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An essential RNA element resides in a central region of hepatitis E virus ORF2

Hepatitis E virus (genus Hepevirus, family Hepeviridae) is one of the most important causes of acute hepatitis in adults, particularly among pregnant women, throughout Asia and Africa where mortality rates can be 20–30 %. Hepatitis E virus has a single-stranded positive-sense RNA genome that contain...

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Autores principales: Emerson, Suzanne U., Nguyen, Hanh T., Torian, Udana, Mather, Karly, Firth, Andrew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for General Microbiology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709636/
https://www.ncbi.nlm.nih.gov/pubmed/23515023
http://dx.doi.org/10.1099/vir.0.051870-0
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author Emerson, Suzanne U.
Nguyen, Hanh T.
Torian, Udana
Mather, Karly
Firth, Andrew E.
author_facet Emerson, Suzanne U.
Nguyen, Hanh T.
Torian, Udana
Mather, Karly
Firth, Andrew E.
author_sort Emerson, Suzanne U.
collection PubMed
description Hepatitis E virus (genus Hepevirus, family Hepeviridae) is one of the most important causes of acute hepatitis in adults, particularly among pregnant women, throughout Asia and Africa where mortality rates can be 20–30 %. Hepatitis E virus has a single-stranded positive-sense RNA genome that contains three translated ORFs. The two 3′ ORFs are translated from a subgenomic RNA. Functional RNA elements have been identified in and adjacent to the genomic 5′ and 3′ UTRs and in and around the intergenic region. Here we describe an additional RNA element that is located in a central region of ORF2. The RNA element is predicted to fold into two highly conserved stem–loop structures, ISL1 and ISL2. Mutations that disrupt the predicted structures, without altering the encoded amino acid sequence, result in a drastic reduction in capsid protein synthesis. This indicates that the RNA element plays an important role in one of the early steps of virus replication. The structures were further investigated using a replicon that expresses Gaussia luciferase in place of the capsid protein. Single mutations in ISL2 severely reduced luciferase expression, but a pair of compensatory mutations that were predicted to restore the ISL2 structure, restored luciferase expression to near-WT levels, thus lending experimental support to the predicted structure. Nonetheless the precise role of the ISL1+ISL2 element remains unknown.
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spelling pubmed-37096362013-07-24 An essential RNA element resides in a central region of hepatitis E virus ORF2 Emerson, Suzanne U. Nguyen, Hanh T. Torian, Udana Mather, Karly Firth, Andrew E. J Gen Virol Animal Hepatitis E virus (genus Hepevirus, family Hepeviridae) is one of the most important causes of acute hepatitis in adults, particularly among pregnant women, throughout Asia and Africa where mortality rates can be 20–30 %. Hepatitis E virus has a single-stranded positive-sense RNA genome that contains three translated ORFs. The two 3′ ORFs are translated from a subgenomic RNA. Functional RNA elements have been identified in and adjacent to the genomic 5′ and 3′ UTRs and in and around the intergenic region. Here we describe an additional RNA element that is located in a central region of ORF2. The RNA element is predicted to fold into two highly conserved stem–loop structures, ISL1 and ISL2. Mutations that disrupt the predicted structures, without altering the encoded amino acid sequence, result in a drastic reduction in capsid protein synthesis. This indicates that the RNA element plays an important role in one of the early steps of virus replication. The structures were further investigated using a replicon that expresses Gaussia luciferase in place of the capsid protein. Single mutations in ISL2 severely reduced luciferase expression, but a pair of compensatory mutations that were predicted to restore the ISL2 structure, restored luciferase expression to near-WT levels, thus lending experimental support to the predicted structure. Nonetheless the precise role of the ISL1+ISL2 element remains unknown. Society for General Microbiology 2013-07 /pmc/articles/PMC3709636/ /pubmed/23515023 http://dx.doi.org/10.1099/vir.0.051870-0 Text en © 2013 SGM http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Animal
Emerson, Suzanne U.
Nguyen, Hanh T.
Torian, Udana
Mather, Karly
Firth, Andrew E.
An essential RNA element resides in a central region of hepatitis E virus ORF2
title An essential RNA element resides in a central region of hepatitis E virus ORF2
title_full An essential RNA element resides in a central region of hepatitis E virus ORF2
title_fullStr An essential RNA element resides in a central region of hepatitis E virus ORF2
title_full_unstemmed An essential RNA element resides in a central region of hepatitis E virus ORF2
title_short An essential RNA element resides in a central region of hepatitis E virus ORF2
title_sort essential rna element resides in a central region of hepatitis e virus orf2
topic Animal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709636/
https://www.ncbi.nlm.nih.gov/pubmed/23515023
http://dx.doi.org/10.1099/vir.0.051870-0
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