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Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes

Hepatitis E virus (HEV) has received relatively little attention for decades although it is now considered as one of the most frequent causes of acute hepatitis worldwide. Our knowledge of this enterically-transmitted, positive-strand RNA virus and its life cycle remains scarce but research on HEV h...

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Autores principales: Oechslin, Noémie, Ankavay, Maliki, Moradpour, Darius, Gouttenoire, Jérôme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147066/
https://www.ncbi.nlm.nih.gov/pubmed/37112849
http://dx.doi.org/10.3390/v15040869
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author Oechslin, Noémie
Ankavay, Maliki
Moradpour, Darius
Gouttenoire, Jérôme
author_facet Oechslin, Noémie
Ankavay, Maliki
Moradpour, Darius
Gouttenoire, Jérôme
author_sort Oechslin, Noémie
collection PubMed
description Hepatitis E virus (HEV) has received relatively little attention for decades although it is now considered as one of the most frequent causes of acute hepatitis worldwide. Our knowledge of this enterically-transmitted, positive-strand RNA virus and its life cycle remains scarce but research on HEV has gained momentum more recently. Indeed, advances in the molecular virology of hepatitis E, including the establishment of subgenomic replicons and infectious molecular clones, now allow study of the entire viral life cycle and to explore host factors required for productive infection. Here, we provide an overview on currently available systems, with an emphasis on selectable replicons and recombinant reporter genomes. Furthermore, we discuss the challenges in developing new systems which should enable to further investigate this widely distributed and important pathogen.
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spelling pubmed-101470662023-04-29 Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes Oechslin, Noémie Ankavay, Maliki Moradpour, Darius Gouttenoire, Jérôme Viruses Review Hepatitis E virus (HEV) has received relatively little attention for decades although it is now considered as one of the most frequent causes of acute hepatitis worldwide. Our knowledge of this enterically-transmitted, positive-strand RNA virus and its life cycle remains scarce but research on HEV has gained momentum more recently. Indeed, advances in the molecular virology of hepatitis E, including the establishment of subgenomic replicons and infectious molecular clones, now allow study of the entire viral life cycle and to explore host factors required for productive infection. Here, we provide an overview on currently available systems, with an emphasis on selectable replicons and recombinant reporter genomes. Furthermore, we discuss the challenges in developing new systems which should enable to further investigate this widely distributed and important pathogen. MDPI 2023-03-28 /pmc/articles/PMC10147066/ /pubmed/37112849 http://dx.doi.org/10.3390/v15040869 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Oechslin, Noémie
Ankavay, Maliki
Moradpour, Darius
Gouttenoire, Jérôme
Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes
title Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes
title_full Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes
title_fullStr Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes
title_full_unstemmed Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes
title_short Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes
title_sort expanding the hepatitis e virus toolbox: selectable replicons and recombinant reporter genomes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147066/
https://www.ncbi.nlm.nih.gov/pubmed/37112849
http://dx.doi.org/10.3390/v15040869
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