用编码衣壳蛋白和IFN-γ的DNA疫苗进行口服免疫,可激发对神经坏死病毒的有效和长期免疫。

IF 3.9 2区 农林科学 Q1 FISHERIES
Fish & shellfish immunology Pub Date : 2025-11-01 Epub Date: 2025-08-06 DOI:10.1016/j.fsi.2025.110641
Haihua Peng, Chen Zhang, Chunze Shang, Caoying Wei, Ying Wu, Zhenjie Cao, Pengfei Li, Yongcan Zhou, Yun Sun
{"title":"用编码衣壳蛋白和IFN-γ的DNA疫苗进行口服免疫,可激发对神经坏死病毒的有效和长期免疫。","authors":"Haihua Peng, Chen Zhang, Chunze Shang, Caoying Wei, Ying Wu, Zhenjie Cao, Pengfei Li, Yongcan Zhou, Yun Sun","doi":"10.1016/j.fsi.2025.110641","DOIUrl":null,"url":null,"abstract":"<p><p>Viral nervous necrosis (VNN), caused by nervous necrosis virus (NNV), poses a major threat to global aquaculture, causing severe mortality and economic losses in high-value species like grouper. Oral vaccination offers a practical approach for large-scale prevention but faces challenges including gastrointestinal antigen degradation and inadequate mucosal immunity. To overcome these, we developed an oral DNA vaccine by encapsulating a plasmid encoding the NNV capsid protein (CP) and IFN-γ within PLGA microparticles (CPIF@PLGA). Synthesized via double emulsion-solvent evaporation, these spherical microparticles (ca. 8 μm in diameter) exhibited high encapsulation efficiency (84.3 %). In vivo immunization of grouper demonstrated that CPIF@PLGA significantly increased survival to 82.2 % post-NNV challenge versus controls, reduced viral loads in brain and eyes, and enhanced systemic and mucosal immunity. This was evidenced by elevated serum IgM, IgT, lysozyme, SOD, and complement activity, alongside upregulated expression of immune-related genes (IL-1β, TNF-α, CD4, CD8α, MHC-Iα, IgM) in spleen and hindgut. Our findings establish PLGA microparticles as an effective oral delivery platform and IFN-γ as a potent adjuvant, eliciting robust and durable protection. This study provides a promising strategy for developing effective and scalable oral vaccines against NNV in aquaculture.</p>","PeriodicalId":12127,"journal":{"name":"Fish & shellfish immunology","volume":" ","pages":"110641"},"PeriodicalIF":3.9000,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oral immunization with a DNA vaccine encoding capsid protein and IFN-γ provokes efficient and long-term immunity against nervous necrosis virus.\",\"authors\":\"Haihua Peng, Chen Zhang, Chunze Shang, Caoying Wei, Ying Wu, Zhenjie Cao, Pengfei Li, Yongcan Zhou, Yun Sun\",\"doi\":\"10.1016/j.fsi.2025.110641\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Viral nervous necrosis (VNN), caused by nervous necrosis virus (NNV), poses a major threat to global aquaculture, causing severe mortality and economic losses in high-value species like grouper. Oral vaccination offers a practical approach for large-scale prevention but faces challenges including gastrointestinal antigen degradation and inadequate mucosal immunity. To overcome these, we developed an oral DNA vaccine by encapsulating a plasmid encoding the NNV capsid protein (CP) and IFN-γ within PLGA microparticles (CPIF@PLGA). Synthesized via double emulsion-solvent evaporation, these spherical microparticles (ca. 8 μm in diameter) exhibited high encapsulation efficiency (84.3 %). In vivo immunization of grouper demonstrated that CPIF@PLGA significantly increased survival to 82.2 % post-NNV challenge versus controls, reduced viral loads in brain and eyes, and enhanced systemic and mucosal immunity. This was evidenced by elevated serum IgM, IgT, lysozyme, SOD, and complement activity, alongside upregulated expression of immune-related genes (IL-1β, TNF-α, CD4, CD8α, MHC-Iα, IgM) in spleen and hindgut. Our findings establish PLGA microparticles as an effective oral delivery platform and IFN-γ as a potent adjuvant, eliciting robust and durable protection. This study provides a promising strategy for developing effective and scalable oral vaccines against NNV in aquaculture.</p>\",\"PeriodicalId\":12127,\"journal\":{\"name\":\"Fish & shellfish immunology\",\"volume\":\" \",\"pages\":\"110641\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fish & shellfish immunology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1016/j.fsi.2025.110641\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"FISHERIES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fish & shellfish immunology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1016/j.fsi.2025.110641","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/6 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

摘要

由神经坏死病毒(NNV)引起的病毒性神经坏死(VNN)对全球水产养殖构成重大威胁,造成石斑鱼等高价值物种的严重死亡和经济损失。口服疫苗接种提供了大规模预防的实用方法,但面临胃肠道抗原降解和黏膜免疫不足等挑战。为了克服这些问题,我们开发了一种口服DNA疫苗,将编码NNV衣壳蛋白(CP)和IFN-γ的质粒包裹在PLGA微粒中(CPIF@PLGA)。采用双乳液-溶剂蒸发法制备的球形微颗粒(直径约8 μm)包封率高达84.3%。石斑鱼体内免疫试验表明,与对照组相比,CPIF@PLGA显著提高了nnv攻击后的存活率,达到82.2%,降低了脑和眼睛的病毒载量,增强了全身和粘膜免疫。血清IgM、IgT、溶菌酶、SOD和补体活性升高,脾脏和后肠免疫相关基因(IL-1β、TNF-α、CD4、CD8α、MHC-Iα、IgM)表达上调,证明了这一点。我们的研究结果表明,PLGA微粒是一种有效的口服给药平台,IFN-γ是一种有效的佐剂,可以产生强大而持久的保护作用。本研究为在水产养殖中开发有效和可扩展的口服NNV疫苗提供了一个有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral immunization with a DNA vaccine encoding capsid protein and IFN-γ provokes efficient and long-term immunity against nervous necrosis virus.

Viral nervous necrosis (VNN), caused by nervous necrosis virus (NNV), poses a major threat to global aquaculture, causing severe mortality and economic losses in high-value species like grouper. Oral vaccination offers a practical approach for large-scale prevention but faces challenges including gastrointestinal antigen degradation and inadequate mucosal immunity. To overcome these, we developed an oral DNA vaccine by encapsulating a plasmid encoding the NNV capsid protein (CP) and IFN-γ within PLGA microparticles (CPIF@PLGA). Synthesized via double emulsion-solvent evaporation, these spherical microparticles (ca. 8 μm in diameter) exhibited high encapsulation efficiency (84.3 %). In vivo immunization of grouper demonstrated that CPIF@PLGA significantly increased survival to 82.2 % post-NNV challenge versus controls, reduced viral loads in brain and eyes, and enhanced systemic and mucosal immunity. This was evidenced by elevated serum IgM, IgT, lysozyme, SOD, and complement activity, alongside upregulated expression of immune-related genes (IL-1β, TNF-α, CD4, CD8α, MHC-Iα, IgM) in spleen and hindgut. Our findings establish PLGA microparticles as an effective oral delivery platform and IFN-γ as a potent adjuvant, eliciting robust and durable protection. This study provides a promising strategy for developing effective and scalable oral vaccines against NNV in aquaculture.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 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.
×
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