Transcriptomic and BSA analysis provide insight into the metabolic regulation mechanism in filefish Thamnaconus septentrionalis under low salt stress

IF 3.9 1区 农林科学 Q1 FISHERIES
Jiang Wang , Wenhao Ren , Chunyan Zhao , Li Bian , Xianliang Meng , Yichao Ren , Aihuan Song
{"title":"Transcriptomic and BSA analysis provide insight into the metabolic regulation mechanism in filefish Thamnaconus septentrionalis under low salt stress","authors":"Jiang Wang ,&nbsp;Wenhao Ren ,&nbsp;Chunyan Zhao ,&nbsp;Li Bian ,&nbsp;Xianliang Meng ,&nbsp;Yichao Ren ,&nbsp;Aihuan Song","doi":"10.1016/j.aquaculture.2025.742792","DOIUrl":null,"url":null,"abstract":"<div><div>This study provided insights into the adaption of greenfin horse-faced filefish <em>Thamnaconus septentrionalis</em> toward low-salinity conditions. A combination of antioxidant enzyme activity, transcriptome technology, and BSA sequencing analysis was employed to investigate the osmotic balance, oxidative stress, and immune response in this species. The salinity levels were controlled at 21 PSU (control group), with two treatment groups, Group C (salinity reduction at a rate of 1 PSU per day) and Group A (salinity reduction at a rate of 6 PSU per day), respectively. As a result, with the decrease of salinity, the activities of SOD, CAT, and GSH-PX, as well as the content of MDA, showed varying degrees of increased. The findings indicated that a reduction in salinity can lead to oxidative damage induced by reactive oxygen species (ROS), which in turn activated the activity of antioxidant enzymes in fish to maintain the balance of ROS metabolism. When the salinity was reduced to 15 PSU, there were more DEGs in Groups A and Group C. The KEGG enrichment pathway showed that DEGs were most significantly enriched in the arachidonic acid metabolism, IL-17 signaling, glycine, serine, threonine metabolism, and glutathione metabolism pathways. The BSA sequencing results showed that single nucleotide polymorphisms (SNP) and insertions and deletions (Indel) were co-located on LG08, LG09, LG14, LG15, and LG19 chromosomes. A combined analysis revealed the identification of 52 SNP loci and 22 candidate genes on chromosomes associated with low-salt tolerance trait, which were significantly enriched in tight cell junctions, cytokine receptor interaction pathways, and signal transduction pathways. Upon conducting a joint analysis with the transcriptome, there were five genes, namely <em>CLDN20</em>, <em>IFI44L</em>, <em>MISP</em>, <em>TRIM25</em>, and <em>TSPAN33</em>, that demonstrated significant expression within the transcriptome-filtered DEGs. This study contributes significantly to advancing the understanding of osmotic regulation and immune response mechanism in <em>T. septentrionalis</em>.</div></div>","PeriodicalId":8375,"journal":{"name":"Aquaculture","volume":"609 ","pages":"Article 742792"},"PeriodicalIF":3.9000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquaculture","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0044848625006787","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

Abstract

This study provided insights into the adaption of greenfin horse-faced filefish Thamnaconus septentrionalis toward low-salinity conditions. A combination of antioxidant enzyme activity, transcriptome technology, and BSA sequencing analysis was employed to investigate the osmotic balance, oxidative stress, and immune response in this species. The salinity levels were controlled at 21 PSU (control group), with two treatment groups, Group C (salinity reduction at a rate of 1 PSU per day) and Group A (salinity reduction at a rate of 6 PSU per day), respectively. As a result, with the decrease of salinity, the activities of SOD, CAT, and GSH-PX, as well as the content of MDA, showed varying degrees of increased. The findings indicated that a reduction in salinity can lead to oxidative damage induced by reactive oxygen species (ROS), which in turn activated the activity of antioxidant enzymes in fish to maintain the balance of ROS metabolism. When the salinity was reduced to 15 PSU, there were more DEGs in Groups A and Group C. The KEGG enrichment pathway showed that DEGs were most significantly enriched in the arachidonic acid metabolism, IL-17 signaling, glycine, serine, threonine metabolism, and glutathione metabolism pathways. The BSA sequencing results showed that single nucleotide polymorphisms (SNP) and insertions and deletions (Indel) were co-located on LG08, LG09, LG14, LG15, and LG19 chromosomes. A combined analysis revealed the identification of 52 SNP loci and 22 candidate genes on chromosomes associated with low-salt tolerance trait, which were significantly enriched in tight cell junctions, cytokine receptor interaction pathways, and signal transduction pathways. Upon conducting a joint analysis with the transcriptome, there were five genes, namely CLDN20, IFI44L, MISP, TRIM25, and TSPAN33, that demonstrated significant expression within the transcriptome-filtered DEGs. This study contributes significantly to advancing the understanding of osmotic regulation and immune response mechanism in T. septentrionalis.
转录组学和牛血清蛋白分析有助于深入了解低盐胁迫下七片麻鱼的代谢调控机制
该研究为绿鳍马面鱼Thamnaconus septentrionalis对低盐度环境的适应提供了见解。采用抗氧化酶活性、转录组技术和BSA测序分析相结合的方法研究了该物种的渗透平衡、氧化应激和免疫反应。盐度水平控制在21 PSU(对照组),分为两个治疗组,C组(以每天1 PSU的速率降低盐度)和a组(以每天6 PSU的速率降低盐度)。结果表明,随着盐度的降低,SOD、CAT、GSH-PX活性以及MDA含量均有不同程度的升高。研究结果表明,盐度降低可导致活性氧(ROS)引起的氧化损伤,进而激活鱼类体内抗氧化酶的活性,维持ROS代谢的平衡。当盐度降至15 PSU时,A组和c组的deg数量增加。KEGG富集途径显示,deg在花生四烯酸代谢、IL-17信号通路、甘氨酸、丝氨酸、苏氨酸代谢和谷胱甘肽代谢通路中富集最为显著。BSA测序结果显示,单核苷酸多态性(SNP)和插入缺失(Indel)共存于LG08、LG09、LG14、LG15和LG19染色体上。综合分析发现,与低盐耐受性性状相关的染色体上共鉴定出52个SNP位点和22个候选基因,在细胞紧密连接、细胞因子受体相互作用通路和信号转导通路中显著富集。通过与转录组的联合分析,有5个基因CLDN20、IFI44L、MISP、TRIM25和TSPAN33在转录组过滤的deg中显著表达。本研究对深入了解七毛弓形虫的渗透调控和免疫应答机制具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Aquaculture
Aquaculture 农林科学-海洋与淡水生物学
CiteScore
8.60
自引率
17.80%
发文量
1246
审稿时长
56 days
期刊介绍: Aquaculture is an international journal for the exploration, improvement and management of all freshwater and marine food resources. It publishes novel and innovative research of world-wide interest on farming of aquatic organisms, which includes finfish, mollusks, crustaceans and aquatic plants for human consumption. Research on ornamentals is not a focus of the Journal. Aquaculture only publishes papers with a clear relevance to improving aquaculture practices or a potential application.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信