Adaptation responses to salt stress in the gut of Poecilia reticulata.

IF 2.5 2区 生物学 Q3 CELL BIOLOGY
Animal Cells and Systems Pub Date : 2025-01-18 eCollection Date: 2025-01-01 DOI:10.1080/19768354.2025.2451413
Hyerim Lee, Hyunjae Yeo, Jihye Park, Keunsoo Kang, Sun-Ju Yi, Kyunghwan Kim
{"title":"Adaptation responses to salt stress in the gut of <i>Poecilia reticulata</i>.","authors":"Hyerim Lee, Hyunjae Yeo, Jihye Park, Keunsoo Kang, Sun-Ju Yi, Kyunghwan Kim","doi":"10.1080/19768354.2025.2451413","DOIUrl":null,"url":null,"abstract":"<p><p>Osmoregulation is essential for the survival of aquatic organisms, particularly teleost fish facing osmotic challenges in environments characterized by variable salinity. While the gills are known for ion exchange, the intestine's role in water and salt absorption is gaining attention. Here, we investigated the adaptive responses of the intestine to salinity stress in guppies (<i>Poecilia reticulata</i>), observing significant morphological and transcriptomic alterations. Guppies showed superior salt tolerance compared to zebrafish (<i>Danio rerio</i>). Increasing salinity reduced villus length and intestinal diameter in guppies, while zebrafish exhibited damage to villus structure and loss of goblet cells. Transcriptomic analysis identified key genes involved in osmoregulation, tissue remodeling, and immune modulation. Upregulated genes included the solute carrier transporters <i>slc2al</i> and <i>slc3al</i>, which facilitate ion and water transport, as well as a transcription factor AP-1 subunit and phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta, both of which participate in tissue repair and growth responses. In contrast, many genes related to the innate immune system (such as <i>Tnfaip6</i>) were downregulated, suggesting a shift toward the prioritization of osmoregulatory functions over immune responses. Interestingly, the differential expression of adaptation genes was linked to variations in epigenetic modifications and transcription factor activity. Transcription factors crucial for adapting to salt stress, such as <i>bhlhe40</i>, <i>cebpd</i>, and <i>gata6,</i> were progressively upregulated in guppies but remained downregulated in zebrafish. Our findings highlight the intricate mechanisms of adaptation to salinity stress in <i>P. reticulata</i>, providing insights into osmoregulatory mechanisms involving the intestine in aquatic organisms.</p>","PeriodicalId":7804,"journal":{"name":"Animal Cells and Systems","volume":"29 1","pages":"84-99"},"PeriodicalIF":2.5000,"publicationDate":"2025-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11749108/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Cells and Systems","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/19768354.2025.2451413","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Osmoregulation is essential for the survival of aquatic organisms, particularly teleost fish facing osmotic challenges in environments characterized by variable salinity. While the gills are known for ion exchange, the intestine's role in water and salt absorption is gaining attention. Here, we investigated the adaptive responses of the intestine to salinity stress in guppies (Poecilia reticulata), observing significant morphological and transcriptomic alterations. Guppies showed superior salt tolerance compared to zebrafish (Danio rerio). Increasing salinity reduced villus length and intestinal diameter in guppies, while zebrafish exhibited damage to villus structure and loss of goblet cells. Transcriptomic analysis identified key genes involved in osmoregulation, tissue remodeling, and immune modulation. Upregulated genes included the solute carrier transporters slc2al and slc3al, which facilitate ion and water transport, as well as a transcription factor AP-1 subunit and phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta, both of which participate in tissue repair and growth responses. In contrast, many genes related to the innate immune system (such as Tnfaip6) were downregulated, suggesting a shift toward the prioritization of osmoregulatory functions over immune responses. Interestingly, the differential expression of adaptation genes was linked to variations in epigenetic modifications and transcription factor activity. Transcription factors crucial for adapting to salt stress, such as bhlhe40, cebpd, and gata6, were progressively upregulated in guppies but remained downregulated in zebrafish. Our findings highlight the intricate mechanisms of adaptation to salinity stress in P. reticulata, providing insights into osmoregulatory mechanisms involving the intestine in aquatic organisms.

网状水蛭肠道对盐胁迫的适应反应。
渗透调节对水生生物的生存至关重要,特别是硬骨鱼在盐度变化的环境中面临渗透挑战。虽然鳃以离子交换而闻名,但肠道在吸收水和盐方面的作用正在引起人们的关注。在这里,我们研究了孔雀鱼(Poecilia reticulata)肠道对盐度胁迫的适应性反应,观察到显著的形态和转录组变化。与斑马鱼(Danio rerio)相比,孔雀鱼具有更好的耐盐性。盐度增加使孔雀鱼的绒毛长度和肠直径减少,斑马鱼的绒毛结构受损,杯状细胞减少。转录组学分析确定了参与渗透调节、组织重塑和免疫调节的关键基因。上调的基因包括促进离子和水运输的溶质载体转运体slc2al和slc3al,以及转录因子AP-1亚基和磷脂酰肌醇-4,5-二磷酸3激酶催化亚基β,它们都参与组织修复和生长反应。相反,许多与先天免疫系统相关的基因(如Tnfaip6)被下调,表明渗透调节功能优先于免疫应答的转变。有趣的是,适应基因的差异表达与表观遗传修饰和转录因子活性的变化有关。对适应盐胁迫至关重要的转录因子,如bhlhe40、cebpd和gata6,在孔雀鱼中逐渐上调,但在斑马鱼中保持下调。我们的研究结果强调了网纹水螅适应盐度胁迫的复杂机制,为水生生物肠道渗透调节机制提供了见解。
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
Animal Cells and Systems
Animal Cells and Systems 生物-动物学
CiteScore
4.50
自引率
24.10%
发文量
33
审稿时长
6 months
期刊介绍: Animal Cells and Systems is the official journal of the Korean Society for Integrative Biology. This international, peer-reviewed journal publishes original papers that cover diverse aspects of biological sciences including Bioinformatics and Systems Biology, Developmental Biology, Evolution and Systematic Biology, Population Biology, & Animal Behaviour, Molecular and Cellular Biology, Neurobiology and Immunology, and Translational Medicine.
×
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:481959085
Book学术官方微信