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An organoid‐derived bronchioalveolar model for SARS‐CoV‐2 infection of human alveolar type II‐like cells
Authors:Mart M Lamers,Jelte van der Vaart,K  vin Knoops,Samra Riesebosch,Tim I Breugem,Anna Z Mykytyn,Joep Beumer,Debby Schipper,Karel Bezstarosti,Charlotte D Koopman,Nathalie Groen,Raimond B G Ravelli,Hans Q Duimel,Jeroen A A Demmers,Georges M G M Verjans,Marion P G Koopmans,Mauro J Muraro,Peter J Peters,Hans Clevers,Bart L Haagmans
Affiliation:1. Viroscience Department, Erasmus University Medical Center, Rotterdam The Netherlands ; 2. Oncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center, Utrecht The Netherlands ; 3. The Maastricht Multimodal Molecular Imaging Institute, Maastricht University, Maastricht The Netherlands ; 4. Proteomics Center, Erasmus University Medical Center, Rotterdam The Netherlands ; 5. Single Cell Discoveries, Utrecht The Netherlands
Abstract: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.
Keywords:airway organoids, bronchioalveolar‐  like, COVID‐  19, pneumocytes, SARS‐  CoV‐  2
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