Integrated Vibrio load variation and transcriptome profiles provide new insights into the defensive response of Cyclina sinensis under Vibrio parahaemolyticus infection

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology D-Genomics & Proteomics Pub Date : 2025-06-01 Epub Date: 2025-02-01 DOI:10.1016/j.cbd.2025.101434
Fengjuan Jiang , Jiaxiao Sun , Kun Liu , Xin Li , Yanqing Shao , Qing Nie , Dehui Sun , Xiuke Ouyang , Weihong Zhao
{"title":"Integrated Vibrio load variation and transcriptome profiles provide new insights into the defensive response of Cyclina sinensis under Vibrio parahaemolyticus infection","authors":"Fengjuan Jiang ,&nbsp;Jiaxiao Sun ,&nbsp;Kun Liu ,&nbsp;Xin Li ,&nbsp;Yanqing Shao ,&nbsp;Qing Nie ,&nbsp;Dehui Sun ,&nbsp;Xiuke Ouyang ,&nbsp;Weihong Zhao","doi":"10.1016/j.cbd.2025.101434","DOIUrl":null,"url":null,"abstract":"<div><div><em>Vibrio parahaemolyticus</em> is the dominant pathogen in mariculture, leading to the bivalves' mass summer mortality. This study investigated the antibacterial defense mechanism of the <em>Cyclina sinensis against V. parahaemolyticus</em>. The immersion challenge revealed that the daily mortality of <em>C. sinensis</em> increased and then decreased gradually, and the mass mortality occurred about a week after <em>V. parahaemolyticus</em> infection. The <em>Vibrio</em> load in the hepatopancreas of <em>C. sinensis</em> was dramatically increased at 12–24 hpi (hours post-infection) and then declined significantly at 2–7 dpi (days post-infection). RNA-Seq generated 866 differentially expressed genes (DEGs), and KEGG analyses enriched multiple innate immune-related and metabolic-related pathways. The expression levels of nine immune-related and metabolic-related DEGs were significantly changed after <em>Vibrio</em> infection, and their temporal expression patterns were multiple. Our results indicated that the immunity and metabolic responses might be reprogrammed to protect the host against pathogens at the early infection phase. This study would expand our knowledge of the pathogenesis mechanisms of clams infected with <em>Vibrio</em> and provide a theoretical basis for healthy shellfish cultivation.</div></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":"54 ","pages":"Article 101434"},"PeriodicalIF":2.2000,"publicationDate":"2025-06-01","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/S1744117X2500022X","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/1 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Vibrio parahaemolyticus is the dominant pathogen in mariculture, leading to the bivalves' mass summer mortality. This study investigated the antibacterial defense mechanism of the Cyclina sinensis against V. parahaemolyticus. The immersion challenge revealed that the daily mortality of C. sinensis increased and then decreased gradually, and the mass mortality occurred about a week after V. parahaemolyticus infection. The Vibrio load in the hepatopancreas of C. sinensis was dramatically increased at 12–24 hpi (hours post-infection) and then declined significantly at 2–7 dpi (days post-infection). RNA-Seq generated 866 differentially expressed genes (DEGs), and KEGG analyses enriched multiple innate immune-related and metabolic-related pathways. The expression levels of nine immune-related and metabolic-related DEGs were significantly changed after Vibrio infection, and their temporal expression patterns were multiple. Our results indicated that the immunity and metabolic responses might be reprogrammed to protect the host against pathogens at the early infection phase. This study would expand our knowledge of the pathogenesis mechanisms of clams infected with Vibrio and provide a theoretical basis for healthy shellfish cultivation.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
综合弧菌负荷变化和转录组谱为中华环虫在副溶血性弧菌感染下的防御反应提供了新的见解
副溶血性弧菌是海水养殖的主要病原菌,是造成双壳类夏季大量死亡的主要原因。本研究探讨了中华环虫对副溶血性弧菌的抗菌防御机制。浸水攻毒法发现,中华按蚊日死亡率先升高后逐渐下降,在感染副溶血性弧菌后约1周左右出现大量死亡。在12-24 hpi(感染后h)时,中华按蚊肝胰腺弧菌载量显著增加,在2-7 dpi(感染后d)时显著下降。RNA-Seq产生了866个差异表达基因(deg), KEGG分析丰富了多种先天免疫相关和代谢相关的途径。感染弧菌后,9种免疫相关和代谢相关deg的表达水平发生显著变化,且时间表达模式多样。我们的研究结果表明,免疫和代谢反应可能被重新编程,以保护宿主在感染早期免受病原体的侵害。本研究将扩大我们对贝类感染弧菌发病机制的认识,并为贝类的健康养殖提供理论依据。
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 去求助
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.
期刊最新文献
Postbiotics from Saccharomyces cerevisiae fermentation protect the Chinese mitten crab (Eriocheir sinensis) against hypoxia-thermal stress through metabolic regulation and antioxidant defense Transcriptomic insights into the molecular basis of brachyurization of the mud crab Scylla paramamosain Integrative transcriptomic and metabolomic analysis of body color formation in transparent goldfish (Carassius auratus) Explosive expansion and functional specialization of SCP genes associated with “drifting” behavior in the hard clam Meretrix meretrix Molecular characterization of ionotropic receptors of a parasitic copepod Caligus fugu (Crustacea: Copepoda)
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1