Chronic lung diseases are associated with gene expression programs favoring SARS-CoV-2 entry and severity
Autor: | Nichelle I. Winters, Taylor Adams, Jessica B. Blackburn, Mei-I Chung, Andrew G. Nicholson, William A Wallace, Bradley W. Richmond, Naftali Kaminski, Jonas C. Schupp, Sergio Poli, Linh T. Bui, Austin J. Gutierrez, Lance M. Peter, Chase J. Taylor, Chitra Joseph, Ivan O. Rosas, Jonathan A. Kropski, R. Gisli Jenkins, Arun C. Habermann, Doris Rassl, Nicholas E. Banovich |
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Přispěvatelé: | Groningen Research Institute for Asthma and COPD (GRIAC), Bui, Linh T [0000-0003-3152-8978], Joseph, Chitra [0000-0003-2631-9266], Gutierrez, Austin J [0000-0003-2977-2189], Schupp, Jonas C [0000-0002-7714-8076], Poli, Sergio [0000-0001-5442-3189], Richmond, Bradley W [0000-0001-6200-5235], Wallace, William A [0000-0002-4752-7956], Jenkins, R Gisli [0000-0002-7929-2119], Kaminski, Naftali [0000-0001-5917-4601], Apollo - University of Cambridge Repository |
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Lung Diseases General Physics and Astronomy medicine.disease_cause Virus Replication Transcriptome 0302 clinical medicine Pulmonary fibrosis Gene expression Lung Coronavirus COPD Multidisciplinary respiratory system medicine.anatomical_structure 030220 oncology & carcinogenesis RECEPTOR ACE2 Angiotensin-Converting Enzyme 2 congenital hereditary and neonatal diseases and abnormalities Immunopathogenesis Science Article General Biochemistry Genetics and Molecular Biology 03 medical and health sciences Immune system Immunity medicine Humans Inflammation Innate immune system business.industry SARS-CoV-2 COVID-19 General Chemistry Virus Internalization medicine.disease Idiopathic Pulmonary Fibrosis Immunity Innate Computational biology and bioinformatics respiratory tract diseases 030104 developmental biology Viral replication Viral infection Alveolar Epithelial Cells Immunology Chronic Disease business |
Zdroj: | Nature Communications, 12(1):4314. Nature Publishing Group Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021) Nature Communications |
ISSN: | 2041-1723 |
Popis: | 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. Patients with chronic lung disease (CLD) have an increased risk for severe coronavirus disease-19 and poor outcomes. Here the authors compare the transcriptomes of single cells isolated from healthy and CLD lungs to identify molecular characteristics of lung cells that may account for worse COVID-19 outcomes in these patients. |
Databáze: | OpenAIRE |
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