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Antiviral strategies to control calicivirus infections

Caliciviridae are human or non-human pathogenic viruses with a high diversity. Some members of the Caliciviridae, i.e. human pathogenic norovirus or rabbit hemorrhagic disease virus (RHDV), are worldwide emerging pathogens. The norovirus is the major cause of viral gastroenteritis worldwide, account...

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Autores principales: Rohayem, Jacques, Bergmann, Mirko, Gebhardt, Julia, Gould, Ernest, Tucker, Paul, Mattevi, Andrea, Unge, Torsten, Hilgenfeld, Rolf, Neyts, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114105/
https://www.ncbi.nlm.nih.gov/pubmed/20471996
http://dx.doi.org/10.1016/j.antiviral.2010.05.002
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author Rohayem, Jacques
Bergmann, Mirko
Gebhardt, Julia
Gould, Ernest
Tucker, Paul
Mattevi, Andrea
Unge, Torsten
Hilgenfeld, Rolf
Neyts, Johan
author_facet Rohayem, Jacques
Bergmann, Mirko
Gebhardt, Julia
Gould, Ernest
Tucker, Paul
Mattevi, Andrea
Unge, Torsten
Hilgenfeld, Rolf
Neyts, Johan
author_sort Rohayem, Jacques
collection PubMed
description Caliciviridae are human or non-human pathogenic viruses with a high diversity. Some members of the Caliciviridae, i.e. human pathogenic norovirus or rabbit hemorrhagic disease virus (RHDV), are worldwide emerging pathogens. The norovirus is the major cause of viral gastroenteritis worldwide, accounting for about 85% of the outbreaks in Europe between 1995 and 2000. In the United States, 25 million cases of infection are reported each year. Since its emergence in 1984 as an agent of fatal hemorrhagic diseases in rabbits, RHDV has killed millions of rabbits and has been dispersed to all of the inhabitable continents. In view of their successful and apparently increasing emergence, the development of antiviral strategies to control infections due to these viral pathogens has now become an important issue in medicine and veterinary medicine. Antiviral strategies have to be based on an understanding of the epidemiology, transmission, clinical symptoms, viral replication and immunity to infection resulting from infection by these viruses. Here, we provide an overview of the mechanisms underlying calicivirus infection, focusing on the molecular aspects of replication in the host cell. Recent experimental data generated through an international collaboration on structural biology, virology and drug design within the European consortium VIZIER is also presented. Based on this analysis, we propose antiviral strategies that may significantly impact on the epidemiological characteristics of these highly successful viral pathogens.
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spelling pubmed-71141052020-04-02 Antiviral strategies to control calicivirus infections Rohayem, Jacques Bergmann, Mirko Gebhardt, Julia Gould, Ernest Tucker, Paul Mattevi, Andrea Unge, Torsten Hilgenfeld, Rolf Neyts, Johan Antiviral Res Article Caliciviridae are human or non-human pathogenic viruses with a high diversity. Some members of the Caliciviridae, i.e. human pathogenic norovirus or rabbit hemorrhagic disease virus (RHDV), are worldwide emerging pathogens. The norovirus is the major cause of viral gastroenteritis worldwide, accounting for about 85% of the outbreaks in Europe between 1995 and 2000. In the United States, 25 million cases of infection are reported each year. Since its emergence in 1984 as an agent of fatal hemorrhagic diseases in rabbits, RHDV has killed millions of rabbits and has been dispersed to all of the inhabitable continents. In view of their successful and apparently increasing emergence, the development of antiviral strategies to control infections due to these viral pathogens has now become an important issue in medicine and veterinary medicine. Antiviral strategies have to be based on an understanding of the epidemiology, transmission, clinical symptoms, viral replication and immunity to infection resulting from infection by these viruses. Here, we provide an overview of the mechanisms underlying calicivirus infection, focusing on the molecular aspects of replication in the host cell. Recent experimental data generated through an international collaboration on structural biology, virology and drug design within the European consortium VIZIER is also presented. Based on this analysis, we propose antiviral strategies that may significantly impact on the epidemiological characteristics of these highly successful viral pathogens. Elsevier B.V. 2010-08 2010-05-21 /pmc/articles/PMC7114105/ /pubmed/20471996 http://dx.doi.org/10.1016/j.antiviral.2010.05.002 Text en Copyright © 2010 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Rohayem, Jacques
Bergmann, Mirko
Gebhardt, Julia
Gould, Ernest
Tucker, Paul
Mattevi, Andrea
Unge, Torsten
Hilgenfeld, Rolf
Neyts, Johan
Antiviral strategies to control calicivirus infections
title Antiviral strategies to control calicivirus infections
title_full Antiviral strategies to control calicivirus infections
title_fullStr Antiviral strategies to control calicivirus infections
title_full_unstemmed Antiviral strategies to control calicivirus infections
title_short Antiviral strategies to control calicivirus infections
title_sort antiviral strategies to control calicivirus infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114105/
https://www.ncbi.nlm.nih.gov/pubmed/20471996
http://dx.doi.org/10.1016/j.antiviral.2010.05.002
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