Abstract
Chemosynthetic symbioses are partnerships between invertebrate animals and chemosynthetic bacteria. The latter are the primary producers, providing most of the organic carbon needed for the animal host's nutrition. We sequenced genomes of the chemosynthetic symbionts from the lucinid bivalve Loripes lucinalis and the stilbonematid nematode Laxus oneistus. The symbionts of both host species encoded nitrogen fixation genes. This is remarkable as no marine chemosynthetic symbiont was previously known to be capable of nitrogen fixation. We detected nitrogenase expression by the symbionts of lucinid clams at the transcriptomic and proteomic level. Mean stable nitrogen isotope values of Loripes lucinalis were within the range expected for fixed atmospheric nitrogen, further suggesting active nitrogen fixation by the symbionts. The ability to fix nitrogen may be widespread among chemosynthetic symbioses in oligotrophic habitats, where nitrogen availability often limits primary productivity.
Highlights
Chemosynthetic symbioses are partnerships between invertebrate animals and chemosynthetic bacteria
Most studies have focused on inorganic carbon fixation by the symbionts and the transfer of fixed organic carbon compounds to the hosts
We focused on the symbiosis between Loripes lucinalis (Lamarck, 1818) and its endosymbionts
Summary
Chemosynthetic symbioses are partnerships between invertebrate animals and chemosynthetic bacteria. As expected based on previous studies of symbiont metabolism, genes and pathways for sulfur oxidation and carbon fixation were found in all five Ca. Thiodiazotropha endoloripes and in both Ca. Thiosymbion oneisti draft symbiont genomes (Fig. 2).
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