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  Hydrogenotrophic methanogenesis is the key process in the obligately syntrophic consortium of the anaerobic ameba Pelomyxa schiedti

Treitli, S. C., Hanousková, P., Beneš, V., Brune, A., Čepička, I., & Hampl, V. (2023). Hydrogenotrophic methanogenesis is the key process in the obligately syntrophic consortium of the anaerobic ameba Pelomyxa schiedti. The ISME Journal, 17(11), 1884-1894. doi:10.1038/s41396-023-01499-6.

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https://doi.org/10.1038/s41396-023-01499-6 (Publisher version)
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 Creators:
Treitli, Sebastian C.1, Author
Hanousková, Pavla1, Author
Beneš, Vladimír1, Author
Brune, Andreas2, Author                 
Čepička, Ivan1, Author
Hampl, Vladimír1, Author
Affiliations:
1external, ou_persistent22              
2Department-Independent Research Group Insect Gut Microbiology and Symbiosis, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266271              

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 Abstract: Pelomyxa is a genus of anaerobic amoebae that live in consortia with multiple prokaryotic endosymbionts. Although the symbionts represent a large fraction of the cellular biomass, their metabolic roles have not been investigated. Using single-cell genomics and transcriptomics, we have characterized the prokaryotic community associated with P. schiedti, which is composed of two bacteria, Candidatus Syntrophus pelomyxae (class Deltaproteobacteria) and Candidatus Vesiculincola pelomyxae (class Clostridia), and a methanogen, Candidatus Methanoregula pelomyxae. Fluorescence in situ hybridization and electron microscopy showed that Ca. Vesiculincola pelomyxae is localized inside vesicles, whereas the other endosymbionts occur freely in the cytosol, with Ca. Methanoregula pelomyxae enriched around the nucleus. Genome and transcriptome-based reconstructions of the metabolism suggests that the cellulolytic activity of P. schiedti produces simple sugars that fuel its own metabolism and the metabolism of a Ca. Vesiculincola pelomyxae, while Ca. Syntrophus pelomyxae energy metabolism relies on degradation of butyrate and isovalerate from the environment. Both species of bacteria and the ameba use hydrogenases to transfer the electrons from reduced equivalents to hydrogen, a process that requires a low hydrogen partial pressure. This is achieved by the third endosymbiont, Ca. Methanoregula pelomyxae, which consumes H2 and formate for methanogenesis. While the bacterial symbionts can be successfully eliminated by vancomycin treatment without affecting the viability of the amoebae, treatment with 2-bromoethanesulfonate, a specific inhibitor of methanogenesis, killed the amoebae, indicating the essentiality of the methanogenesis for this consortium.

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Language(s): eng - English
 Dates: 2023
 Publication Status: Issued
 Pages: -
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 Rev. Type: Peer
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Title: The ISME Journal
  Other : The ISME journal : multidisciplinary journal of microbial ecology
  Abbreviation : ISME J.
Source Genre: Journal
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Publ. Info: Basingstoke : Nature Publishing Group
Pages: - Volume / Issue: 17 (11) Sequence Number: - Start / End Page: 1884 - 1894 Identifier: ISSN: 1751-7370
ISSN: 1751-7362
CoNE: https://pure.mpg.de/cone/journals/resource/1751-7370