CHEN Xun, HAN Dong, LUO Zuo-Yong, ZHANG Yue-Xing, ZHANG Zhi-Min, LIU Hao-Kun, JIN Jun-Yan, YANG Yun-Xia, ZHU Xiao-Ming, XIE Shou-Qi. DIETARY YEAST CULTURE ON GROWTH, INTESTINAL HEALTH AND IMMUNITY OF MICROPTERUS SALMOIDES[J]. ACTA HYDROBIOLOGICA SINICA, 2024, 48(1): 23-33. DOI: 10.7541/2023.2023.0080
Citation: CHEN Xun, HAN Dong, LUO Zuo-Yong, ZHANG Yue-Xing, ZHANG Zhi-Min, LIU Hao-Kun, JIN Jun-Yan, YANG Yun-Xia, ZHU Xiao-Ming, XIE Shou-Qi. DIETARY YEAST CULTURE ON GROWTH, INTESTINAL HEALTH AND IMMUNITY OF MICROPTERUS SALMOIDES[J]. ACTA HYDROBIOLOGICA SINICA, 2024, 48(1): 23-33. DOI: 10.7541/2023.2023.0080

DIETARY YEAST CULTURE ON GROWTH, INTESTINAL HEALTH AND IMMUNITY OF MICROPTERUS SALMOIDES

  • Yeast culture is a micro-ecological product formed by anaerobic fermentation of yeast, containing a variety of active substances. In order to investigate the effects of yeast culture supplementation on growth performance, intestinal health, immunity and cumulative survival rate after bacteria challenge in largemouth bass (Micropterus salmoides), 1 g/kg (S1 diet) and 3 g/kg (S2 diet) of yeast culture supplementation were added to the control diet (Con diet), respectively. The three experimental diets were formulated with the same nutritional contents of protein (52%) and lipid (8.5%). The growth experiment was conducted in the pond cage (the size of 2 m×2 m×2 m). The 360 largemouth bass with the similar initial body weight of (32.37±0.15) g were divided into 3 dietary treatments, each with 3 replicates cages. 40 fish were stocked in each cage, and the growth experiment period was 11 weeks. At the end of growth experiment, the samples were taken from each cages 7h after the last feeding. The results showed that the final body weight (FBW), weight gain rate (WGR) and specific growth rate (SGR) of supplemented yeast culture groups had no significant difference compared with the control group (P>0.05). The condition factor (CF), hepatosomatic index (HSI) of supplemented yeast culture groups had no significant difference compared with the control group (P>0.05), while S2 group had the lowest value of HSI. In terms of intestinal structure, the villus length of S2 group and the depth of crypts were significantly increased compared with the control group (P<0.05). For intestinal microbes, S1 and S2 group both reduced the contents of Cyanobacteria and Staphylococcus in the intestine and increased the intestinal content of Clostridiales compared with the control group. The activities of head kidney superoxide dismutase (SOD), catalase (CAT), alkaline phosphatase (AKP) and lysozyme (LZM) in S2 group increased significantly (P<0.05) compared to the control group. The contents of head kidney malondialdehyde (MDA) in yeast culture supplementation groups showed no significant difference compared with the control group (P>0.05). The S1 group significantly increased the activity of plasma SOD (P<0.05) and S2 group significantly reduced the plasma malondialdehyde (MDA) content (P<0.05) compared to the control group. The yeast culture supplementation group increased the plasma lysozyme activities compared to the control group and showed no significant difference (P>0.05). The cumulative survival rate of S1 and S2 groups was significantly higher than that of the control group after 252h changed with Aeromonas hydrophila (P<0.05). The results indicated that dietary supplementation of 0.1%—0.3% yeast culture had positive effects on intestinal health, antioxidant capacity, immunity and disease resistance in largemouth bass.
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