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Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses
Noroviruses belong to the Caliciviridae family of single-stranded positive-sense RNA viruses. The genus Norovirus includes seven genogroups (designated GI-GVII), of which GI, GII and GIV infect humans. Human noroviruses are responsible for widespread outbreaks of acute gastroenteritis and represent...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114559/ https://www.ncbi.nlm.nih.gov/pubmed/28041960 http://dx.doi.org/10.1016/j.virusres.2016.12.018 |
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author | Deval, Jerome Jin, Zhinan Chuang, Ying-Chih Kao, C. Cheng |
author_facet | Deval, Jerome Jin, Zhinan Chuang, Ying-Chih Kao, C. Cheng |
author_sort | Deval, Jerome |
collection | PubMed |
description | Noroviruses belong to the Caliciviridae family of single-stranded positive-sense RNA viruses. The genus Norovirus includes seven genogroups (designated GI-GVII), of which GI, GII and GIV infect humans. Human noroviruses are responsible for widespread outbreaks of acute gastroenteritis and represent one of the most common causes of foodborne illness. No vaccine or antiviral treatment options are available for norovirus infection. The RNA-dependent RNA polymerase (RdRp) of noroviruses is a key enzyme responsible for transcription and replication of the viral genome. Here, we review the progress made in understanding the structures and functions of norovirus RdRp and its use as a target for small molecule inhibitors. Crystal structures of the RdRp at different stages of substrate interaction have been determined, which shed light on its multi-step catalytic cycle. The in vitro assays and in vivo animal models that have been developed to identify and characterize inhibitors of norovirus RdRp are also summarized, followed by an update on the current antiviral research targeting different regions of norovirus RdRp. In the future, structure-based drug design and rational optimization of known nucleoside and non-nucleoside inhibitors of norovirus RdRp may pave the way towards the next generation of direct-acting antivirals. |
format | Online Article Text |
id | pubmed-7114559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71145592020-04-02 Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses Deval, Jerome Jin, Zhinan Chuang, Ying-Chih Kao, C. Cheng Virus Res Article Noroviruses belong to the Caliciviridae family of single-stranded positive-sense RNA viruses. The genus Norovirus includes seven genogroups (designated GI-GVII), of which GI, GII and GIV infect humans. Human noroviruses are responsible for widespread outbreaks of acute gastroenteritis and represent one of the most common causes of foodborne illness. No vaccine or antiviral treatment options are available for norovirus infection. The RNA-dependent RNA polymerase (RdRp) of noroviruses is a key enzyme responsible for transcription and replication of the viral genome. Here, we review the progress made in understanding the structures and functions of norovirus RdRp and its use as a target for small molecule inhibitors. Crystal structures of the RdRp at different stages of substrate interaction have been determined, which shed light on its multi-step catalytic cycle. The in vitro assays and in vivo animal models that have been developed to identify and characterize inhibitors of norovirus RdRp are also summarized, followed by an update on the current antiviral research targeting different regions of norovirus RdRp. In the future, structure-based drug design and rational optimization of known nucleoside and non-nucleoside inhibitors of norovirus RdRp may pave the way towards the next generation of direct-acting antivirals. Published by Elsevier B.V. 2017-04-15 2016-12-29 /pmc/articles/PMC7114559/ /pubmed/28041960 http://dx.doi.org/10.1016/j.virusres.2016.12.018 Text en © 2016 Published by Elsevier B.V. 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 Deval, Jerome Jin, Zhinan Chuang, Ying-Chih Kao, C. Cheng Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses |
title | Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses |
title_full | Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses |
title_fullStr | Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses |
title_full_unstemmed | Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses |
title_short | Structure(s), function(s), and inhibition of the RNA-dependent RNA polymerase of noroviruses |
title_sort | structure(s), function(s), and inhibition of the rna-dependent rna polymerase of noroviruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114559/ https://www.ncbi.nlm.nih.gov/pubmed/28041960 http://dx.doi.org/10.1016/j.virusres.2016.12.018 |
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