热带桡足类Apocyclops royi-TH对盐度胁迫反应的多组学研究:对免疫和多不饱和脂肪酸生物合成的影响

IF 2.4 3区 农林科学 Q1 FISHERIES
Nutthawan Thepsoonthorn , Supida Kueakob , Natkanokporn Prayoonmaneerat , Piti Amparyup , Walaiporn Charoensapsri , Chanprapa Imjongjirak
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引用次数: 0

摘要

盐度是影响水生生物生物过程的关键环境因子。Apocyclops royi-TH是一种原产于泰国的桡足类动物,具有很高的营养价值,是一种很有前途的活体饲料。然而,它对盐度胁迫的反应仍然知之甚少。本研究采用多组学方法,整合转录组学、脂肪酸谱和微生物组分析,以评估低盐度(15 ppt)与对照组(25 ppt)的适应性。RNA-seq鉴定出6371个差异表达基因,包括294个富集于21个KEGG通路的免疫相关基因。上调的基因包括模式识别受体(PRRs)、丝氨酸蛋白酶、过氧化物酶和抗菌效应基因,而与氧化应激和蛋白酶抑制相关的基因则下调。此外,136个脂质代谢相关基因的差异表达表现为去饱和酶选择性上调,延长酶选择性下调。脂肪酸分析显示,各组间总多不饱和脂肪酸(PUFA)、二十二碳六烯酸(DHA)和二十碳五烯酸(EPA)含量无显著差异,但n-6 PUFA和花生四烯酸(ARA)含量在低盐度条件下显著升高。微生物组分析显示,低盐度组的细菌丰富度增加,群落组成发生变化,包括假单胞菌和绿原体的丰度升高,弧菌的水平降低。这些发现表明,盐度胁迫可调节a . royi-TH的免疫反应、脂质生物合成和微生物组成,从而深入了解其适应性代谢和免疫反应,以及其作为水产养殖中具有弹性和营养价值的活饲料的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-omics insights into the response of the tropical copepod Apocyclops royi-TH to salinity stress: implications for immunity and polyunsaturated fatty acid biosynthesis
Salinity is a key environmental factor influencing biological processes in aquatic organisms. Apocyclops royi-TH, a copepod species native to Thailand, is a promising live feed candidate due to its high nutritional value. However, its responses to salinity stress remain poorly understood. This study employed a multi-omics approach, integrating transcriptomics, fatty acid profiling, and microbiome analysis, to assess low-salinity (15 ppt) adaptation versus a control (25 ppt). RNA-seq identified 6371 differentially expressed genes, including 294 immune-related genes enriched in 21 KEGG pathways. Up-regulated genes included pattern recognition receptors (PRRs), serine proteases, peroxidases, and antimicrobial effectors, while genes related to oxidative stress and proteinase inhibition were down-regulated. Additionally, 136 genes related to lipid metabolism were differentially expressed, with selective up-regulation of desaturases and down-regulation of elongases. Fatty acid analysis showed no significant differences in total polyunsaturated fatty acid (PUFA), docosahexaenoic acid (DHA), or eicosapentaenoic acid (EPA) between groups, but levels of n-6 PUFA and arachidonic acid (ARA) were significantly higher under low salinity. Microbiome profiling revealed increased bacterial richness and a shifted community composition in the low salinity group, including elevated abundance of Pseudomonas and Acholeplasma, and reduced levels of Vibrio. These findings demonstrate that salinity stress modulates immune responses, lipid biosynthesis, and microbial composition in A. royi-TH, offering insights into its adaptive metabolic and immune responses, and its potential as a resilient and nutritionally valuable live feed in aquaculture.
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来源期刊
CiteScore
6.20
自引率
6.90%
发文量
206
审稿时长
49 days
期刊介绍: Developmental and Comparative Immunology (DCI) is an international journal that publishes articles describing original research in all areas of immunology, including comparative aspects of immunity and the evolution and development of the immune system. Manuscripts describing studies of immune systems in both vertebrates and invertebrates are welcome. All levels of immunological investigations are appropriate: organismal, cellular, biochemical and molecular genetics, extending to such fields as aging of the immune system, interaction between the immune and neuroendocrine system and intestinal immunity.
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