An organoid-derived bronchioalveolar model for SARS-CoV-2 infection of human alveolar type II-like cells

  • Mart M. Lamers
  • , Jelte van der Vaart
  • , Kèvin 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

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

185 Citaten (Scopus)

Samenvatting

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.

Originele taal-2Engels
Artikelnummere105912
TijdschriftEMBO Journal
Volume40
Nummer van het tijdschrift5
DOI's
StatusGepubliceerd - 1 mrt. 2021
Extern gepubliceerdJa

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