Acquired immunity mechanisms in sheep infected with Nematodirus oiratianus: key genes and host responses.

IF 2.9 2区 农林科学 Q1 VETERINARY SCIENCES
Frontiers in Veterinary Science Pub Date : 2025-09-04 eCollection Date: 2025-01-01 DOI:10.3389/fvets.2025.1643786
Bin Hou, Rina Su, Dalai Suyala, Li Xu, Ruiyuan Zhao, Puguo Hao, Yali Wang, Fei Mao, Bo Wu, Xuedong Ding, Runqing Han, Xuesong Peng, Risu Na, Yihong Hao, Qimuge Bainuwen, Xiaojia Mu, Surong Hasi
{"title":"Acquired immunity mechanisms in sheep infected with <i>Nematodirus oiratianus</i>: key genes and host responses.","authors":"Bin Hou, Rina Su, Dalai Suyala, Li Xu, Ruiyuan Zhao, Puguo Hao, Yali Wang, Fei Mao, Bo Wu, Xuedong Ding, Runqing Han, Xuesong Peng, Risu Na, Yihong Hao, Qimuge Bainuwen, Xiaojia Mu, Surong Hasi","doi":"10.3389/fvets.2025.1643786","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Controlling gastrointestinal nematode infections poses a major challenge in intensive farming, worsened by rising anthelmintic resistance. Developing innovative control strategies is critical. Sheep acquired immunity to <i>Nematodirus oiratianus</i> offers a valuable model for dissecting host-nematode interactions, though underlying immune mechanisms remain unclear.</p><p><strong>Methods: </strong>This study employed multi-omics analyses (transcriptome and proteome) of lamb duodenum across infection stages, validated by RT-qPCR, iELISA, histopathological staining (HE), and electron microscopy.</p><p><strong>Results and conclusions: </strong>Infection triggered early immune activation mediated by intestinal epithelial cells. Key differentially expressed genes included <i>CLDN18</i>, <i>CCL19</i>, <i>FGB</i>, and <i>Muc5ac</i>, potentially linking to parasite expulsion. Early-stage pathway enrichment in cancer, chemokine signaling, and phagosome function enhanced intestinal barrier integrity and immune cell recruitment. Late-stage upregulation of <i>CCL</i> chemokines directly impacted nematode survival. Intestinal villi shedding was also correlated with parasite clearance. These findings unravel potential mechanisms of acquired immunity against <i>Nematodirus oiratianus</i>, highlighting novel therapeutic targets (e.g., epithelial barrier regulators, chemokine networks) and vaccine candidates for nematode control in livestock.</p>","PeriodicalId":12772,"journal":{"name":"Frontiers in Veterinary Science","volume":"12 ","pages":"1643786"},"PeriodicalIF":2.9000,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445057/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Veterinary Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.3389/fvets.2025.1643786","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Controlling gastrointestinal nematode infections poses a major challenge in intensive farming, worsened by rising anthelmintic resistance. Developing innovative control strategies is critical. Sheep acquired immunity to Nematodirus oiratianus offers a valuable model for dissecting host-nematode interactions, though underlying immune mechanisms remain unclear.

Methods: This study employed multi-omics analyses (transcriptome and proteome) of lamb duodenum across infection stages, validated by RT-qPCR, iELISA, histopathological staining (HE), and electron microscopy.

Results and conclusions: Infection triggered early immune activation mediated by intestinal epithelial cells. Key differentially expressed genes included CLDN18, CCL19, FGB, and Muc5ac, potentially linking to parasite expulsion. Early-stage pathway enrichment in cancer, chemokine signaling, and phagosome function enhanced intestinal barrier integrity and immune cell recruitment. Late-stage upregulation of CCL chemokines directly impacted nematode survival. Intestinal villi shedding was also correlated with parasite clearance. These findings unravel potential mechanisms of acquired immunity against Nematodirus oiratianus, highlighting novel therapeutic targets (e.g., epithelial barrier regulators, chemokine networks) and vaccine candidates for nematode control in livestock.

Abstract Image

Abstract Image

Abstract Image

绵羊感染伊氏线虫的获得性免疫机制:关键基因和宿主反应。
背景:控制胃肠道线虫感染是集约化农业面临的主要挑战,并且随着抗虫性的上升而恶化。制定创新的控制战略至关重要。绵羊对伊氏线虫的获得性免疫为解剖宿主-线虫相互作用提供了一个有价值的模型,尽管潜在的免疫机制尚不清楚。方法:本研究采用多组学方法(转录组和蛋白质组)分析了羔羊十二指肠不同感染阶段的转录组和蛋白质组,并通过RT-qPCR、iELISA、组织病理学染色(HE)和电镜进行了验证。结果与结论:感染触发肠上皮细胞介导的早期免疫激活。关键的差异表达基因包括CLDN18、CCL19、FGB和Muc5ac,可能与寄生虫驱逐有关。癌症、趋化因子信号和吞噬体功能的早期通路富集增强了肠屏障的完整性和免疫细胞的募集。晚期CCL趋化因子的上调直接影响线虫的存活。肠绒毛脱落也与寄生虫清除有关。这些发现揭示了获得性免疫对抗伊氏线虫的潜在机制,强调了新的治疗靶点(如上皮屏障调节剂、趋化因子网络)和家畜线虫控制的候选疫苗。
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
Frontiers in Veterinary Science
Frontiers in Veterinary Science Veterinary-General Veterinary
CiteScore
4.80
自引率
9.40%
发文量
1870
审稿时长
14 weeks
期刊介绍: Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy. Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field. Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.
×
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