# Cetobacterium alleviates the lipid accumulation in Nile tilapia (Oreochromis niloticus) induced by leucine addition

**Authors:** Miao Wang, Chenglin Tang, Zhigang Liu, Jianmeng Cao, Zhang Wang, Maixin Lu, Mengmeng Yi, Xiaoli Ke

PMC · DOI: 10.3389/fmicb.2025.1708010 · Frontiers in Microbiology · 2026-01-16

## TL;DR

Excess leucine in tilapia diets causes metabolic issues, but the gut bacterium Cetobacterium helps reduce these negative effects.

## Contribution

Identifies Cetobacterium as a beneficial gut microbe that mitigates leucine-induced lipid metabolism disorders in tilapia.

## Key findings

- High leucine diets caused growth inhibition and elevated lipid levels in tilapia.
- Cetobacterium intervention reduced serum cholesterol and hepatic lipid-droplet area in leucine-fed tilapia.
- Excess leucine activated mTOR signaling and upregulated lipogenic genes like IRS1 and ACC.

## Abstract

Deviation from the optimal dietary leucine range has been shown to have negative effects on fish growth and metabolism. This study investigated the dose-dependent effects of dietary leucine on lipid metabolism in Nile tilapia (Oreochromis niloticus). Four diets were formulated: a control diet containing the basal leucine level (2.3% of diet) and three test diets supplemented with 0.8, 1.6%, or 2.4% leucine, respectively. After 12 weeks of feeding, fish receiving ≥ 0.8% supplemental leucine showed significant growth inhibition (lower body weight and total length) and metabolic disorders, including hyperinsulinaemia and elevated serum total cholesterol (TC) and triglycerides (TG) levels, together with increased hepatic lipid-droplet area. Tilapia in the 2.4% leucine-addition group exhibited a markedly higher hepatosomatic index (HSI), whereas blood glucose was significantly reduced in tilapia of the 1.6 and 2.4% leucine-addition groups. Liver transcriptome comparison (2.4% leucine-addition vs. control) revealed activation of amino acid synthesis and the mTOR signaling pathway. qRT-PCR confirmed that excessive leucine up-regulated the expression of key lipogenic genes, such as IRS1 and ACC. 16S rRNA sequencing further revealed a 2.3-fold increase in the relative abundance of Cetobacterium in the intestine of the 2.4% leucine-addition group. Subsequent intervention with Cetobacterium somerae NK01 significantly reversed leucine-induced metabolic disorders, with a decrease in serum TC and TG levels by 7.8 and 10%, respectively, and a 58.3% reduction in hepatic lipid-droplet area. These beneficial effects were associated with the modulation of lipid-related genes, including IRS1, PI3K, SREBP1c, ACC, and FAS. Collectively, the data demonstrated a dual role of leucine in tilapia lipid metabolism: it promoted lipid lipogenesis by activating the mTOR-SREBP1c signaling axis while simultaneously enriching the intestinal symbiont Cetobacterium to alleviate metabolic stress.

## Linked entities

- **Genes:** IRS1 (insulin receptor substrate 1) [NCBI Gene 3667], ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 31], Srebf1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 78968], FAS (Fas cell surface death receptor) [NCBI Gene 355], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290]
- **Chemicals:** leucine (PubChem CID 857)
- **Species:** Oreochromis niloticus (taxon 8128), Cetobacterium somerae (taxon 188913)

## Full-text entities

- **Genes:** mTOR [NCBI Gene 100700382]
- **Diseases:** metabolic disorders (MESH:D008659)
- **Chemicals:** Cetobacterium (-), leucine (MESH:D007930), glucose (MESH:D005947), amino acid (MESH:D000596), lipid (MESH:D008055), TG (MESH:D014280), cholesterol (MESH:D002784)
- **Species:** Cetobacterium (genus) [taxon 180162], Tilapia (genus) [taxon 8126], Oreochromis niloticus (Nile tilapia, species) [taxon 8128]

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12858182/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12858182/full.md

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Source: https://tomesphere.com/paper/PMC12858182