Intestinal transcriptome analysis reveals enrichment of genes associated with immune and lipid mechanisms, favoring soybean meal tolerance in high-growth zebrafish (Danio Rerio)
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2021Metadata
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Valenzuela, Luis
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Intestinal transcriptome analysis reveals enrichment of genes associated with immune and lipid mechanisms, favoring soybean meal tolerance in high-growth zebrafish (Danio Rerio)
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Abstract
The molecular mechanisms underlying fish tolerance to soybean meal (SBM) remain unclear.
Identifying these mechanisms would be beneficial, as this trait favors growth. Two fish replicates
from 19 experimental families were fed fishmeal-(100FM) or SBM-based diets supplemented with
saponin (50SBM + 2SPN) from juvenile to adult stages. Individuals were selected from families
with a genotype-by-environment interaction higher (HG-50SBM + 2SPN, 170 18 mg) or lower
(LG-50SBM + 2SPN, 76 10 mg) weight gain on 50SBM + 2SPN for intestinal transcriptomic
analysis. A histological evaluation confirmed middle intestinal inflammation in the LG- vs. HG-
50SBM + 2SPN group. Enrichment analysis of 665 differentially expressed genes (DEGs) identified
pathways associated with immunity and lipid metabolism. Genes linked to intestinal immunity
were downregulated in HG fish (mpx, cxcr3.2, cftr, irg1l, itln2, sgk1, nup61l, il22), likely dampening
inflammatory responses. Conversely, genes involved in retinol signaling were upregulated (rbp4,
stra6, nr2f5), potentially favoring growth by suppressing insulin responses. Genes associated with
lipid metabolism were upregulated, including key components of the SREBP (mbtps1, elov5l, elov6l)
and cholesterol catabolism (cyp46a1), as well as the downregulation of cyp7a1. These results strongly
suggest that transcriptomic changes in lipid metabolism mediate SBM tolerance. Genotypic variations
in DEGs may become biomarkers for improving early selection of fish tolerant to SMB or others
plant-based diets.
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Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)
CONICYT FONDECYT 11170847
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Artículo de publícación WoS Artículo de publicación SCOPUS
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Genes 2021, 12, 700
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