A polarized cell system amenable to subcellular resolution imaging of influenza virus infection

PLoS One. 2024 Jan 25;19(1):e0292977. doi: 10.1371/journal.pone.0292977. eCollection 2024.

Abstract

The life cycle of influenza A viruses (IAV), and notably intracellular trafficking of the viral genome, depends on multiple interactions with the cellular cytoskeleton and endomembrane system. A limitation of the conventional cellular models used for mechanistic study and subcellular imaging of IAV infection is that they are cultured in two dimensions (2D) under non-polarizing conditions, and therefore they do not recapitulate the intracellular organization of the polarized respiratory epithelial cells naturally targeted by IAVs. To overcome this limitation, we developed an IAV-infection assay in a 3D cell culture system which allows imaging along the baso-lateral axis of polarized cells, with subcellular resolution. Here we describe a protocol to grow polarized monolayers of Caco2-TC7 cells on static Cytodex-3 microcarrier beads, infect them with IAV, and subsequently perform immunostaining and confocal imaging, or electron microscopy, on polarized IAV-infected cells. This method can be extended to other pathogens that infect human polarized epithelial cells.

MeSH terms

  • Caco-2 Cells
  • Epithelial Cells / metabolism
  • Humans
  • Influenza A virus*
  • Influenza, Human*
  • Orthomyxoviridae Infections*
  • Virus Replication

Grants and funding

NN: HFSP-RGP0040/2019 https://www.hfsp.org/ NN and AM: ANR-10-LABX-62-IBEID https://anr.fr/ NN and LD: ANR-21-CE11-0010-03 https://anr.fr/ AM: ANR-10-INSB-04-01 and ANR-10–INBS-04 LD: ANR-10-INBS-04 https://anr.fr/ The funders did not and will not have a role in study design, data collection and analysis, decision to publish, or preparation of the manuscript."