TY - JOUR
T1 - An organoid-derived bronchioalveolar model for SARS-CoV-2 infection of human alveolar type II-like cells
AU - Lamers, Mart
AU - Vaart, J
AU - Knoops, K
AU - Riesebosch, S (Samra)
AU - Breugem, Tim
AU - Mykytyn, Anna
AU - Beumer, J
AU - van Eck - Schipper, Debby
AU - Bezstarosti, Karel
AU - Koopman, CD
AU - Groen, N
AU - Ravelli, RBG
AU - Duimel, HQ
AU - Demmers, Jeroen
AU - Verjans, Georges
AU - Koopmans, Marion
AU - Muraro, MJ
AU - Peters, PJ
AU - Clevers, H
AU - Haagmans, Bart
PY - 2021/3/1
Y1 - 2021/3/1
N2 - Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), which may result in acute respiratory distress syndrome (ARDS), multiorgan failure, and death. The alveolar epithelium is a major target of the virus, but representative models to study virus host interactions in more detail are currently lacking. Here, we describe a human 2D air–liquid interface culture system which was characterized by confocal and electron microscopy and single-cell mRNA expression analysis. In this model, alveolar cells, but also basal cells and rare neuroendocrine cells, are grown from 3D self-renewing fetal lung bud tip organoids. These cultures were readily infected by SARS-CoV-2 with mainly surfactant protein C-positive alveolar type II-like cells being targeted. Consequently, significant viral titers were detected and mRNA expression analysis revealed induction of type I/III interferon response program. Treatment of these cultures with a low dose of interferon lambda 1 reduced viral replication. Hence, these cultures represent an experimental model for SARS-CoV-2 infection and can be applied for drug screens.
AB - Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), which may result in acute respiratory distress syndrome (ARDS), multiorgan failure, and death. The alveolar epithelium is a major target of the virus, but representative models to study virus host interactions in more detail are currently lacking. Here, we describe a human 2D air–liquid interface culture system which was characterized by confocal and electron microscopy and single-cell mRNA expression analysis. In this model, alveolar cells, but also basal cells and rare neuroendocrine cells, are grown from 3D self-renewing fetal lung bud tip organoids. These cultures were readily infected by SARS-CoV-2 with mainly surfactant protein C-positive alveolar type II-like cells being targeted. Consequently, significant viral titers were detected and mRNA expression analysis revealed induction of type I/III interferon response program. Treatment of these cultures with a low dose of interferon lambda 1 reduced viral replication. Hence, these cultures represent an experimental model for SARS-CoV-2 infection and can be applied for drug screens.
UR - http://www.scopus.com/inward/record.url?scp=85099097921&partnerID=8YFLogxK
U2 - 10.15252/embj.2020105912
DO - 10.15252/embj.2020105912
M3 - Article
C2 - 33283287
SN - 0261-4189
VL - 40
JO - EMBO Journal
JF - EMBO Journal
IS - 5
M1 - e105912
ER -