Cargando…
A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells
Human enteroviruses (HEVs) of the family Picornaviridae, which comprises non-enveloped RNA viruses, are ubiquitous worldwide. The majority of EV proteins are derived from viral polyproteins encoded by a single open reading frame (ORF). Here, we characterize a second ORF in HEVs that is crucial for v...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731315/ https://www.ncbi.nlm.nih.gov/pubmed/31492846 http://dx.doi.org/10.1038/s41467-019-12040-9 |
_version_ | 1783449666454552576 |
---|---|
author | Guo, Haoran Li, Yan Liu, Guanchen Jiang, Yunhe Shen, Siyu Bi, Ran Huang, Honglan Cheng, Tong Wang, Chunxi Wei, Wei |
author_facet | Guo, Haoran Li, Yan Liu, Guanchen Jiang, Yunhe Shen, Siyu Bi, Ran Huang, Honglan Cheng, Tong Wang, Chunxi Wei, Wei |
author_sort | Guo, Haoran |
collection | PubMed |
description | Human enteroviruses (HEVs) of the family Picornaviridae, which comprises non-enveloped RNA viruses, are ubiquitous worldwide. The majority of EV proteins are derived from viral polyproteins encoded by a single open reading frame (ORF). Here, we characterize a second ORF in HEVs that is crucial for viral intestinal infection. Disruption of ORF2p expression decreases the replication capacity of EV-A71 in human intestinal epithelial cells (IECs). Ectopic expression of ORF2p proteins derived from diverse enteric enteroviruses sensitizes intestinal cells to the replication of ORF2p-defective EV-A71 and respiratory enterovirus EV-D68. We show that the highly conserved WIGHPV domain of ORF2p is important for ORF2p-dependent viral intestinal infection. ORF2p expression is required for EV-A71 particle release from IECs and can support productive EV-D68 infection in IECs by facilitating virus release. Our results indicate that ORF2p is a determining factor for enteric enterovirus replication in IECs. |
format | Online Article Text |
id | pubmed-6731315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67313152019-09-09 A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells Guo, Haoran Li, Yan Liu, Guanchen Jiang, Yunhe Shen, Siyu Bi, Ran Huang, Honglan Cheng, Tong Wang, Chunxi Wei, Wei Nat Commun Article Human enteroviruses (HEVs) of the family Picornaviridae, which comprises non-enveloped RNA viruses, are ubiquitous worldwide. The majority of EV proteins are derived from viral polyproteins encoded by a single open reading frame (ORF). Here, we characterize a second ORF in HEVs that is crucial for viral intestinal infection. Disruption of ORF2p expression decreases the replication capacity of EV-A71 in human intestinal epithelial cells (IECs). Ectopic expression of ORF2p proteins derived from diverse enteric enteroviruses sensitizes intestinal cells to the replication of ORF2p-defective EV-A71 and respiratory enterovirus EV-D68. We show that the highly conserved WIGHPV domain of ORF2p is important for ORF2p-dependent viral intestinal infection. ORF2p expression is required for EV-A71 particle release from IECs and can support productive EV-D68 infection in IECs by facilitating virus release. Our results indicate that ORF2p is a determining factor for enteric enterovirus replication in IECs. Nature Publishing Group UK 2019-09-06 /pmc/articles/PMC6731315/ /pubmed/31492846 http://dx.doi.org/10.1038/s41467-019-12040-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guo, Haoran Li, Yan Liu, Guanchen Jiang, Yunhe Shen, Siyu Bi, Ran Huang, Honglan Cheng, Tong Wang, Chunxi Wei, Wei A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells |
title | A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells |
title_full | A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells |
title_fullStr | A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells |
title_full_unstemmed | A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells |
title_short | A second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells |
title_sort | second open reading frame in human enterovirus determines viral replication in intestinal epithelial cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731315/ https://www.ncbi.nlm.nih.gov/pubmed/31492846 http://dx.doi.org/10.1038/s41467-019-12040-9 |
work_keys_str_mv | AT guohaoran asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT liyan asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT liuguanchen asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT jiangyunhe asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT shensiyu asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT biran asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT huanghonglan asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT chengtong asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT wangchunxi asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT weiwei asecondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT guohaoran secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT liyan secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT liuguanchen secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT jiangyunhe secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT shensiyu secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT biran secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT huanghonglan secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT chengtong secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT wangchunxi secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells AT weiwei secondopenreadingframeinhumanenterovirusdeterminesviralreplicationinintestinalepithelialcells |