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添加酵母固态发酵产物对鲤鱼肝脏和肠道健康以及鲤鱼抗鲤春病毒血症病毒能力的影响。

Effects of solid-state fermentation product of yeast supplementation on liver and intestinal health, and resistance of common carp () against spring viraemia carp virus.

作者信息

Wang Mengxin, Xia Dongmei, Yu Lijuan, Hao Qiang, Xie Mingxu, Zhang Qingshuang, Zhao Yajie, Meng Delong, Yang Yalin, Ran Chao, Teame Tsegay, Zhang Zhen, Zhou Zhigang

机构信息

China-Norway Joint Lab on Fish Gut Microbiota, Institute of Feed Research, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University, Wuhan 430000, China.

出版信息

Anim Nutr. 2024 Jun 3;18:408-418. doi: 10.1016/j.aninu.2024.04.017. eCollection 2024 Sep.

DOI:10.1016/j.aninu.2024.04.017
PMID:39309973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11415639/
Abstract

This study aimed to investigate the effects of solid-state fermentation products of yeast (SFPY) on liver and intestinal health and disease resistance of common carp (). A total of 200 common carp with an initial average weight of 2.55 ± 0.004 g were divided into 5 groups (4 replications per group and 10 fish per replication), and were fed with one of five diets, including a control diet and 4 diets supplemented with 2‰ (Y2), 3‰ (Y3), 4‰ (Y4), or 5‰ (Y5) SFPY, respectively, for 8 weeks. Results indicated that, the addition of SFPY to the diet of common carp did not affect the growth performance or survival rate of fish ( = 0.253). Interestingly, with the addition of SFPY, the triacylglycerol (TAG) content of the liver presented a linear decreasing tendency ( = 0.004), with significantly decreased in Y4 and Y5 groups ( = 0.035) compared with control. Serum lipopolysaccharide (LPS) content and diamine oxidase (DAO) activity presented a negative linear relationship with the addition of SFPY ( = 0.015,  = 0.030), while serum lipopolysaccharide binding protein (LBP) content first decreased and then increased ( < 0.001). The total antioxidant capacity (T-AOC) in the intestine of fish increased continuously with increasing SFPY supplementation ( = 0.026), reaching the highest level in Y5 group. The villus height in all experimental groups were significantly higher than that in the control group ( < 0.001). Furthermore, compared to the control, adding 3‰ SFPY to the control diet of common carp significantly increased the relative abundance of Fusobacteria ( = 0.018) and decreased that of Proteobacteria ( = 0.039) at phylum level, and increased the relative abundance of (= 0.018) and decreased that of ( = 0.013) at genus level. Compared with the control, the relative mRNA expression level of spring viraemia of carp virus N protein ( ) in the kidney was lower than that of the control group without significance and bottomed out in Y4 group ( = 0.138). In conclusion, dietary SFPY enhanced the SVCV resistance capacity of common carp by improving liver and intestinal health and modulating the gut microbiota. Thus, SFPY is a potential feed additive to be used in aquaculture to reduce the huge economic loss of common carp due to SVCV disease. Based on liver TAG content and intestinal villus height, the optimal addition level of SFPY was 3.02‰ and 2.72‰, respectively.

摘要

本研究旨在探讨酵母固态发酵产物(SFPY)对鲤鱼肝脏和肠道健康以及抗病能力的影响。选取初始平均体重为2.55±0.004 g的200尾鲤鱼,分为5组(每组4个重复,每个重复10尾鱼),分别投喂5种饲料中的一种,包括对照饲料和添加2‰(Y2)、3‰(Y3)、4‰(Y4)或5‰(Y5)SFPY的4种饲料,为期8周。结果表明,在鲤鱼饲料中添加SFPY对鱼的生长性能或存活率没有影响(P = 0.253)。有趣的是,随着SFPY的添加,肝脏中三酰甘油(TAG)含量呈线性下降趋势(P = 0.004),Y4组和Y5组与对照组相比显著降低(P = 0.035)。血清脂多糖(LPS)含量和二胺氧化酶(DAO)活性与SFPY的添加呈负线性关系(P = 0.015,P = 0.030),而血清脂多糖结合蛋白(LBP)含量先下降后上升(P < 0.001)。随着SFPY添加量的增加,鱼肠道中的总抗氧化能力(T-AOC)持续升高(P = 0.026),在Y5组达到最高水平。所有实验组的绒毛高度均显著高于对照组(P < 0.001)。此外,与对照组相比,在鲤鱼对照饲料中添加3‰ SFPY在门水平上显著增加了梭杆菌的相对丰度(P = 0.018),降低了变形菌门的相对丰度(P = 0.039),在属水平上增加了某属的相对丰度(P = 0.018)并降低了另一属的相对丰度(P = 0.013)。与对照组相比,肾脏中鲤鱼春季病毒血症病毒N蛋白()的相对mRNA表达水平低于对照组但无显著差异,在Y4组降至最低(P = 0.138)。总之,日粮SFPY通过改善肝脏和肠道健康以及调节肠道微生物群来增强鲤鱼对鲤春病毒血症病毒(SVCV)的抵抗能力。因此,SFPY是一种潜在的饲料添加剂,可用于水产养殖,以减少鲤鱼因SVCV疾病造成的巨大经济损失。基于肝脏TAG含量和肠道绒毛高度,SFPY的最佳添加水平分别为3.02‰和2.72‰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/0c3e837f5a3b/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/75c6f4d54910/gr1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/5acabb020001/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/9ae09d087e71/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/8c32644628c4/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/eb40bea747c9/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/0c3e837f5a3b/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/75c6f4d54910/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/328a45cc223d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/5acabb020001/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/9ae09d087e71/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/8c32644628c4/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/11415639/eb40bea747c9/gr6.jpg
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