| Autor: |
Jerlström-Hultqvist, Jon, Gallot-Lavallée, Lucie, Salas-Leiva, Dayana E., Curtis, Bruce A., Záhonová, Kristína, Čepička, Ivan, Stairs, Courtney W., Pipaliya, Shweta, Dacks, Joel B., Archibald, John M., Roger, Andrew J. |
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| Zdroj: |
Nature Communications; 11/9/2024, Vol. 15 Issue 1, p1-15, 15p |
| Abstrakt: |
Symbiotic relationships between eukaryotes and prokaryotes played pivotal roles in the evolution of life and drove the emergence of specialized symbiotic structures in animals, plants and fungi. The host-evolved symbiotic structures of microbial eukaryotes – the vast majority of such hosts in nature – remain largely unstudied. Here we describe highly structured symbiosomes within three free-living anaerobic protists (Anaeramoeba spp.). We dissect this symbiosis using complete genome sequencing and transcriptomics of host and symbiont cells coupled with fluorescence in situ hybridization, and 3D reconstruction using focused-ion-beam scanning electron microscopy. The emergence of the symbiosome is underpinned by expansion of gene families encoding regulators of membrane trafficking and phagosomal maturation and extensive bacteria-to-eukaryote lateral transfer. The symbionts reside deep within a symbiosomal membrane network that enables metabolic syntrophy by precisely positioning sulfate-reducing bacteria alongside host hydrogenosomes. Importantly, the symbionts maintain connections to the Anaeramoeba plasma membrane, blurring traditional boundaries between ecto- and endosymbiosis. Symbiont-housing structures are well-studied in multicellular eukaryotes but rarely in unicellular protists. This study shows that low-oxygen-adapted Anaeramoebae have symbiosomes positioning sulfate-reducing bacteria near hydrogenosomes, with genomic analyses suggesting likely metabolic interactions. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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