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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...

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Autores principales: 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
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
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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.
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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
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