{"title":"Integrated Transcriptomics and Metabolomics Unveil Key Regulators of Feed Efficiency in Larimichthys crocea on Fishmeal-Free Diets","authors":"Yuhan Jin, Gongsi Wang, Peng Ren, Lining Zhang, Qinghui Ai, Yunzhang Sun, Fang Han, Zhiyong Wang","doi":"10.1155/anu/2147842","DOIUrl":null,"url":null,"abstract":"<div>\n <p>Understanding the molecular underpinnings of feed efficiency (FE) is crucial for advancing sustainable aquaculture, particularly under fishmeal-free (FM-free) dietary strategies. This study investigated the physiological, transcriptomic, and metabolomic differences between high-FE and low-FE <i>Larimichthys crocea</i> individuals fed a plant-based diet. High-FE fish exhibited significantly higher activities of hepatic amylase (AMS), hepatic lipase (HL), and lipoprotein lipase (LPL), as well as changed serum albumin (ALB) and peroxidase (POD) levels, suggesting enhanced digestive function and antioxidant capacity. Transcriptomic analysis revealed 239 differentially expressed genes (DEGs), with significant enrichment in steroid biosynthesis, ribosome biogenesis, and autophagy pathways. Genes involved in glycolysis were downregulated, indicating a metabolic shift toward increased reliance on lipid and protein catabolism. Metabolomic profiling identified 359 differentially expressed metabolites (DEMs), primarily comprising lipids and amino acids, enriched in pathways related to amino acid metabolism, energy production, and ABC transporter activity. Integrative O2PLS and correlation analyses identified tightly linked gene–metabolite pairs, such as <i>pfkp</i> and peptide fragment, and highlighted <i>mao</i> as a regulatory factor that links energy and protein digestion. Protein–protein interaction (PPI) analysis identified five hub genes (<i>tpi1</i>, <i>tktl2</i>, <i>fdps</i>, <i>pgam1</i>, and <i>ldha</i>) that are central to metabolic coordination. These findings offer comprehensive insights into the metabolic reprograming and regulatory mechanisms underlying enhanced FE in <i>L. crocea</i>, highlighting potential molecular targets for selective breeding and feed optimization in FM-free aquaculture systems.</p>\n </div>","PeriodicalId":8225,"journal":{"name":"Aquaculture Nutrition","volume":"2025 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/anu/2147842","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquaculture Nutrition","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1155/anu/2147842","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0
Abstract
Understanding the molecular underpinnings of feed efficiency (FE) is crucial for advancing sustainable aquaculture, particularly under fishmeal-free (FM-free) dietary strategies. This study investigated the physiological, transcriptomic, and metabolomic differences between high-FE and low-FE Larimichthys crocea individuals fed a plant-based diet. High-FE fish exhibited significantly higher activities of hepatic amylase (AMS), hepatic lipase (HL), and lipoprotein lipase (LPL), as well as changed serum albumin (ALB) and peroxidase (POD) levels, suggesting enhanced digestive function and antioxidant capacity. Transcriptomic analysis revealed 239 differentially expressed genes (DEGs), with significant enrichment in steroid biosynthesis, ribosome biogenesis, and autophagy pathways. Genes involved in glycolysis were downregulated, indicating a metabolic shift toward increased reliance on lipid and protein catabolism. Metabolomic profiling identified 359 differentially expressed metabolites (DEMs), primarily comprising lipids and amino acids, enriched in pathways related to amino acid metabolism, energy production, and ABC transporter activity. Integrative O2PLS and correlation analyses identified tightly linked gene–metabolite pairs, such as pfkp and peptide fragment, and highlighted mao as a regulatory factor that links energy and protein digestion. Protein–protein interaction (PPI) analysis identified five hub genes (tpi1, tktl2, fdps, pgam1, and ldha) that are central to metabolic coordination. These findings offer comprehensive insights into the metabolic reprograming and regulatory mechanisms underlying enhanced FE in L. crocea, highlighting potential molecular targets for selective breeding and feed optimization in FM-free aquaculture systems.
期刊介绍:
Aquaculture Nutrition is published on a bimonthly basis, providing a global perspective on the nutrition of all cultivated aquatic animals. Topics range from extensive aquaculture to laboratory studies of nutritional biochemistry and physiology. The Journal specifically seeks to improve our understanding of the nutrition of aquacultured species through the provision of an international forum for the presentation of reviews and original research papers.
Aquaculture Nutrition publishes papers which strive to:
increase basic knowledge of the nutrition of aquacultured species and elevate the standards of published aquaculture nutrition research.
improve understanding of the relationships between nutrition and the environmental impact of aquaculture.
increase understanding of the relationships between nutrition and processing, product quality, and the consumer.
help aquaculturalists improve their management and understanding of the complex discipline of nutrition.
help the aquaculture feed industry by providing a focus for relevant information, techniques, tools and concepts.