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Crabohydrate-Related Inhibitors of Dengue Virus Entry

Dengue virus (DENV), which is transmitted by Aedes mosquitoes, causes fever and hemorrhagic disorders in humans. The virus entry process mediated through host receptor molecule(s) is crucial for virus propagation and the pathological progression of dengue disease. Therefore, elucidation of the molec...

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Autores principales: Hidari, Kazuya I.P.J., Abe, Tomoko, Suzuki, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640517/
https://www.ncbi.nlm.nih.gov/pubmed/23389466
http://dx.doi.org/10.3390/v5020605
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author Hidari, Kazuya I.P.J.
Abe, Tomoko
Suzuki, Takashi
author_facet Hidari, Kazuya I.P.J.
Abe, Tomoko
Suzuki, Takashi
author_sort Hidari, Kazuya I.P.J.
collection PubMed
description Dengue virus (DENV), which is transmitted by Aedes mosquitoes, causes fever and hemorrhagic disorders in humans. The virus entry process mediated through host receptor molecule(s) is crucial for virus propagation and the pathological progression of dengue disease. Therefore, elucidation of the molecular mechanisms underlying virus entry is essential for an understanding of dengue pathology and for the development of effective new anti-dengue agents. DENV binds to its receptor molecules mediated through a viral envelope (E) protein, followed by incorporation of the virus-receptor complex inside cells. The fusion between incorporated virus particles and host endosome membrane under acidic conditions is mediated through the function of DENV E protein. Carbohydrate molecules, such as sulfated glycosaminoglycans (GAG) and glycosphingolipids, and carbohydrate-recognition proteins, termed lectins, inhibit virus entry. This review focuses on carbohydrate-derived entry inhibitors, and also introduces functionally related compounds with similar inhibitory mechanisms against DENV entry.
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spelling pubmed-36405172013-05-03 Crabohydrate-Related Inhibitors of Dengue Virus Entry Hidari, Kazuya I.P.J. Abe, Tomoko Suzuki, Takashi Viruses Review Dengue virus (DENV), which is transmitted by Aedes mosquitoes, causes fever and hemorrhagic disorders in humans. The virus entry process mediated through host receptor molecule(s) is crucial for virus propagation and the pathological progression of dengue disease. Therefore, elucidation of the molecular mechanisms underlying virus entry is essential for an understanding of dengue pathology and for the development of effective new anti-dengue agents. DENV binds to its receptor molecules mediated through a viral envelope (E) protein, followed by incorporation of the virus-receptor complex inside cells. The fusion between incorporated virus particles and host endosome membrane under acidic conditions is mediated through the function of DENV E protein. Carbohydrate molecules, such as sulfated glycosaminoglycans (GAG) and glycosphingolipids, and carbohydrate-recognition proteins, termed lectins, inhibit virus entry. This review focuses on carbohydrate-derived entry inhibitors, and also introduces functionally related compounds with similar inhibitory mechanisms against DENV entry. MDPI 2013-02-06 /pmc/articles/PMC3640517/ /pubmed/23389466 http://dx.doi.org/10.3390/v5020605 Text en © 2013 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
Hidari, Kazuya I.P.J.
Abe, Tomoko
Suzuki, Takashi
Crabohydrate-Related Inhibitors of Dengue Virus Entry
title Crabohydrate-Related Inhibitors of Dengue Virus Entry
title_full Crabohydrate-Related Inhibitors of Dengue Virus Entry
title_fullStr Crabohydrate-Related Inhibitors of Dengue Virus Entry
title_full_unstemmed Crabohydrate-Related Inhibitors of Dengue Virus Entry
title_short Crabohydrate-Related Inhibitors of Dengue Virus Entry
title_sort crabohydrate-related inhibitors of dengue virus entry
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640517/
https://www.ncbi.nlm.nih.gov/pubmed/23389466
http://dx.doi.org/10.3390/v5020605
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