Oral administration of LEAP2 enhances immunity against Edwardsiella tarda through regulation of gut bacterial community and metabolite in mudskipper

IF 4.1 2区 农林科学 Q1 FISHERIES Fish & shellfish immunology Pub Date : 2025-01-15 DOI:10.1016/j.fsi.2025.110128
Ting-Fang Zhu , Hai-Peng Guo , Li Nie , Jiong Chen
{"title":"Oral administration of LEAP2 enhances immunity against Edwardsiella tarda through regulation of gut bacterial community and metabolite in mudskipper","authors":"Ting-Fang Zhu ,&nbsp;Hai-Peng Guo ,&nbsp;Li Nie ,&nbsp;Jiong Chen","doi":"10.1016/j.fsi.2025.110128","DOIUrl":null,"url":null,"abstract":"<div><div>The liver-expressed antimicrobial peptide 2 (LEAP2) is gaining recognition for its immune regulatory functions beyond direct antimicrobial activity. In this study, we investigated the role of mudskipper (<em>Boleophthalmus pectinirostris</em>) LEAP2 (<em>Bp</em>LEAP2) in enhancing the survival, gut health, and immune resilience against <em>Edwardsiella tarda</em> infection. Pre-oral delivery of <em>Bp</em>LEAP2 significantly improved survival rates and mitigated infection-induced damage to the gut, as evidenced by preserved villus length and goblet cell count. Analysis of gut microbial communities using 16S rRNA sequencing revealed that pre-oral delivery of <em>Bp</em>LEAP2 increased microbial diversity, evenness, and the abundance of beneficial genera such as <em>Pseudoalteromonas</em> and <em>Shewanella</em>, while reducing pathogenic genera like <em>Pseudorhodobacter</em>. Metabolomic profiling showed that <em>Bp</em>LEAP2 altered the gut metabolite composition, significantly increasing levels of bile acids and amino acids, which are known to support gut health and immune responses. Correlation analysis demonstrated strong positive associations between <em>Bp</em>LEAP2-induced microbial shifts and increased metabolites involved in amino acid metabolism. These findings suggest that <em>Bp</em>LEAP2 promotes intestinal homeostasis by modulating gut microbiota composition and enhancing beneficial metabolite production, ultimately improving gut barrier integrity and conferring resistance against <em>E. tarda</em> infection. This study highlights the potential application of <em>Bp</em>LEAP2 in enhancing disease resilience in aquaculture species, offering a promising strategy for sustainable aquaculture practices.</div></div>","PeriodicalId":12127,"journal":{"name":"Fish & shellfish immunology","volume":"158 ","pages":"Article 110128"},"PeriodicalIF":4.1000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fish & shellfish immunology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1050464825000178","RegionNum":2,"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

The liver-expressed antimicrobial peptide 2 (LEAP2) is gaining recognition for its immune regulatory functions beyond direct antimicrobial activity. In this study, we investigated the role of mudskipper (Boleophthalmus pectinirostris) LEAP2 (BpLEAP2) in enhancing the survival, gut health, and immune resilience against Edwardsiella tarda infection. Pre-oral delivery of BpLEAP2 significantly improved survival rates and mitigated infection-induced damage to the gut, as evidenced by preserved villus length and goblet cell count. Analysis of gut microbial communities using 16S rRNA sequencing revealed that pre-oral delivery of BpLEAP2 increased microbial diversity, evenness, and the abundance of beneficial genera such as Pseudoalteromonas and Shewanella, while reducing pathogenic genera like Pseudorhodobacter. Metabolomic profiling showed that BpLEAP2 altered the gut metabolite composition, significantly increasing levels of bile acids and amino acids, which are known to support gut health and immune responses. Correlation analysis demonstrated strong positive associations between BpLEAP2-induced microbial shifts and increased metabolites involved in amino acid metabolism. These findings suggest that BpLEAP2 promotes intestinal homeostasis by modulating gut microbiota composition and enhancing beneficial metabolite production, ultimately improving gut barrier integrity and conferring resistance against E. tarda infection. This study highlights the potential application of BpLEAP2 in enhancing disease resilience in aquaculture species, offering a promising strategy for sustainable aquaculture practices.
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
口服LEAP2通过调节弹涂鱼肠道细菌群落和代谢物来增强对迟发爱德华氏菌的免疫。
肝脏表达的抗菌肽2 (LEAP2)因其超越直接抗菌活性的免疫调节功能而获得认可。在这项研究中,我们研究了弹涂鱼(Boleophthalmus pectinrostris) LEAP2 (BpLEAP2)在提高存活、肠道健康和免疫恢复能力方面对迟达爱德华菌感染的作用。通过保留绒毛长度和杯状细胞计数可以证明,口服前给药BpLEAP2显著提高了存活率,减轻了感染引起的肠道损伤。利用16S rRNA测序对肠道微生物群落进行分析发现,口服前给药BpLEAP2增加了微生物多样性、均匀性和有益菌(如假异单胞菌和希瓦氏菌)的丰度,同时减少了致病性菌(如假弓形杆菌)的数量。代谢组学分析显示,BpLEAP2改变了肠道代谢物的组成,显著增加了胆汁酸和氨基酸的水平,而胆汁酸和氨基酸是支持肠道健康和免疫反应的物质。相关分析表明,bpleap2诱导的微生物转移与氨基酸代谢相关的代谢物增加之间存在很强的正相关。这些研究结果表明,BpLEAP2通过调节肠道菌群组成和提高有益代谢物的产生来促进肠道稳态,最终改善肠道屏障的完整性并赋予对迟达杆菌感染的抵抗力。本研究强调了BpLEAP2在提高水产养殖物种抗病性方面的潜在应用,为可持续水产养殖实践提供了有前途的策略。
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 去求助
来源期刊
Fish & shellfish immunology
Fish & shellfish immunology 农林科学-海洋与淡水生物学
CiteScore
7.50
自引率
19.10%
发文量
750
审稿时长
68 days
期刊介绍: Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.
期刊最新文献
Contribution of interleukins in the regulation of teleost fish immunity: A review from the perspective of regulating macrophages. Functional study of tilapia T cell activation stimulus signal molecule CD2. NF-κB inhibitor PDTC involved in regulating the transplantation immunity in the pearl oyster Pinctada fucata martensii. The accessory secretion system in Streptococcus agalactiae regulates protein secretion, stress resistance, adhesion, immune evasion, and virulence. Gut microbiota and functional metabolic predictions in white feces disease-infected Pacific white shrimp, Penaeus vannamei, from Indonesian farms
×
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学术文献互助
Book学术文献互助群
群 号:481959085
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