Host cell-specific metabolism of linoleic acid controls Toxoplasma gondii growth in cell culture.
Nicole D HryckowianCaitlin ZindaSung Chul ParkMartin T KeltyLaura J KnollPublished in: bioRxiv : the preprint server for biology (2024)
The obligate intracellular parasite Toxoplasma gondii can infect and replicate in any warm-blooded cell tested to date, but much of our knowledge about T. gondii cell biology comes from just one host cell type: human foreskin fibroblasts (HFFs). To expand our knowledge of host-parasite lipid interactions, we studied T. gondii in intestinal epithelial cells, the first site of host-parasite contact following oral infection and the exclusive site of parasite sexual development in feline hosts. We found that highly metabolic Caco-2 cells are permissive to T. gondii growth even when treated with high levels of linoleic acid (LA), a polyunsaturated fatty acid (PUFA) that kills parasites in HFFs. Caco-2 cells appear to sequester LA away from the parasite, preventing membrane disruptions and lipotoxicity that characterize LA-induced parasite death in HFFs. Our work is an important step toward understanding host-parasite interactions in feline intestinal epithelial cells, an understudied but important cell type in the T. gondii life cycle.
Keyphrases
- toxoplasma gondii
- life cycle
- fatty acid
- plasmodium falciparum
- single cell
- induced apoptosis
- cell therapy
- healthcare
- cell cycle arrest
- endothelial cells
- trypanosoma cruzi
- mental health
- stem cells
- cell death
- mesenchymal stem cells
- signaling pathway
- cell proliferation
- induced pluripotent stem cells
- pluripotent stem cells