Transcriptomic analysis of immune and metabolic responses in largemouth bass (Micropterus salmoides) challenged with Citrobacter freundii.

IF 2 3区 农林科学 Q2 FISHERIES
Xiao He, Zheling Zhang, Yanbing Zhang, Wei Sun, Chi Zhang, Xiaodan Liu
{"title":"Transcriptomic analysis of immune and metabolic responses in largemouth bass (Micropterus salmoides) challenged with Citrobacter freundii.","authors":"Xiao He, Zheling Zhang, Yanbing Zhang, Wei Sun, Chi Zhang, Xiaodan Liu","doi":"10.1111/jfb.70193","DOIUrl":null,"url":null,"abstract":"<p><p>Citrobacter freundii, a common zoonotic pathogen affecting humans, livestock and fish, is recognized for its substantial impact on largemouth bass (Micropterus salmoides) mortality. However, the mechanisms of C. freundii infection in largemouth bass remain poorly understood. Based on the results of extracellular enzyme activity detection, it was speculated that the production of extracellular enzymes may be related to bacterial pathogenicity. To elucidate the immune response mechanism, transcriptomic analysis was conducted on spleen tissues from largemouth bass infected with C. freundii. Following quality filtering, the control group generated 44.04 million clean reads, while the infected group produced 44.32 million clean reads. A total of 385 differentially expressed genes (DEGs) were identified, comprising 224 up-regulated and 161 down-regulated unigenes. Classification using the Gene Ontology and Kyoto Encyclopedia of Genes and Genomes databases further elucidated the biological functions and signalling pathways of the DEGs. Significantly impacted pathways included 'Galactose metabolism', ' Pyrimidine metabolism', ' Alanine, aspartate and glutamate metabolism', 'Ubiquitin-mediated proteolysis', 'Endocytosis', 'Phagosome' and 'SNARE interactions in vesicular transport', underscoring their roles in metabolic and immune-related signalling. Eight DEGs were chosen and validated for their expression levels via real-time quantitative PCR. This study offered molecular insights into the host defence mechanisms against C. freundii infection, contributing to the formulation of disease prevention and control strategies for largemouth bass aquaculture.</p>","PeriodicalId":15794,"journal":{"name":"Journal of fish biology","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of fish biology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/jfb.70193","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

Abstract

Citrobacter freundii, a common zoonotic pathogen affecting humans, livestock and fish, is recognized for its substantial impact on largemouth bass (Micropterus salmoides) mortality. However, the mechanisms of C. freundii infection in largemouth bass remain poorly understood. Based on the results of extracellular enzyme activity detection, it was speculated that the production of extracellular enzymes may be related to bacterial pathogenicity. To elucidate the immune response mechanism, transcriptomic analysis was conducted on spleen tissues from largemouth bass infected with C. freundii. Following quality filtering, the control group generated 44.04 million clean reads, while the infected group produced 44.32 million clean reads. A total of 385 differentially expressed genes (DEGs) were identified, comprising 224 up-regulated and 161 down-regulated unigenes. Classification using the Gene Ontology and Kyoto Encyclopedia of Genes and Genomes databases further elucidated the biological functions and signalling pathways of the DEGs. Significantly impacted pathways included 'Galactose metabolism', ' Pyrimidine metabolism', ' Alanine, aspartate and glutamate metabolism', 'Ubiquitin-mediated proteolysis', 'Endocytosis', 'Phagosome' and 'SNARE interactions in vesicular transport', underscoring their roles in metabolic and immune-related signalling. Eight DEGs were chosen and validated for their expression levels via real-time quantitative PCR. This study offered molecular insights into the host defence mechanisms against C. freundii infection, contributing to the formulation of disease prevention and control strategies for largemouth bass aquaculture.

弗氏柠檬酸杆菌对大口黑鲈免疫和代谢反应的转录组学分析。
弗氏柠檬酸杆菌是一种影响人类、牲畜和鱼类的常见人畜共患病原体,因其对大口黑鲈(Micropterus salmoides)死亡率的重大影响而得到公认。然而,弗氏弓形虫感染大口黑鲈的机制仍然知之甚少。根据胞外酶活性检测结果,推测胞外酶的产生可能与细菌致病性有关。为了阐明免疫应答机制,我们对感染弗氏梭菌的大口黑鲈脾脏组织进行了转录组学分析。经过质量过滤,对照组产生了4404万次干净读取,而感染组产生了4432万次干净读取。共鉴定出385个差异表达基因(deg),其中上调224个,下调161个。利用基因本体和京都基因与基因组百科数据库的分类进一步阐明了deg的生物学功能和信号通路。受到显著影响的途径包括“半乳糖代谢”、“嘧啶代谢”、“丙氨酸、天冬氨酸和谷氨酸代谢”、“泛素介导的蛋白质水解”、“内吞作用”、“吞噬体”和“囊泡运输中的SNARE相互作用”,强调了它们在代谢和免疫相关信号传导中的作用。选择8个deg并通过实时定量PCR验证其表达水平。本研究为了解宿主对弗氏弓形虫感染的防御机制提供了分子视角,有助于制定大口黑鲈养殖疾病预防和控制策略。
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
Journal of fish biology
Journal of fish biology 生物-海洋与淡水生物学
CiteScore
4.00
自引率
10.00%
发文量
292
审稿时长
3 months
期刊介绍: The Journal of Fish Biology is a leading international journal for scientists engaged in all aspects of fishes and fisheries research, both fresh water and marine. The journal publishes high-quality papers relevant to the central theme of fish biology and aims to bring together under one cover an overall picture of the research in progress and to provide international communication among researchers in many disciplines with a common interest in the biology of fish.
×
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