Cargando…

Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity

Patients with chronic lung disease (CLD) have an increased risk for severe coronavirus disease-19 (COVID-19) and poor outcomes. Here, we analyze the transcriptomes of 611,398 single cells isolated from healthy and CLD lungs to identify molecular characteristics of lung cells that may account for wor...

Descripción completa

Detalles Bibliográficos
Autores principales: Bui, Linh T., Winters, Nichelle I., Chung, Mei-I, Joseph, Chitra, Gutierrez, Austin J., Habermann, Arun C., Adams, Taylor S., Schupp, Jonas C., Poli, Sergio, Peter, Lance M., Taylor, Chase J., Blackburn, Jessica B., Richmond, Bradley W., Nicholson, Andrew G., Rassl, Doris, Wallace, William A., Rosas, Ivan O., Jenkins, R. Gisli, Kaminski, Naftali, Kropski, Jonathan A., Banovich, Nicholas E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280215/
https://www.ncbi.nlm.nih.gov/pubmed/34262047
http://dx.doi.org/10.1038/s41467-021-24467-0
_version_ 1783722605665058816
author Bui, Linh T.
Winters, Nichelle I.
Chung, Mei-I
Joseph, Chitra
Gutierrez, Austin J.
Habermann, Arun C.
Adams, Taylor S.
Schupp, Jonas C.
Poli, Sergio
Peter, Lance M.
Taylor, Chase J.
Blackburn, Jessica B.
Richmond, Bradley W.
Nicholson, Andrew G.
Rassl, Doris
Wallace, William A.
Rosas, Ivan O.
Jenkins, R. Gisli
Kaminski, Naftali
Kropski, Jonathan A.
Banovich, Nicholas E.
author_facet Bui, Linh T.
Winters, Nichelle I.
Chung, Mei-I
Joseph, Chitra
Gutierrez, Austin J.
Habermann, Arun C.
Adams, Taylor S.
Schupp, Jonas C.
Poli, Sergio
Peter, Lance M.
Taylor, Chase J.
Blackburn, Jessica B.
Richmond, Bradley W.
Nicholson, Andrew G.
Rassl, Doris
Wallace, William A.
Rosas, Ivan O.
Jenkins, R. Gisli
Kaminski, Naftali
Kropski, Jonathan A.
Banovich, Nicholas E.
author_sort Bui, Linh T.
collection PubMed
description Patients with chronic lung disease (CLD) have an increased risk for severe coronavirus disease-19 (COVID-19) and poor outcomes. Here, we analyze the transcriptomes of 611,398 single cells isolated from healthy and CLD lungs to identify molecular characteristics of lung cells that may account for worse COVID-19 outcomes in patients with chronic lung diseases. We observe a similar cellular distribution and relative expression of SARS-CoV-2 entry factors in control and CLD lungs. CLD AT2 cells express higher levels of genes linked directly to the efficiency of viral replication and the innate immune response. Additionally, we identify basal differences in inflammatory gene expression programs that highlight how CLD alters the inflammatory microenvironment encountered upon viral exposure to the peripheral lung. Our study indicates that CLD is accompanied by changes in cell-type-specific gene expression programs that prime the lung epithelium for and influence the innate and adaptive immune responses to SARS-CoV-2 infection.
format Online
Article
Text
id pubmed-8280215
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-82802152021-07-23 Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity Bui, Linh T. Winters, Nichelle I. Chung, Mei-I Joseph, Chitra Gutierrez, Austin J. Habermann, Arun C. Adams, Taylor S. Schupp, Jonas C. Poli, Sergio Peter, Lance M. Taylor, Chase J. Blackburn, Jessica B. Richmond, Bradley W. Nicholson, Andrew G. Rassl, Doris Wallace, William A. Rosas, Ivan O. Jenkins, R. Gisli Kaminski, Naftali Kropski, Jonathan A. Banovich, Nicholas E. Nat Commun Article Patients with chronic lung disease (CLD) have an increased risk for severe coronavirus disease-19 (COVID-19) and poor outcomes. Here, we analyze the transcriptomes of 611,398 single cells isolated from healthy and CLD lungs to identify molecular characteristics of lung cells that may account for worse COVID-19 outcomes in patients with chronic lung diseases. We observe a similar cellular distribution and relative expression of SARS-CoV-2 entry factors in control and CLD lungs. CLD AT2 cells express higher levels of genes linked directly to the efficiency of viral replication and the innate immune response. Additionally, we identify basal differences in inflammatory gene expression programs that highlight how CLD alters the inflammatory microenvironment encountered upon viral exposure to the peripheral lung. Our study indicates that CLD is accompanied by changes in cell-type-specific gene expression programs that prime the lung epithelium for and influence the innate and adaptive immune responses to SARS-CoV-2 infection. Nature Publishing Group UK 2021-07-14 /pmc/articles/PMC8280215/ /pubmed/34262047 http://dx.doi.org/10.1038/s41467-021-24467-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bui, Linh T.
Winters, Nichelle I.
Chung, Mei-I
Joseph, Chitra
Gutierrez, Austin J.
Habermann, Arun C.
Adams, Taylor S.
Schupp, Jonas C.
Poli, Sergio
Peter, Lance M.
Taylor, Chase J.
Blackburn, Jessica B.
Richmond, Bradley W.
Nicholson, Andrew G.
Rassl, Doris
Wallace, William A.
Rosas, Ivan O.
Jenkins, R. Gisli
Kaminski, Naftali
Kropski, Jonathan A.
Banovich, Nicholas E.
Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity
title Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity
title_full Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity
title_fullStr Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity
title_full_unstemmed Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity
title_short Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity
title_sort chronic lung diseases are associated with gene expression programs favoring sars-cov-2 entry and severity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280215/
https://www.ncbi.nlm.nih.gov/pubmed/34262047
http://dx.doi.org/10.1038/s41467-021-24467-0
work_keys_str_mv AT builinht chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT wintersnichellei chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT chungmeii chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT josephchitra chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT gutierrezaustinj chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT habermannarunc chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT adamstaylors chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT schuppjonasc chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT polisergio chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT peterlancem chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT taylorchasej chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT blackburnjessicab chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT richmondbradleyw chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT nicholsonandrewg chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT rassldoris chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT wallacewilliama chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT rosasivano chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT jenkinsrgisli chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT kaminskinaftali chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT kropskijonathana chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT banovichnicholase chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity
AT chroniclungdiseasesareassociatedwithgeneexpressionprogramsfavoringsarscov2entryandseverity