Integrated physiological, transcriptomic, and metabolomic analyses provide new insights into hypoxia tolerance in large yellow croaker (Larimichthys crocea).
Aug 2026· Marine Pollution Bulletin· Vol 233 Pt 2, pp.
120275
· 0 citations· 49 references
Medicine
TL;DR
Multi-omics analysis revealed hypoxia-induced alterations in metabolites and genes, providing crucial insights into the hypoxia tolerance mechanism of the L. crocea and offering evidence supporting the improved hypoxia tolerance of the selected population.
Abstract
Owing to natural or anthropogenic factors, dissolved oxygen (DO) levels in aquatic environments frequently experience drastic fluctuations. Because fish are directly exposed to aquatic environments, DO fluctuations can disrupt physiological homeostasis, thereby inhibiting growth, reducing disease resistance, and potentially leading to mortality. To alleviate economic losses caused by hypoxia in Larimichthys crocea farming, we bred a novel strain with enhanced hypoxia tolerance. To elucidate the mechanisms underlying this enhanced tolerance, we conducted physiological, transcriptomic, and metabolomic analyses of both the hypoxia-tolerant (T) and control (N) groups under hypoxic stress to identify differentially expressed genes and metabolites. GO and KEGG enrichment analyses revealed that the T group adopted a more effective strategy when confronted with low oxygen levels, primarily by promoting glycolysis and the TCA cycle and enhancing the biosynthesis of carbohydrates, amino acids, terpenoids, and N-glycans. By contrast, the N group exhibited a relatively weaker glycolytic flux under hypoxic stress, with significant suppression of the tricarboxylic acid cycle and biosynthesis of energy-related substances and a greater reliance on oxygen-dependent lipid metabolism pathways. Overall, multi-omics analysis revealed hypoxia-induced alterations in metabolites and genes, providing crucial insights into the hypoxia tolerance mechanism of the L. crocea and offering evidence supporting the improved hypoxia tolerance of the selected population.
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Suitable dissolved oxygen levels are crucial for crustacean respiration and energy metabolism. To investigate the molecular mechanisms underlying hypoxia adaptation in the red swamp crayfish (
Procambarus clarkii
), we performed an integrated multi-omics analysis combining RNA-Seq transcriptomics and LC-MS non-targeted metabolomics on gill tissues under acute hypoxic (2.0±0.2 mg/L) and normoxic (7.5±0.2 mg/L) conditions. A total of 1,021 differentially expressed genes (DEGs) and 286 differentially expressed metabolites (DEMs) were identified. KEGG enrichment analysis revealed that DEGs were predominantly associated with lipid metabolism pathways, whereas DEMs were significantly enriched in nucleotide metabolism, purine metabolism, ABC transporter pathways and unsaturated fatty acid biosynthesis. Integrated transcriptomic and metabolomic analysis revealed 47 genes and 47 metabolites significantly associated across multiple key metabolic pathways, including lipid, carbohydrate, amino acid, and nucleotide metabolism. Specifically, genes associated with lipid synthesis and lipid degradation were upregulated, while the pentose phosphate pathway was activated to provide raw materials for fatty acid synthesis and produce NADPH to defend cell membranes from oxidative stress damage, indicating significant adjustments in energy metabolism pathways under hypoxic conditions. These findings provide a theoretical basis for deepening our understanding of hypoxic adaptation strategies in crustaceans. This multi-omics integration systematically revealed a coordinated metabolic reprogramming strategy in the gills of
P. clarkii
under acute hypoxia. These findings highlight the shift toward enhanced lipid turnover and NADPH production pathways (e.g., the pentose phosphate pathway) as key adaptive mechanisms, providing new insights into energy homeostasis and hypoxia tolerance in crustaceans beyond the traditional glycolysis-centered model.
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