Reparative effect of different dietary additives on soybean meal-induced intestinal injury in yellow drum (Nibea albiflora).

Soybean meal (SBM) is an acceptable replacement for unsustainable marine fish meal (FM) in aquaculture. However, we previously reported that high dietary SBM supplementation causes intestinal inflammatory injury in yellow drum (Nibea albiflora). Accordingly, a 4-week SBM-induced enteritis (SBMIE) in yellow drum trial was conducted first, followed by a 4-week additive-supplemented reparative experiment to evaluate the reparative effect of five additives on SBMIE in yellow drum. The control diet comprised 50% FM protein substituted with SBM. The additive-supplemented diet was added with 0.02% curcumin (SBMC), 0.05% berberine (SBM-BBR), 0.5% tea polyphenols (SBM-TPS), 1% taurine (SBM-TAU), or 0.8% glutamine (SBM-GLU) based on the control diet, respectively. The weight gain (WG), specific growth rate (SGR), feed efficiency ratio (FER), and survival rate (SR) of fish fed the additive-supplemented diets were significantly higher than those of fish fed the SBM diet. The WG, SGR, and FER of fish fed the SBMC, SBM-GLU and SBM-TAU diets were significantly higher than those of fish fed other diets. Moreover, fish fed the additive-supplemented diets SBMC and SBM-GLU, exhibited significantly increased intestinal villus height (IVH), intestinal muscular thickness (IMRT), and intestinal mucosal thickness (IMLT) and significantly decreased crypt depth (CD) in comparison with those fed the SBM diets. The relative expression of intestinal tight junction factors (ocln, zo1), cytoskeletal factors (f-actin, arp2/3), and anti-inflammatory cytokines (il10, tgfb) mRNA was remarkably elevated in fish fed additive-supplemented diets than those of fish fed the SBM diet. Whereas, the relative expression of intestinal myosin light chain kinase (mlck) and pro-inflammatory cytokines (il1, il6, tnfa) mRNA was markedly lower in fish fed the additive-supplemented diets. The highest relative expression of intestinal ocln, f-actin, and arp2/3 and the lowest relative expression of intestinal mlck were found in fish fed the SBMC diet. Hence, all five dietary additives effectively repaired the intestinal injury induced by SBM, with curcumin exhibiting the strongest repair effect for SBMIE in yellow drum.

iTRAQ-based quantitative phosphoproteomics provides insights into the metabolic and physiological responses of a carnivorous marine fish (Nibea albiflora) fed a linseed oil-rich diet.

The limited production of fish oil (FO) cannot meet the increasing demand of the aqua-feed industry. Accordingly, the replacement of FO with sustainable alternatives such as vegetable oils has become imperative. Linseed oil (LO), which has an abundance of α-linolenic acid (ALA), is a promising FO alternative. Nevertheless, high dietary LO inclusion generally causes abnormal hepatic lipid accumulation and growth retardation across carnivorous marine fish species. Previous studies have attempted to elucidate the mechanisms with regard to gene and protein levels; however, little is known about posttranslational modifications. In the present study, iTRAQ phosphoproteomics was conducted to investigate the metabolic and physiological responses of the yellow drum (Nibea albiflora) fed an LO-rich or FO-rich diet. Identification and analyses of differentially abundant phosphorylated proteins in hepatic tissue were conducted with parallel reaction monitoring (PRM) verification in reference to the genome sequences of the yellow drum. Among the specific peptides that passed the threshold, 203 hyperphosphorylated and 182 hypophosphorylated peptides were identified. Several functional categories and pathways were associated with these proteins that were mostly related to lipid, amino acid, and carbohydrate metabolism. In particular, the AMP-activated protein kinase (AMPK) pathway, mechanistic target of rapamycin (mTOR) pathway, and citrate (TCA) cycle are discussed. STATEMENT OF SIGNIFICANCE: Dietary LO caused abnormal hepatic lipid accumulation and retarded growth performance. The abnormal hepatic lipid accumulation in the fish fed the LO-rich diet might have arisen from AMPK signaling pathway-mediated de novo synthesis of fatty acids and the synthesis of phospholipids. An mTOR signaling pathway-mediated reduction in ribosome protein synthesis could have been a factor in the growth retardation. Changes in UPS and autophagy proteins phosphorylation and aminotransferase activity levels were related to the flux of amino acids into the TCA cycle for ATP production. The results of PRM were highly correlated with the phosphoproteomics results. These findings will contribute to a better understanding of the mechanisms of abnormal hepatic lipid accumulation and retarded growth performance in carnivorous marine fish fed linseed oil-rich diets.

Molecular Cloning, Characterization, and mRNA Expression of Hemocyanin Subunit in Oriental River Prawn Macrobrachium nipponense.

Hemocyanin is a copper-containing protein with immune function against disease. In this study, a hemocyanin subunit named MnHc-1 was cloned from Macrobrachium nipponense. The full-length cDNA of MnHc-1 was 2,163 bp with a 2,028-bp open reading frame (ORF) encoding a polypeptide of 675 amino acids. The MnHc-1 mRNA was expressed in the hepatopancreas, gill, hemocytes, intestine, ovary, and stomach, with the highest level in the hepatopancreas. In the infection trial, the MnHc-1 mRNA transcripts in the hemocytes were significantly downregulated at 3 h after injection of Aeromonas hydrophila and then upregulated at 6 h and 12 h, followed by a gradual recovery from 24 to 48 h. The MnHc-1 transcriptional expression in the hepatopancreas was measured after M. nipponense were fed seven diets with 2.8, 12.2, 20.9, 29.8, 43.1, 78.9, and 157.1 mg Cu kg-1 for 8 weeks, respectively. The level of MnHc-1 mRNA was significantly higher in the prawns fed 43.1-157.1 mg Cu kg-1 diet than in that fed 2.8-29.8 mg Cu kg-1 diet. This study indicated that the MnHc-1 expression can be affected by dietary copper and the hemocyanin may potentially participate in the antibacterial defense of M. nipponense.