元基因组和代谢组的综合分析为通过益生菌干预保护鲚幼虫肠道健康提供了新见解

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology D-Genomics & Proteomics Pub Date : 2024-04-06 DOI:10.1016/j.cbd.2024.101230
Qi Mang , Jun Gao , Quanjie Li , Yi Sun , Gangchun Xu , Pao Xu
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摘要

随着大规模集约化饲养的发展,生长性能和动物福利越来越受到关注。外源性益生菌可以通过改善肠道微生物群来促进鱼类的生长性能;然而,肠道微生物群是否会影响生理生物标志物仍不清楚。因此,我们进行了元基因组和代谢组分析,研究在基础日粮(1.0 × 108 CFU/g)中添加植物乳杆菌(Lactiplantibacillus plantarum)90天对鲚幼鱼生长性能、肠道微生物群及其代谢产物和生理生物标志物的影响。结果表明,补充益生菌可显著增加体重和体长。此外,益生菌还能增强消化酶和紧密连接,抑制氧化应激和炎症。元基因组分析表明,补充植物乳杆菌可显著降低蛋白菌的相对丰度,提高固缩菌的相对丰度。此外,致病菌(气单胞菌科、气单胞菌属和肠杆菌科)受到抑制,有益菌(芽孢杆菌科)得到促进。代谢组分析表明,醋酸和丙酸明显升高,并与 Kitasatospora、Seonamhaeicola 和 Thauera 相关。相关性分析表明,消化酶、紧密连接、氧化应激和炎症效应与乙酸和丙酸水平的升高显著相关。这些结果表明,补充植物乳杆菌可改善肠道微生物群落结构和功能,从而提高乙酸和丙酸水平,保护鼻疽幼虫的肠道健康并改善其生长性能。
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Integrative analysis of metagenome and metabolome provides new insights into intestinal health protection in Coilia nasus larvae via probiotic intervention

With the development of large-scale intensive feeding, growth performance and animal welfare have attracted more and more attention. Exogenous probiotics can promote the growth performance of fish through improving intestinal microbiota; however, it remains unclear whether intestinal microbiota influence physiological biomarkers. Therefore, we performed metagenomic and metabolomic analysis to investigate the effects of a 90-day Lactiplantibacillus plantarum supplementation to a basal diet (1.0 × 108 CFU/g) on the growth performance, intestinal microbiota and their metabolites, and physiological biomarkers in Coilia nasus larvae. The results showed that the probiotic supplementation could significantly increase weight and body length. Moreover, it could also enhance digestive enzymes and tight junctions, and inhibit oxidative stress and inflammation. The metagenomic analysis showed that L. plantarum supplementation could significantly decrease the relative abundance of Proteobacteria and increase the relative abundance of Firmicutes. Additionally, pathogenic bacteria (Aeromonadaceae, Aeromonas, and Enterobacterales) were inhibited and beneficial bacteria (Bacillales) were promoted. The metabolome analysis showed that acetic acid and propanoic acid were significantly elevated, and were associated with Kitasatospora, Seonamhaeicola, and Thauera. A correlation analysis demonstrated that the digestive enzymes, tight junction, oxidative stress, and inflammation effects were significantly associated with the increased acetic acid and propanoic acid levels. These results indicated that L. plantarum supplementation could improve intestinal microbial community structure and function, which could raise acetic acid and propanoic acid levels to protect intestinal health and improve growth performance in C. nasus larvae.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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