Steffen, Deborah L. Xu, Kai Nikolov, Dimitar B. Broder, Christopher C. Viruses Review The Paramyxoviridae genus Henipavirus is presently represented by the type species Hendra and Nipah viruses which are both recently emerged zoonotic viral pathogens responsible for repeated outbreaks associated with high morbidity and mortality in Australia, Southeast Asia, India and Bangladesh. These enveloped viruses bind and enter host target cells through the coordinated activities of their attachment (G) and class I fusion (F) envelope glycoproteins. The henipavirus G glycoprotein interacts with host cellular B class ephrins, triggering conformational alterations in G that lead to the activation of the F glycoprotein, which facilitates the membrane fusion process. Using the recently published structures of HeV-G and NiV-G and other paramyxovirus glycoproteins, we review the features of the henipavirus envelope glycoproteins that appear essential for mediating the viral fusion process, including receptor binding, G-F interaction, F activation, with an emphasis on G and the mutations that disrupt viral infectivity. Finally, recent candidate therapeutics for henipavirus-mediated disease are summarized in light of their ability to inhibit HeV and NiV entry by targeting their G and F glycoproteins. MDPI 2012-02-13 /pmc/articles/PMC3315217/ /pubmed/22470837 http://dx.doi.org/10.3390/v4020280 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Steffen, Deborah L. Xu, Kai Nikolov, Dimitar B. Broder, Christopher C. Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics |
title | Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics |
title_full | Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics |
title_fullStr | Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics |
title_full_unstemmed | Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics |
title_short | Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics |
title_sort | henipavirus mediated membrane fusion, virus entry and targeted therapeutics |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315217/ https://www.ncbi.nlm.nih.gov/pubmed/22470837 http://dx.doi.org/10.3390/v4020280 |
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