Skin transcriptome of lenok trout (Brachymystax lenok) provides new insight on lectin genes and immune response mechanisms to Aeromonas salmonicida infection

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hui Liu, Maolin Wang, Jiayu Du, Shuai Wang, Zheng Zhang, Tingting He, Yuang Wang, Yan Chen, Wei Wang, Xuejie Li
{"title":"Skin transcriptome of lenok trout (Brachymystax lenok) provides new insight on lectin genes and immune response mechanisms to Aeromonas salmonicida infection","authors":"Hui Liu,&nbsp;Maolin Wang,&nbsp;Jiayu Du,&nbsp;Shuai Wang,&nbsp;Zheng Zhang,&nbsp;Tingting He,&nbsp;Yuang Wang,&nbsp;Yan Chen,&nbsp;Wei Wang,&nbsp;Xuejie Li","doi":"10.1016/j.cbd.2025.101439","DOIUrl":null,"url":null,"abstract":"<div><div><em>Brachymystax lenok</em> is an economically valuable cold-water fish species that has shown lower morbidity during pathogen outbreaks compared to other cold-water species. To elucidate the innate immune mechanisms in <em>B. lenok</em> in response to <em>Aeromonas salmonicida</em> infection, the transcriptome sequencing of the skin was performed. A total of 297,142 unigenes were generated, with 64.21 % (190,809) successfully annotated. Differential expression analysis identified 9238 differentially expressed genes (DEGs), with significant enrichment in immune-related pathways, including NOD-like receptor, C-type lectin receptor, and Toll-like receptor signalling pathways. These pathways may play crucial role in pathogen recognition, immune activation, inflammation, and the induction of adaptive immune responses in <em>B. lenok</em>. Further analysis revealed significant upregulation of pro-inflammatory cytokines, complement system components, and antimicrobial peptides such as hepcidin and cathelicidin, highlighting their pivotal roles in <em>B. lenok</em>'s immune defense. Moreover, a notable finding was the dynamic expression of various lectin families, including C-type lectins, plectins, galectin-3, and β-galactoside-binding lectins, which are involved in pathogen recognition, immune modulation, and cell signalling. Lectins may also contribute to resistance mechanisms by affecting bacterial membrane permeability, disrupting vital metabolic processes, and enhancing synergy with antimicrobial peptides. In the pathological experiments, histological examination correlated the upregulation of inflammatory mediators and complement components with tissue damage, immune cell infiltration, and lesion development, further supporting the involvement of these genes in the immune response. These results will enrich the information in understanding the immune response in <em>B. lenok</em>, and provide basic data for the following proteomics and functional assays that can verify the protein-level activity of these immune-related genes and clarify their specific roles in host defense and resistance mechanisms. This comprehensive transcriptome analysis provides insights into the immune response mechanisms of <em>B. lenok</em>, with particular emphasis on the role of lectins in pathogen recognition and resistance. These findings offer a foundation for further research on immune mechanisms in fish and the development of therapeutic strategies to mitigate infections in aquaculture.</div></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":"54 ","pages":"Article 101439"},"PeriodicalIF":2.2000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X25000279","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Brachymystax lenok is an economically valuable cold-water fish species that has shown lower morbidity during pathogen outbreaks compared to other cold-water species. To elucidate the innate immune mechanisms in B. lenok in response to Aeromonas salmonicida infection, the transcriptome sequencing of the skin was performed. A total of 297,142 unigenes were generated, with 64.21 % (190,809) successfully annotated. Differential expression analysis identified 9238 differentially expressed genes (DEGs), with significant enrichment in immune-related pathways, including NOD-like receptor, C-type lectin receptor, and Toll-like receptor signalling pathways. These pathways may play crucial role in pathogen recognition, immune activation, inflammation, and the induction of adaptive immune responses in B. lenok. Further analysis revealed significant upregulation of pro-inflammatory cytokines, complement system components, and antimicrobial peptides such as hepcidin and cathelicidin, highlighting their pivotal roles in B. lenok's immune defense. Moreover, a notable finding was the dynamic expression of various lectin families, including C-type lectins, plectins, galectin-3, and β-galactoside-binding lectins, which are involved in pathogen recognition, immune modulation, and cell signalling. Lectins may also contribute to resistance mechanisms by affecting bacterial membrane permeability, disrupting vital metabolic processes, and enhancing synergy with antimicrobial peptides. In the pathological experiments, histological examination correlated the upregulation of inflammatory mediators and complement components with tissue damage, immune cell infiltration, and lesion development, further supporting the involvement of these genes in the immune response. These results will enrich the information in understanding the immune response in B. lenok, and provide basic data for the following proteomics and functional assays that can verify the protein-level activity of these immune-related genes and clarify their specific roles in host defense and resistance mechanisms. This comprehensive transcriptome analysis provides insights into the immune response mechanisms of B. lenok, with particular emphasis on the role of lectins in pathogen recognition and resistance. These findings offer a foundation for further research on immune mechanisms in fish and the development of therapeutic strategies to mitigate infections in aquaculture.
褐鳟(Brachymystax lenok)的皮肤转录组为凝集素基因和沙门氏菌气单胞菌感染的免疫反应机制提供了新的见解
短mystax lenok是一种具有经济价值的冷水鱼类,与其他冷水鱼类相比,在病原体爆发期间发病率较低。为了阐明B. lenok对沙门氏菌气单胞菌感染的先天免疫机制,对皮肤进行了转录组测序。共生成297,142个unigenes,成功注释64.21%(190,809)。差异表达分析鉴定出9238个差异表达基因(DEGs),在免疫相关途径中显著富集,包括nod样受体、c型凝集素受体和toll样受体信号通路。这些途径可能在芽孢杆菌的病原体识别、免疫激活、炎症和诱导适应性免疫反应中发挥重要作用。进一步分析发现,促炎细胞因子、补体系统成分和抗菌肽(如hepcidin和cathelicidin)显著上调,突出了它们在B. lenok免疫防御中的关键作用。此外,一个值得注意的发现是各种凝集素家族的动态表达,包括c型凝集素、凝集素、半乳糖素-3和β-半乳糖苷结合凝集素,它们参与病原体识别、免疫调节和细胞信号传导。凝集素也可能通过影响细菌膜的通透性、破坏重要的代谢过程和增强与抗菌肽的协同作用来促进耐药性机制。在病理实验中,组织学检查将炎症介质和补体成分的上调与组织损伤、免疫细胞浸润和病变发展联系起来,进一步支持这些基因参与免疫反应。这些结果将丰富了解B. lenok免疫应答的信息,并为后续的蛋白质组学和功能分析提供基础数据,以验证这些免疫相关基因的蛋白水平活性,阐明其在宿主防御和抗性机制中的具体作用。这项全面的转录组分析提供了对B. lenok免疫应答机制的深入了解,特别强调了凝集素在病原体识别和抗性中的作用。这些发现为进一步研究鱼类免疫机制和开发减轻水产养殖感染的治疗策略奠定了基础。
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
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.
×
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