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SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery
Coronavirus disease 2019 (COVID-19) is the latest respiratory pandemic resulting from zoonotic transmission of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2). Severe symptoms include viral pneumonia secondary to infection and inflammation of the lower respiratory tract, in some...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337376/ https://www.ncbi.nlm.nih.gov/pubmed/32637946 http://dx.doi.org/10.1101/2020.06.29.174623 |
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author | Mulay, A. Konda, B. Garcia, G. Yao, C. Beil, S. Sen, C. Purkayastha, A. Kolls, J. K. Pociask, D. A. Pessina, P. de Aja, J. Sainz Garcia-de-Alba, C. Kim, C. F. Gomperts, B. Arumugaswami, V. Stripp, B.R. |
author_facet | Mulay, A. Konda, B. Garcia, G. Yao, C. Beil, S. Sen, C. Purkayastha, A. Kolls, J. K. Pociask, D. A. Pessina, P. de Aja, J. Sainz Garcia-de-Alba, C. Kim, C. F. Gomperts, B. Arumugaswami, V. Stripp, B.R. |
author_sort | Mulay, A. |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) is the latest respiratory pandemic resulting from zoonotic transmission of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2). Severe symptoms include viral pneumonia secondary to infection and inflammation of the lower respiratory tract, in some cases causing death. We developed primary human lung epithelial infection models to understand responses of proximal and distal lung epithelium to SARS-CoV-2 infection. Differentiated air-liquid interface cultures of proximal airway epithelium and 3D organoid cultures of alveolar epithelium were readily infected by SARS-CoV-2 leading to an epithelial cell-autonomous proinflammatory response. We validated the efficacy of selected candidate COVID-19 drugs confirming that Remdesivir strongly suppressed viral infection/replication. We provide a relevant platform for studying COVID-19 pathobiology and for rapid drug screening against SARS-CoV-2 and future emergent respiratory pathogens. |
format | Online Article Text |
id | pubmed-7337376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-73373762020-07-07 SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery Mulay, A. Konda, B. Garcia, G. Yao, C. Beil, S. Sen, C. Purkayastha, A. Kolls, J. K. Pociask, D. A. Pessina, P. de Aja, J. Sainz Garcia-de-Alba, C. Kim, C. F. Gomperts, B. Arumugaswami, V. Stripp, B.R. bioRxiv Article Coronavirus disease 2019 (COVID-19) is the latest respiratory pandemic resulting from zoonotic transmission of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2). Severe symptoms include viral pneumonia secondary to infection and inflammation of the lower respiratory tract, in some cases causing death. We developed primary human lung epithelial infection models to understand responses of proximal and distal lung epithelium to SARS-CoV-2 infection. Differentiated air-liquid interface cultures of proximal airway epithelium and 3D organoid cultures of alveolar epithelium were readily infected by SARS-CoV-2 leading to an epithelial cell-autonomous proinflammatory response. We validated the efficacy of selected candidate COVID-19 drugs confirming that Remdesivir strongly suppressed viral infection/replication. We provide a relevant platform for studying COVID-19 pathobiology and for rapid drug screening against SARS-CoV-2 and future emergent respiratory pathogens. Cold Spring Harbor Laboratory 2020-06-29 /pmc/articles/PMC7337376/ /pubmed/32637946 http://dx.doi.org/10.1101/2020.06.29.174623 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY-ND 4.0 International license (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Article Mulay, A. Konda, B. Garcia, G. Yao, C. Beil, S. Sen, C. Purkayastha, A. Kolls, J. K. Pociask, D. A. Pessina, P. de Aja, J. Sainz Garcia-de-Alba, C. Kim, C. F. Gomperts, B. Arumugaswami, V. Stripp, B.R. SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery |
title | SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery |
title_full | SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery |
title_fullStr | SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery |
title_full_unstemmed | SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery |
title_short | SARS-CoV-2 infection of primary human lung epithelium for COVID-19 modeling and drug discovery |
title_sort | sars-cov-2 infection of primary human lung epithelium for covid-19 modeling and drug discovery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337376/ https://www.ncbi.nlm.nih.gov/pubmed/32637946 http://dx.doi.org/10.1101/2020.06.29.174623 |
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