4.8 Article

Archaeal extracellular vesicles are produced in an ESCRT-dependent manner and promote gene transfer and nutrient cycling in extreme environments

Journal

ISME JOURNAL
Volume 15, Issue 10, Pages 2892-2905

Publisher

SPRINGERNATURE
DOI: 10.1038/s41396-021-00984-0

Keywords

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Funding

  1. l'Agence Nationale de la Recherche [ANR-17-CE15-0005-01]
  2. Ville de Paris Emergence(s) program (project MEMREMA)
  3. European Research Council grant from the European Union's Seventh Framework Program (FP/2007-2013)/Project EVOMOBIL-ERC Grant [340440]
  4. PRESTIGE post-doctoral program from European Union's Seventh Framework Programme
  5. National Key Research and Development Program of China [2020YFA0906800]
  6. State Key Laboratory of Microbial Technology, Shandong University
  7. French National Research Agency (France BioImaging
  8. Investments for the Future) [ANR-10-INSB-04]
  9. Agence Nationale de la Recherche (ANR) [ANR-17-CE15-0005] Funding Source: Agence Nationale de la Recherche (ANR)

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Membrane-bound extracellular vesicles (EVs) are secreted by cells from all three domains of life, carrying a diverse proteome and DNA, and can support bacterial growth in extreme environments. The production of EVs in bacteria is mediated by the ESCRT machinery, with a prime role of ESCRT-III-1 and ESCRT-III-2 proteins in EV budding. EVs have deep evolutionary roots and play a crucial role in horizontal gene transfer and nutrient cycling in extreme environments.
Membrane-bound extracellular vesicles (EVs), secreted by cells from all three domains of life, transport various molecules and act as agents of intercellular communication in diverse environments. Here we demonstrate that EVs produced by a hyperthermophilic and acidophilic archaeon Sulfolobus islandicus carry not only a diverse proteome, enriched in membrane proteins, but also chromosomal and plasmid DNA, and can transfer this DNA to recipient cells. Furthermore, we show that EVs can support the heterotrophic growth of Sulfolobus in minimal medium, implicating EVs in carbon and nitrogen fluxes in extreme environments. Finally, our results indicate that, similar to eukaryotes, production of EVs in S. islandicus depends on the archaeal ESCRT machinery. We find that all components of the ESCRT apparatus are encapsidated into EVs. Using synchronized S. islandicus cultures, we show that EV production is linked to cell division and appears to be triggered by increased expression of ESCRT proteins during this cell cycle phase. Using a CRISPR-based knockdown system, we show that archaeal ESCRT-III and AAA+ ATPase Vps4 are required for EV production, whereas archaea-specific component CdvA appears to be dispensable. In particular, the active EV production appears to coincide with the expression patterns of ESCRT-III-1 and ESCRT-III-2, rather than ESCRT-III, suggesting a prime role of these proteins in EV budding. Collectively, our results suggest that ESCRT-mediated EV biogenesis has deep evolutionary roots, likely predating the divergence of eukaryotes and archaea, and that EVs play an important role in horizontal gene transfer and nutrient cycling in extreme environments.

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