Artemia Nauplii Enriched with Soybean Lecithin Enhances Growth Performance, Intestine Morphology, and Desiccation Stress Resistance in Yellow Drum (Nibea albiflora) Larvae.

IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Metabolites Pub Date : 2025-01-17 DOI:10.3390/metabo15010063
Zhenya Zhou, Pian Zhang, Peng Tan, Ruiyi Chen, Weihua Hu, Ligai Wang, Yuming Zhang, Dongdong Xu
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Abstract

The inherent deficiency of phospholipids in Artemia limits its nutritional value as live prey for marine fish larvae. In our previous study, we optimized a phospholipid enrichment method by incubating Artemia nauplii with 10 g of soybean lecithin per m3 of seawater for 12 h, significantly enhancing their phospholipid content. Purpose: The present study evaluated the impact of this enrichment on yellow drum (Nibea albiflora) larvae, focusing on growth performance, intestinal morphology, body composition, weaning success, and desiccation stress resistance. Methods: The larvae (12 days post-hatching, dph) were fed either soybean lecithin-enriched (SL group) or newly hatched (NH group) Artemia nauplii for 10 days. Results: By the end of the experiment, the SL group exhibited a markedly greater body weight and standard length compared to the NH group (p < 0.05). This growth improvement was due to enhanced intestinal morphology, characterized by a significantly higher mucosal fold height, microvillus density, and microvillus length (p < 0.05). Intestinal RNA sequencing identified 160 upregulated and 447 downregulated differentially expressed genes (DEGs) in the SL group compared to the NH group. Soybean lecithin enrichment reduced the expression of lipogenesis-related genes (fasn, scd, elovl1) while upregulating lipid catabolism genes (ppara, cpt1, cpt2), indicating increased lipid breakdown and energy production. After a 5-day weaning period onto a commercial microdiet, the SL group continued to show significantly superior growth performance. In an afterward desiccation stress test, larvae from the SL group demonstrated significantly higher survival rates, potentially due to the decreased expression of intestinal cytokine genes (ccl13, mhc1, mhc2) observed in the RNA-seq analysis. Conclusions: This study highlights that feeding soybean lecithin-enriched Artemia nauplii enhances growth performance and desiccation stress in yellow drum larvae by promoting lipid catabolism, improving intestinal structure, and regulating immune responses.

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添加大豆卵磷脂可提高黄鼓(Nibea albiflora)幼虫的生长性能、肠道形态和干燥胁迫抗性。
青蒿本身缺乏磷脂,限制了其作为海鱼幼虫活食的营养价值。在我们之前的研究中,我们优化了一种磷脂富集方法,将10 g大豆卵磷脂/ m3海水培养12 h,显著提高了青蒿的磷脂含量。目的:本研究评估了这种富集对黄鼓(Nibea albiflora)幼虫的影响,重点研究了生长性能、肠道形态、体组成、断奶成功率和干燥胁迫抗性。方法:幼虫(孵化后12 d, dph)分别饲喂大豆卵磷脂富集组(SL组)和新孵化组(NH组)10 d。结果:实验结束时,SL组的体重和标准体长明显高于NH组(p < 0.05)。这种生长改善是由于肠道形态的增强,其特征是粘膜褶皱高度、微绒毛密度和微绒毛长度显著增加(p < 0.05)。肠道RNA测序发现,与NH组相比,SL组有160个差异表达基因(DEGs)上调,447个差异表达基因(DEGs)下调。大豆卵磷脂的富集降低了脂肪生成相关基因(fasn、scd、elovl1)的表达,同时上调了脂质分解代谢基因(ppara、cpt1、cpt2),表明脂质分解和能量产生增加。断奶5天后,SL组继续表现出显著优越的生长性能。在随后的干燥应激测试中,SL组的幼虫表现出明显更高的存活率,可能是由于在RNA-seq分析中观察到肠道细胞因子基因(ccl13, mhc1, mhc2)的表达降低。结论:本研究提示,饲喂富含大豆卵磷脂的黄颡鱼幼虫可通过促进脂质分解代谢、改善肠道结构和调节免疫应答等方式改善黄颡鱼幼虫的生长性能和干燥应激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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