The transcriptional and translational landscape of HCoV-OC43 infection.
The coronavirus HCoV-OC43 circulates continuously in the human population and is a frequent cause of the common cold. Here, we generated a high-resolution atlas of the transcriptional and translational landscape of OC43 during a time course following infection of human lung fibroblasts. Using riboso...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2025-01-01
|
Series: | PLoS Pathogens |
Online Access: | https://doi.org/10.1371/journal.ppat.1012831 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832540350352195584 |
---|---|
author | Stefan Bresson Emanuela Sani Alicja Armatowska Charles Dixon David Tollervey |
author_facet | Stefan Bresson Emanuela Sani Alicja Armatowska Charles Dixon David Tollervey |
author_sort | Stefan Bresson |
collection | DOAJ |
description | The coronavirus HCoV-OC43 circulates continuously in the human population and is a frequent cause of the common cold. Here, we generated a high-resolution atlas of the transcriptional and translational landscape of OC43 during a time course following infection of human lung fibroblasts. Using ribosome profiling, we quantified the relative expression of the canonical open reading frames (ORFs) and identified previously unannotated ORFs. These included several potential short upstream ORFs and a putative ORF nested inside the M gene. In parallel, we analyzed the cellular response to infection. Endoplasmic reticulum (ER) stress response genes were transcriptionally and translationally induced beginning 12 and 18 hours post infection, respectively. By contrast, conventional antiviral genes mostly remained quiescent. At the same time points, we observed accumulation and increased translation of noncoding transcripts normally targeted by nonsense mediated decay (NMD), suggesting NMD is suppressed during the course of infection. This work provides resources for deeper understanding of OC43 gene expression and the cellular responses during infection. |
format | Article |
id | doaj-art-c9617e6907884978b73defe3689d743f |
institution | Kabale University |
issn | 1553-7366 1553-7374 |
language | English |
publishDate | 2025-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS Pathogens |
spelling | doaj-art-c9617e6907884978b73defe3689d743f2025-02-05T05:30:52ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742025-01-01211e101283110.1371/journal.ppat.1012831The transcriptional and translational landscape of HCoV-OC43 infection.Stefan BressonEmanuela SaniAlicja ArmatowskaCharles DixonDavid TollerveyThe coronavirus HCoV-OC43 circulates continuously in the human population and is a frequent cause of the common cold. Here, we generated a high-resolution atlas of the transcriptional and translational landscape of OC43 during a time course following infection of human lung fibroblasts. Using ribosome profiling, we quantified the relative expression of the canonical open reading frames (ORFs) and identified previously unannotated ORFs. These included several potential short upstream ORFs and a putative ORF nested inside the M gene. In parallel, we analyzed the cellular response to infection. Endoplasmic reticulum (ER) stress response genes were transcriptionally and translationally induced beginning 12 and 18 hours post infection, respectively. By contrast, conventional antiviral genes mostly remained quiescent. At the same time points, we observed accumulation and increased translation of noncoding transcripts normally targeted by nonsense mediated decay (NMD), suggesting NMD is suppressed during the course of infection. This work provides resources for deeper understanding of OC43 gene expression and the cellular responses during infection.https://doi.org/10.1371/journal.ppat.1012831 |
spellingShingle | Stefan Bresson Emanuela Sani Alicja Armatowska Charles Dixon David Tollervey The transcriptional and translational landscape of HCoV-OC43 infection. PLoS Pathogens |
title | The transcriptional and translational landscape of HCoV-OC43 infection. |
title_full | The transcriptional and translational landscape of HCoV-OC43 infection. |
title_fullStr | The transcriptional and translational landscape of HCoV-OC43 infection. |
title_full_unstemmed | The transcriptional and translational landscape of HCoV-OC43 infection. |
title_short | The transcriptional and translational landscape of HCoV-OC43 infection. |
title_sort | transcriptional and translational landscape of hcov oc43 infection |
url | https://doi.org/10.1371/journal.ppat.1012831 |
work_keys_str_mv | AT stefanbresson thetranscriptionalandtranslationallandscapeofhcovoc43infection AT emanuelasani thetranscriptionalandtranslationallandscapeofhcovoc43infection AT alicjaarmatowska thetranscriptionalandtranslationallandscapeofhcovoc43infection AT charlesdixon thetranscriptionalandtranslationallandscapeofhcovoc43infection AT davidtollervey thetranscriptionalandtranslationallandscapeofhcovoc43infection AT stefanbresson transcriptionalandtranslationallandscapeofhcovoc43infection AT emanuelasani transcriptionalandtranslationallandscapeofhcovoc43infection AT alicjaarmatowska transcriptionalandtranslationallandscapeofhcovoc43infection AT charlesdixon transcriptionalandtranslationallandscapeofhcovoc43infection AT davidtollervey transcriptionalandtranslationallandscapeofhcovoc43infection |