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Anaerobic endosymbiont generates energy for ciliate host by denitrification

Author

Listed:
  • Jon S. Graf

    (Max Planck Institute for Marine Microbiology)

  • Sina Schorn

    (Max Planck Institute for Marine Microbiology)

  • Katharina Kitzinger

    (Max Planck Institute for Marine Microbiology
    University of Vienna)

  • Soeren Ahmerkamp

    (Max Planck Institute for Marine Microbiology)

  • Christian Woehle

    (Max Planck Institute for Plant Breeding Research)

  • Bruno Huettel

    (Max Planck Institute for Plant Breeding Research)

  • Carsten J. Schubert

    (Eawag)

  • Marcel M. M. Kuypers

    (Max Planck Institute for Marine Microbiology)

  • Jana Milucka

    (Max Planck Institute for Marine Microbiology)

Abstract

Mitochondria are specialized eukaryotic organelles that have a dedicated function in oxygen respiration and energy production. They evolved about 2 billion years ago from a free-living bacterial ancestor (probably an alphaproteobacterium), in a process known as endosymbiosis1,2. Many unicellular eukaryotes have since adapted to life in anoxic habitats and their mitochondria have undergone further reductive evolution3. As a result, obligate anaerobic eukaryotes with mitochondrial remnants derive their energy mostly from fermentation4. Here we describe ‘Candidatus Azoamicus ciliaticola’, which is an obligate endosymbiont of an anaerobic ciliate and has a dedicated role in respiration and providing energy for its eukaryotic host. ‘Candidatus A. ciliaticola’ contains a highly reduced 0.29-Mb genome that encodes core genes for central information processing, the electron transport chain, a truncated tricarboxylic acid cycle, ATP generation and iron–sulfur cluster biosynthesis. The genome encodes a respiratory denitrification pathway instead of aerobic terminal oxidases, which enables its host to breathe nitrate instead of oxygen. ‘Candidatus A. ciliaticola’ and its ciliate host represent an example of a symbiosis that is based on the transfer of energy in the form of ATP, rather than nutrition. This discovery raises the possibility that eukaryotes with mitochondrial remnants may secondarily acquire energy-providing endosymbionts to complement or replace functions of their mitochondria.

Suggested Citation

  • Jon S. Graf & Sina Schorn & Katharina Kitzinger & Soeren Ahmerkamp & Christian Woehle & Bruno Huettel & Carsten J. Schubert & Marcel M. M. Kuypers & Jana Milucka, 2021. "Anaerobic endosymbiont generates energy for ciliate host by denitrification," Nature, Nature, vol. 591(7850), pages 445-450, March.
  • Handle: RePEc:nat:nature:v:591:y:2021:i:7850:d:10.1038_s41586-021-03297-6
    DOI: 10.1038/s41586-021-03297-6
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    Cited by:

    1. Daan R. Speth & Linus M. Zeller & Jon S. Graf & Will A. Overholt & Kirsten Küsel & Jana Milucka, 2024. "Genetic potential for aerobic respiration and denitrification in globally distributed respiratory endosymbionts," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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