No abstract

A 10-week feeding trial was conducted to evaluate the effects of dietary lipid sources on the growth and immune responses of Chinese mitten crab Eriocheir sinensis. Six isonitrogenous and isoenergetic diets were formulated with fish oil (FO), linseed oil (LO), soybean oil (SO), rapeseed oil (RO), coconut oil (CO) and beef tallow (BT) as the sources of lipid with five replicates each. Thirty crabs (2.35 AE 0.14 g) were stocked into each tank and fed twice daily. Weight gain and specific growth rate of crab fed the FO diet were significantly lower than those fed other diets (P < 0.05), except for crabs fed LO diet (P < 0.05). Crab fed the SO diet weighed more than those fed FO diets (P < 0.05). Serum superoxide dismutase and malondialdehyde of crab fed the FO diet were significantly higher than in other groups (P < 0.05). Crab fed the FO diet had the highest activities of serum phenoloxidase, acid phosphatase, alkaline phosphatase and lysozyme (P < 0.05). The fatty acid composition in the liver of crab reflected the change in test diets. Our results indicate that the use of dietary vegetable or animal oils can achieve similar growth performance to the use of dietary FO in Chinese mitten crab, but non-FOs may impair crab immunity. Soybean oil is recommended as a suitable replacer for FO in Chinese mitten crab diet.

The role of dietary linolenic acid (LN), vitamin E (E) and vitamin C (C) in regulating fish growth and immune response was tested on juvenile darkbarbel catfish Pelteobagrus vachelli. Five dietary combinations were used (−E−LN, +E−LN, −E+LN, +E+LN and −C+E+LN; ‘+’ with addition and ‘−’ without addition) in triplicate. Weight gain was highest in the −E+LN feeding group. Red blood cell in fish fed the +E+LN diet was highest. The haematocrit and haemoglobin of fish fed the −E+LN diet was lowest. Superoxide dismutase, catalase, glutathione peroxidase and glucose‐6‐phosphate dehydrogenase activities in fish fed the −E+LN diet were higher than those in fish fed other diets. Malondialdehyde in fish fed the −C+E+LN diet was highest. Fish fed the +E+LN diet had higher levels of lysozyme activity, serum protein, complements C3 and C4, and immunoglobulin contents than fish fed other diets. Fish fed the +E+LN diet showed lower mortality and higher antibody titre than fish fed other diets after the fish were challenged with Aeromonas hydrophila for 14 day. This study suggests that the growth of darkbabel catfish is improved by increasing dietary linolenic acids. The diets with high linolenic acid, vitamin E and vitamin C can enhance the immune response and resistance in darkbarbel catfish challenged with A. hydrophila.

Six purified diets were formulated to contain three lipid sources, fish oil (FO), linseed oil (LO) and soybean oil (SO), at 6% diet lipid crossing two levels of vitamin E (100 and 300 mg α‐tocopheryl acetate/kg diet) for each lipid source (FO100, FO300, LO100, LO300, SO100, SO300). The juvenile Chinese mitten crab, Eriocheir sinensis, respectively, fed on these diets with four replicates for 6 weeks. The crab weight gain (WG) and specific growth rate (SGR) were significantly affected by dietary lipid sources. No difference was found between the crabs fed two levels of vitamin E, but the WG and SGR were numerically higher in crab fed 300 mg/kg vitamin E than those fed the other level of vitamin E. The lipid source and vitamin E level could affect fatty acid composition in the hepatopancreas. The contents of saturated fatty acids (SAFA) and n‐3HUFA were significantly higher in the crab‐fed fish oil. The highest contents of n‐6PUFA and n‐3PUFA were found in the crab‐fed soybean oil and linseed oil respectively. The contents of SAFA, n‐3HUFA and n‐3PUFA were higher in the 300 mg/kg vitamin E treatment. A lower malondialdehyde (MDA) content and higher phenoloxidase (PO) activity were observed in the crab fed 300 mg/kg vitamin E. The results of this study indicate that the Chinese mitten crab fed the diet with 6% fish oil and 300 mg/kg vitamin E showed better growth, antioxidant capacity and resistance to Aeromonas hydrophila.