Cargando…
Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program
Herpesvirus infection initiates a range of perturbations in the host cell, which remain poorly understood at the level of individual cells. Here, we quantify the transcriptome of single human primary fibroblasts during the first hours of lytic infection with HSV-1. By applying a generalizable analys...
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/PMC6814756/ https://www.ncbi.nlm.nih.gov/pubmed/31653857 http://dx.doi.org/10.1038/s41467-019-12894-z |
_version_ | 1783463048606908416 |
---|---|
author | Wyler, Emanuel Franke, Vedran Menegatti, Jennifer Kocks, Christine Boltengagen, Anastasiya Praktiknjo, Samantha Walch-Rückheim, Barbara Bosse, Jens Rajewsky, Nikolaus Grässer, Friedrich Akalin, Altuna Landthaler, Markus |
author_facet | Wyler, Emanuel Franke, Vedran Menegatti, Jennifer Kocks, Christine Boltengagen, Anastasiya Praktiknjo, Samantha Walch-Rückheim, Barbara Bosse, Jens Rajewsky, Nikolaus Grässer, Friedrich Akalin, Altuna Landthaler, Markus |
author_sort | Wyler, Emanuel |
collection | PubMed |
description | Herpesvirus infection initiates a range of perturbations in the host cell, which remain poorly understood at the level of individual cells. Here, we quantify the transcriptome of single human primary fibroblasts during the first hours of lytic infection with HSV-1. By applying a generalizable analysis scheme, we define a precise temporal order of early viral gene expression and propose a set-wise emergence of viral genes. We identify host cell genes and pathways relevant for infection by combining three different computational approaches: gene and pathway overdispersion analysis, prediction of cell-state transition probabilities, as well as future cell states. One transcriptional program, which correlates with increased resistance to infection, implicates the transcription factor NRF2. Consequently, Bardoxolone methyl and Sulforaphane, two known NRF2 agonists, impair virus production, suggesting that NRF2 activation restricts viral infection. Our study provides insights into early stages of HSV-1 infection and serves as a general blueprint for the investigation of heterogeneous cell states in virus infection. |
format | Online Article Text |
id | pubmed-6814756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68147562019-10-28 Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program Wyler, Emanuel Franke, Vedran Menegatti, Jennifer Kocks, Christine Boltengagen, Anastasiya Praktiknjo, Samantha Walch-Rückheim, Barbara Bosse, Jens Rajewsky, Nikolaus Grässer, Friedrich Akalin, Altuna Landthaler, Markus Nat Commun Article Herpesvirus infection initiates a range of perturbations in the host cell, which remain poorly understood at the level of individual cells. Here, we quantify the transcriptome of single human primary fibroblasts during the first hours of lytic infection with HSV-1. By applying a generalizable analysis scheme, we define a precise temporal order of early viral gene expression and propose a set-wise emergence of viral genes. We identify host cell genes and pathways relevant for infection by combining three different computational approaches: gene and pathway overdispersion analysis, prediction of cell-state transition probabilities, as well as future cell states. One transcriptional program, which correlates with increased resistance to infection, implicates the transcription factor NRF2. Consequently, Bardoxolone methyl and Sulforaphane, two known NRF2 agonists, impair virus production, suggesting that NRF2 activation restricts viral infection. Our study provides insights into early stages of HSV-1 infection and serves as a general blueprint for the investigation of heterogeneous cell states in virus infection. Nature Publishing Group UK 2019-10-25 /pmc/articles/PMC6814756/ /pubmed/31653857 http://dx.doi.org/10.1038/s41467-019-12894-z 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 Wyler, Emanuel Franke, Vedran Menegatti, Jennifer Kocks, Christine Boltengagen, Anastasiya Praktiknjo, Samantha Walch-Rückheim, Barbara Bosse, Jens Rajewsky, Nikolaus Grässer, Friedrich Akalin, Altuna Landthaler, Markus Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program |
title | Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program |
title_full | Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program |
title_fullStr | Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program |
title_full_unstemmed | Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program |
title_short | Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program |
title_sort | single-cell rna-sequencing of herpes simplex virus 1-infected cells connects nrf2 activation to an antiviral program |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814756/ https://www.ncbi.nlm.nih.gov/pubmed/31653857 http://dx.doi.org/10.1038/s41467-019-12894-z |
work_keys_str_mv | AT wyleremanuel singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT frankevedran singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT menegattijennifer singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT kockschristine singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT boltengagenanastasiya singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT praktiknjosamantha singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT walchruckheimbarbara singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT bossejens singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT rajewskynikolaus singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT grasserfriedrich singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT akalinaltuna singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram AT landthalermarkus singlecellrnasequencingofherpessimplexvirus1infectedcellsconnectsnrf2activationtoanantiviralprogram |