Trans-cellular tunnels induced by the fungal pathogen Candida albicans facilitate invasion through successive epithelial cells without host damage.
Joy LachatAlice PascaultDelphine ThibautRémi Le BorgneJean-Marc VerbavatzAllon WeinerPublished in: Nature communications (2022)
The opportunistic fungal pathogen Candida albicans is normally commensal, residing in the mucosa of most healthy individuals. In susceptible hosts, its filamentous hyphal form can invade epithelial layers leading to superficial or severe systemic infection. Although invasion is mainly intracellular, it causes no apparent damage to host cells at early stages of infection. Here, we investigate C. albicans invasion in vitro using live-cell imaging and the damage-sensitive reporter galectin-3. Quantitative single cell analysis shows that invasion can result in host membrane breaching at different stages and host cell death, or in traversal of host cells without membrane breaching. Membrane labelling and three-dimensional 'volume' electron microscopy reveal that hyphae can traverse several host cells within trans-cellular tunnels that are progressively remodelled and may undergo 'inflations' linked to host glycogen stores. Thus, C. albicans early invasion of epithelial tissues can lead to either host membrane breaching or trans-cellular tunnelling.
Keyphrases
- candida albicans
- biofilm formation
- induced apoptosis
- cell death
- cell cycle arrest
- cell migration
- single cell
- gene expression
- magnetic resonance imaging
- magnetic resonance
- computed tomography
- dna methylation
- genome wide
- rna seq
- signaling pathway
- mass spectrometry
- escherichia coli
- cystic fibrosis
- early onset
- reactive oxygen species