An organoid-derived bronchioalveolar model for SARS-CoV-2 infection of human alveolar type II-like cells.
Mart M LamersJelte van der VaartKèvin KnoopsSamra RieseboschTim I BreugemAnna Z MykytynJoep BeumerDebby SchipperKarel BezstarostiCharlotte D KoopmanNathalie GroenRaimond B G RavelliHans Q DuimelJeroen A A DemmersGeorges G M G M VerjansMarion P G KoopmansMauro J MuraroPeter J PetersHans CleversBart L HaagmansPublished in: The EMBO journal (2021)
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.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- acute respiratory distress syndrome
- induced apoptosis
- low dose
- single cell
- cell cycle arrest
- endothelial cells
- extracorporeal membrane oxygenation
- induced pluripotent stem cells
- mechanical ventilation
- binding protein
- high throughput
- endoplasmic reticulum stress
- optical coherence tomography
- emergency department
- electron microscopy
- drug delivery
- oxidative stress
- intensive care unit
- rna seq
- dna methylation
- genome wide
- amino acid
- ionic liquid
- genome wide identification