The direct and gut microbiota-mediated effects of dietary bile acids on the improvement of gut barriers in largemouth bass (Micropterus salmoides)

IF 6.3 Animal Nutrition Pub Date : 2023-09-01 DOI:10.1016/j.aninu.2023.03.008
Rui Xia , Qingshuang Zhang , Dongmei Xia , Qiang Hao , Qianwen Ding , Chao Ran , Yalin Yang , Aizhi Cao , Zhen Zhang , Zhigang Zhou
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引用次数: 1

Abstract

Fish gut barrier damage under intensive culture model is a significant concern for aquaculture industry. This study aimed to investigate the effects of bile acids (BAs) on gut barriers in Micropterus salmoides. A germ-free (GF) zebrafish model was employed to elucidate the effects of the direct stimulation of BAs and the indirect regulations mediated by the gut microbiota on gut barrier functions. Four diets were formulated with BAs supplemented at 0, 150, 300 and 450 mg/kg, and these 4 diets were defined as control, BA150, BA300 and BA450, respectively. After 5 weeks of feeding experiment, the survival rate of fish fed with BA300 diet was increased (P < 0.05). Histological analysis revealed an improvement of gut structural integrity in the BA150 and BA300 groups. Compared with the control group, the expression of genes related to chemical barrier (mucin, lysozyme and complement 1) and physical barrier (occludin and claudin-4) was increased in the BA150 and BA300 groups (P < 0.05), and the expression of genes related to immunological barrier (interleukin [IL]-6, tumor growth factor β, IL-10, macrophage galactose-type lectin and immunoglobulin M [IgM]) was significantly increased in the BA300 group (P < 0.05), but the expression of genes related to chemical barrier (hepcidin) and immunological barrier (IL-1β, tumor necrosis factor, IL-6 and arginase) was significantly decreased in the BA450 group (P < 0.05). Gut microbiota composition analysis revealed that the abundance of Firmicutes was augmented prominently in the BA150 and BA300 groups (P < 0.05), while that of Actinobacteriota and Proteobacteria showed a downward trend in the BA150 and BA300 groups (P > 0.05). The results of the gut microbiota transferring experiment demonstrated an upregulation of gut barrier-related genes, including immunoglobulin Z/T (IgZ/T), IL-6, IL-1β and IL-10, by the gut microbiota transferred from the BA300 group compared with the control (P < 0.05). Feeding the BA300 diet directly to GF zebrafish resulted in enhanced expression of IgM, IgZ/T, lysozyme, occludin-2, IL-6 and IL-10 (P < 0.05). In conclusion, BAs can improve the gut barriers of fish through both direct and indirect effects mediated by the gut microbiota.

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饮食胆汁酸对改善大口鲈鱼肠道屏障的直接和肠道微生物群介导作用
集约养殖模式下的鱼类肠道屏障损伤是水产养殖业关注的一个重要问题。本研究旨在研究胆汁酸(BAs)对微小筛管肠道屏障的影响。采用无菌(GF)斑马鱼模型来阐明BA的直接刺激和肠道微生物群介导的间接调节对肠道屏障功能的影响。用0、150、300和450 mg/kg的BA配制了四种日粮,并将这4种日粮分别定义为对照、BA150、BA300和BA450。经过5周的饲养实验,用BA300饲料喂养的鱼的存活率提高(P<;0.05)。组织学分析显示,BA150和BA300组的肠道结构完整性有所改善。与对照组相比,BA150和BA300组与化学屏障(粘蛋白、溶菌酶和补体1)和物理屏障(occludin和claudin-4)相关的基因表达增加(P<;0.05),BA300组免疫屏障相关基因(白细胞介素[IL]-6、肿瘤生长因子β、IL-10、巨噬细胞半乳糖型凝集素和免疫球蛋白M[IgM])的表达显著增加(P<;0.05),但与化学屏障(铁调素)和免疫屏障(IL-1β、肿瘤坏死因子-α、IL-6和精氨酸酶)相关的基因在BA450组中的表达显著降低(P<;0.05),而放线菌和变形菌在BA150和BA300组中表现出下降趋势(P>;0.05)。肠道微生物群转移实验的结果表明,肠道屏障相关基因上调,包括免疫球蛋白Z/T(IgZ/T)、IL-6、IL-1β和IL-10,与对照组相比(P<;0.05)。将BA300日粮直接饲喂GF斑马鱼可增强IgM、IgZ/T、溶菌酶、occludin-2、IL-6和IL-10的表达(P<)。总之,BAs可通过肠道微生物群介导的直接和间接作用改善鱼类的肠道屏障。
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来源期刊
Animal Nutrition
Animal Nutrition Animal Science and Zoology
CiteScore
9.70
自引率
0.00%
发文量
542
审稿时长
65 days
期刊介绍: Animal Nutrition encompasses the full gamut of animal nutritional sciences and reviews including, but not limited to, fundamental aspects of animal nutrition such as nutritional requirements, metabolic studies, body composition, energetics, immunology, neuroscience, microbiology, genetics and molecular and cell biology related to primarily to the nutrition of farm animals and aquatic species. More applied aspects of animal nutrition, such as the evaluation of novel ingredients, feed additives and feed safety will also be considered but it is expected that such studies will have a strong nutritional focus. Animal Nutrition is indexed in SCIE, PubMed Central, Scopus, DOAJ, etc.
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