Abstract

Symbiont relationships between corals and photosynthetic microorganisms sustain coral reef existence. However, the Great Amazon Reef System (GARS) stays under a plume layer that attenuates the entry of light, and instead of corals, sponges are the major reef epifauna, for which little is known about the function of the associated microbiome. Here, we used genome-resolved metagenomics to investigate how the sponge microbiome supports its host and overcomes the reduced light availability, recovering 205 MAGs from Agelas and Geodia sponges with completeness >70% and contamination <10%. Beta diversity estimates based on the 16S rRNA genes indicated the microbiomes of Amazon and Caribbean sponges to be distinct (P<0.01), with heterotrophic lifestyles being prevalent in Amazon sponge microbiomes (P<0.05). Nevertheless, genes indicating the carbon fixation pathways 3-Hydroxypropionate/4-Hydroxybutyrate cycle, 3-Hydroxypropionate bicycle, Reductive Tricarboxylic Acid Cycle, and Calvin-Benson-Bassham cycle could be recovered in low abundance. The presence of Cyanobacteria, represented by both 16S rRNA analyses and low-quality MAGs indicated light incidence on the reef. The metabolic profile shows that the GARS sponge microbiome had genes for sulfate reduction, sulfur oxidation, nitric oxide reduction, ammonia oxidation, nitrate reduction, nitrite ammonification, nitrite oxidation, and nitrite reduction, indicating that the microbiome might play a role in detoxification of the holobiont. We conclude, that neither the plume-limited photosynthesis of the sponge microbiome nor the primary producers sustain the organic carbon input for the sponges, which likely live off plume-associated organic carbon and their heterotrophic microbiota.

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