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Nature Communications· 2026Q1

A multilamellar organelle for chemosymbiosis in an aplacophoran mollusc adapted to anoxic cold seep sediment

Yunlong Li, Chong Chen, Xu Liu, Menggong Li et al.

Short summary

A novel organelle, termed 'dracosphera', has been identified within the aplacophoran mollusc Chaetoderma shenloong, housing symbiotic sulfur-oxidizing bacteria in multilamellar compartments (~12 μm) for chemosynthesis in anoxic sediments.

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Key points

  • A new organelle, 'dracosphera', has been identified in the aplacophoran mollusc Chaetoderma shenloong.
  • The dracosphera contains symbiotic sulfur-oxidizing bacteria within multilamellar compartments (~12 μm).
  • This organelle is located in the hypertrophied digestive gland of the mollusc, which has a reduced gut.
  • Genomic and transcriptomic analyses suggest the dracosphera minimizes oxygen diffusion to the anaerobic bacteria.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Symbiosis with chemoautotrophic bacteria has evolved in many animal lineages inhabiting reducing habitats such as hydrothermal vents, allowing these holobionts to thrive in dark biospheres 1 . In certain instances, the symbionts have become intracellular, residing within specialised bacteriocytes 2 . The integration of microbial symbionts with eukaryotic cells vary across known animals; however, no specialised organelle dedicated to chemosynthesis has been identified yet 2 . Here, we report a mode of symbiosis where sulphur-oxidising bacteria cultured within spherical multilamellar compartments (~12 μm) in the cold-seep aplacophoran mollusc Chaetoderma shenloong . This organelle, which we name ‘dracosphera’, is ubiquitous within the hypertrophied and intricately reticulate digestive gland of C. shenloong , which has otherwise lost most of its gut. Given that the symbionts are strictly anaerobic and the host resides in anoxic sediments tens of centimetres below the surface, the dracosphera may serve to minimise oxygen diffusion to the bacteria, akin to mechanisms observed in microbial diazotrophs 3 or termite hindguts 4 , as supported by our genomic and spatial transcriptomic analyses. Hypoxic conditions have been known to induce radical adaptations in meiofauna, exemplified by the acquisition of hydrogenosomes 5 . Our discovery of similarly exceptional adaptations in C. shenloong provides new insights into the evolution of such organelles also in larger animals.

The authors' abstract, as published at the source. Nature Communications, 2026 · DOI ↗

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OceanographyEarth and Planetary Sciences