# Diel transcriptional dynamics of a marine sponge and its microbiome in a natural environment

**Authors:** Gustavo A. Ramírez, Rinat Bar-Shalom, Tzipora Perez, Reut Efrati Epchtien, Andrea Furlan, Roberto Romeo, Michelle Gavagnin, Arkadiy I. Garber, Maya Lalzar, Laura Steindler

PMC · DOI: 10.1186/s42523-025-00510-z · Animal Microbiome · 2026-02-05

## TL;DR

This study explores how marine sponges and their microbes change gene activity over a day-night cycle in their natural habitat.

## Contribution

The study reveals targeted diel transcriptional responses in sponge and specific microbial lineages, linking nitrogen assimilation, sulfur metabolism, and detoxification.

## Key findings

- Microbiome activity clusters by sponge host rather than time, but some microbial genes show diel patterns.
- Cyanobacterial symbionts use host-derived carbohydrates at night for nitrogen assimilation and energy.
- Sponge and alphaproteobacterial symbionts show synchronized diel regulation of detoxification and sulfur metabolism genes.

## Abstract

Marine sponges are ecologically critical animals that host diverse microbial communities, forming complex symbiotic systems crucial to nutrient cycling and ecosystem functioning in the ocean. While several studies have started to delineate the interactions between sponges and their microbiomes, whether and how these interactions are influenced by night and day cycles remains unclear, particularly in natural environments.

Here, we analyzed the in situ transcriptional changes of the demosponge species Aplysina aerophoba and its microbiome over a diel cycle, sampling four specimens each at four time points within a 24-hour period. At the global metatranscriptome level, microbiome activity clustered by animal subject, rather than time of sampling. However, diel transcriptional patterns were observed for a limited number of microbial genes, primarily involved in secondary metabolite biosynthesis and antibiotic efflux pumps. At the individual microbial lineage level, we identified diel patterns in cyanobacterial and alphaproteobacterial symbionts. Cyanobacterial symbionts exhibited canonical circadian regulation, with daytime expression of photosynthesis-related genes. At night upregulation of ammonium assimilation via glutamine synthetase coincided with induction of the oxidative pentose phosphate pathway and respiratory genes, indicating reliance on host-derived carbohydrates to generate ATP, NADPH, and the 2-oxoglutarate carbon backbone required for glutamate synthesis in the dark. This pattern contrasts with free-living cyanobacteria, where nitrogen assimilation is typically day-active and fueled by photosynthesis-derived energy and reducing power. The sponge host transcriptome displayed distinct diel regulation of key circadian genes (cry2 and PAR-bZIP), in addition to daytime upregulation of genes involved in sulfur metabolism and oxidative stress defense, patterns mirrored by alphaproteobacterial symbionts that together contribute to glutathione-based detoxification (sponge Glo2, bacterial GstB) and H2S management (SQOR).

Our study demonstrates that diel environmental fluctuations modulate the transcriptome of the sponge hosts and only select microbial lineages - primarily Cyanobacteria and heterotrophic Alphaproteobacteria – highlighting targeted rather than community-wide diel transcriptional responses within the holobiont. Together, these lineage-specific responses reveal mechanistic links between nitrogen assimilation, sulfur metabolism, and oxidative stress detoxification. These findings provide novel insights into the metabolic integration and functional stability of one of the earliest evolved animal-microbe symbiotic systems.

The online version contains supplementary material available at 10.1186/s42523-025-00510-z.

## Linked entities

- **Genes:** CRY2 (cryptochrome circadian regulator 2) [NCBI Gene 1408], HAGH (hydroxyacylglutathione hydrolase) [NCBI Gene 3029], GSTM3 (glutathione S-transferase mu 3) [NCBI Gene 2947], GSR2 (uncharacterized protein) [NCBI Gene 842935], SQOR (sulfide quinone oxidoreductase) [NCBI Gene 58472]
- **Species:** Aplysina aerophoba (taxon 289389), Alphaproteobacteria (taxon 28211)

## Full-text entities

- **Genes:** GSTM3 (glutathione S-transferase mu 3) [NCBI Gene 2947] {aka GST5, GSTB, GSTM3-3, GSTM3TV2, GTM3, hGSTM3-3}, ME1 (malic enzyme 1) [NCBI Gene 4199] {aka HUMNDME, MES}, BHMT (betaine--homocysteine S-methyltransferase) [NCBI Gene 635] {aka BHMT1, HEL-S-61p}, PGP (phosphoglycolate phosphatase) [NCBI Gene 283871] {aka AUM, G3PP, PGPase}, ASS1 (argininosuccinate synthase 1) [NCBI Gene 445] {aka ASS, CTLN1}, GABARAP (GABA type A receptor-associated protein) [NCBI Gene 11337] {aka ATG8A, GABARAP-a, MM46}, GLUL (glutamate-ammonia ligase) [NCBI Gene 2752] {aka DEE116, GLNS, GS, PIG43, PIG59}, CCT4 (chaperonin containing TCP1 subunit 4) [NCBI Gene 10575] {aka CCT-DELTA, Cctd, SRB}, AHCY (adenosylhomocysteinase) [NCBI Gene 191] {aka SAHH, adoHcyase}, GSTK1 (glutathione S-transferase kappa 1) [NCBI Gene 373156] {aka GST, GST 13-13, GST13, GST13-13, GSTK1-1, hGSTK1}, HAGH (hydroxyacylglutathione hydrolase) [NCBI Gene 3029] {aka GLO2, GLO2D, GLX2, GLXII, HAGH1}, FBXO3 (F-box protein 3) [NCBI Gene 26273] {aka FBA, FBX3}, TALDO1 (transaldolase 1) [NCBI Gene 6888] {aka TAL, TAL-H, TALDOR, TALH}, PDXK (pyridoxal kinase) [NCBI Gene 8566] {aka C21orf124, C21orf97, HEL-S-1a, HMSN6C, PKH, PNK}, CRY2 (cryptochrome circadian regulator 2) [NCBI Gene 1408] {aka HCRY2, PHLL2}, TALDO1P1 (transaldolase 1 pseudogene 1) [NCBI Gene 6889] {aka TAL-H, TALDO, TALDOP1}, FH (fumarate hydratase) [NCBI Gene 2271] {aka FMRD, HLRCC, HsFH, LRCC, MCL, MCUL1}, RAD51 (RAD51 recombinase) [NCBI Gene 5888] {aka BRCC5, FANCR, HRAD51, HsRad51, HsT16930, MRMV2}, DNAJB6 (DnaJ heat shock protein family (Hsp40) member B6) [NCBI Gene 10049] {aka DJ4, DnaJ, HHDJ1, HSJ-2, HSJ2, LGMD1D}, RN7SL263P (RNA, 7SL, cytoplasmic 263, pseudogene) [NCBI Gene 106480993], PAEP (progestagen associated endometrial protein) [NCBI Gene 5047] {aka GD, GdA, GdF, GdS, PAEG, PEP}, CHDH (choline dehydrogenase) [NCBI Gene 55349], MAG (myelin associated glycoprotein) [NCBI Gene 4099] {aka GMA, S-MAG, SIGLEC-4A, SIGLEC4, SIGLEC4A, SPG75}, CPE (carboxypeptidase E) [NCBI Gene 1363] {aka BDVS, CPH, IDDHH}, SQOR (sulfide quinone oxidoreductase) [NCBI Gene 58472] {aka CGI-44, PRO1975, SQR, SQRDL}
- **Diseases:** LS (MESH:D007888), pHMMs (MESH:D004195), TPM (OMIM:602482), MRN (MESH:D020423)
- **Chemicals:** nitrite (MESH:D009573), ATP (MESH:D000255), ice (MESH:D007053), B12 (MESH:C034730), ROS (MESH:D017382), arginine (MESH:D001120), Homocysteine (MESH:D006710), oxygen (MESH:D010100), carbohydrate (MESH:D002241), taurine (MESH:D013654), pentose phosphate (MESH:D010428), sulfide (MESH:D013440), C (MESH:D002244), glycogen (MESH:D006003), NADPH (MESH:D009249), aromatic hydrocarbon (MESH:D006841), sulfite (MESH:D013447), SYBR green (MESH:C098022), beta-carotene (MESH:D019207), NADH (MESH:D009243), amino acids (MESH:D000596), S-adenosylhomocysteine (MESH:D012435), betaine (MESH:D001622), Ammonium (MESH:D064751), glucose (MESH:D005947), inositol (MESH:D007294), choline (MESH:D002794), sulfonate (MESH:D000476), N (MESH:D009584), glutamate (MESH:D018698), cobalamin (MESH:D014805), S-adenosylmethionine (MESH:D012436), glutathione (MESH:D005978), TCA (MESH:D014238), ammonia (MESH:D000641), 2-oxoglutarate (MESH:D007656), carnitine (MESH:D002331), sulfate (MESH:D013431), Sulfur (MESH:D013455), vitamin B6 (MESH:D025101), carotenoid (MESH:D002338), cysteine (MESH:D003545), H2S (MESH:D006862), 2-oxoglutarate carbon (-), Methionine (MESH:D008715), NO (MESH:D009569)
- **Species:** Candidatus Poribacteria (phylum) [taxon 265317], Mus musculus (house mouse, species) [taxon 10090], Chloroflexota (GNS bacteria, phylum) [taxon 200795], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Aplysina aerophoba (species) [taxon 289389], Acidobacteriota (phylum) [taxon 57723], Candidatus Synechococcus spongiarum (species) [taxon 431041], Amphimedon queenslandica (species) [taxon 400682], Dehalococcoidia (class) [taxon 301297], Cyanobacteriota (blue-green algae, phylum) [taxon 1117], Porifera (sponges, phylum) [taxon 6040]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12879404/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12879404/full.md

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Source: https://tomesphere.com/paper/PMC12879404