纯化的黄芪多糖与灭活疫苗联合使用可显著预防虹鳟鱼(Oncorhynchus mykiss)感染传染性造血坏死病毒。

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Yucai Pan, Zhe Liu, Jinqiang Quan, Wei Gu, Junwei Wang, Guiyan Zhao, Junhao Lu, Jianfu Wang
{"title":"纯化的黄芪多糖与灭活疫苗联合使用可显著预防虹鳟鱼(Oncorhynchus mykiss)感染传染性造血坏死病毒。","authors":"Yucai Pan, Zhe Liu, Jinqiang Quan, Wei Gu, Junwei Wang, Guiyan Zhao, Junhao Lu, Jianfu Wang","doi":"10.1021/acsbiomaterials.4c01478","DOIUrl":null,"url":null,"abstract":"<p><p>Rainbow trout (<i>Oncorhynchus mykiss</i>) is experiencing a catastrophic pandemic. In recent years, infectious hematopoietic necrosis virus (IHNV) has spread nationwide, resulting in significant mortality. Currently, there are no available treatments or vaccines for IHNV in China. Here, the <i>Astragalus</i> extract was purified and characterized. Then, we developed an inactivated IHNV vaccine with purified <i>Astragalus</i> polysaccharide (P-APS) as an adjuvant. Safety assays showed that IHNV was successfully inactivated. After a serious IHNV challenge, the cumulative mortality rates were 76.0, 38.0, and 22.1% in control, vaccine, and P-APS + vaccine groups, respectively. P-APS + vaccine was effective at reducing head kidney damage and apoptosis after IHNV challenge by histopathological and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) analyses. The P-APS + vaccine group showed better results in enhancing specific antibodies (IgM) and immune enzyme activities (C3, LZM, GOT, and GPT). RNA-seq revealed that many immune-related pathways were significantly enriched. <i>TLR2</i>, <i>TLR7</i>, <i>C3</i>, <i>IFN-γ</i>, <i>IgM</i>, <i>MHC1</i>, <i>MHC2</i>, <i>MX1</i>, and <i>VIG1</i> were identified as core genes based on RNA-seq and PPI networks. Mechanistic investigations showed that P-APS + vaccine activates the immune pathway by upregulating the expression of these genes. P-ASP+vaccine induced effective innate and adaptive immune responses that were stronger than single vaccines after vaccination and IHNV challenged. Our findings will provide a promising vaccine candidate against IHNV.</p>","PeriodicalId":8,"journal":{"name":"ACS Biomaterials Science & Engineering","volume":" ","pages":"6938-6953"},"PeriodicalIF":5.4000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Purified <i>Astragalus</i> Polysaccharide Combined with Inactivated Vaccine Markedly Prevents Infectious Haematopoietic Necrosis Virus Infection in Rainbow Trout (<i>Oncorhynchus mykiss</i>).\",\"authors\":\"Yucai Pan, Zhe Liu, Jinqiang Quan, Wei Gu, Junwei Wang, Guiyan Zhao, Junhao Lu, Jianfu Wang\",\"doi\":\"10.1021/acsbiomaterials.4c01478\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Rainbow trout (<i>Oncorhynchus mykiss</i>) is experiencing a catastrophic pandemic. In recent years, infectious hematopoietic necrosis virus (IHNV) has spread nationwide, resulting in significant mortality. Currently, there are no available treatments or vaccines for IHNV in China. Here, the <i>Astragalus</i> extract was purified and characterized. Then, we developed an inactivated IHNV vaccine with purified <i>Astragalus</i> polysaccharide (P-APS) as an adjuvant. Safety assays showed that IHNV was successfully inactivated. After a serious IHNV challenge, the cumulative mortality rates were 76.0, 38.0, and 22.1% in control, vaccine, and P-APS + vaccine groups, respectively. P-APS + vaccine was effective at reducing head kidney damage and apoptosis after IHNV challenge by histopathological and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) analyses. The P-APS + vaccine group showed better results in enhancing specific antibodies (IgM) and immune enzyme activities (C3, LZM, GOT, and GPT). RNA-seq revealed that many immune-related pathways were significantly enriched. <i>TLR2</i>, <i>TLR7</i>, <i>C3</i>, <i>IFN-γ</i>, <i>IgM</i>, <i>MHC1</i>, <i>MHC2</i>, <i>MX1</i>, and <i>VIG1</i> were identified as core genes based on RNA-seq and PPI networks. Mechanistic investigations showed that P-APS + vaccine activates the immune pathway by upregulating the expression of these genes. P-ASP+vaccine induced effective innate and adaptive immune responses that were stronger than single vaccines after vaccination and IHNV challenged. Our findings will provide a promising vaccine candidate against IHNV.</p>\",\"PeriodicalId\":8,\"journal\":{\"name\":\"ACS Biomaterials Science & Engineering\",\"volume\":\" \",\"pages\":\"6938-6953\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2024-11-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Biomaterials Science & Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1021/acsbiomaterials.4c01478\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Biomaterials Science & Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1021/acsbiomaterials.4c01478","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/7 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

摘要

虹鳟鱼(Oncorhynchus mykiss)正在经历一场灾难性的大流行。近年来,传染性造血坏死病毒(IHNV)在全国范围内蔓延,造成大量死亡。目前,中国还没有针对 IHNV 的治疗方法或疫苗。在此,我们对黄芪提取物进行了纯化和表征。然后,我们以纯化的黄芪多糖(P-APS)为佐剂,开发了一种 IHNV 灭活疫苗。安全性试验表明,IHNV 被成功灭活。经过严重的 IHNV 病毒挑战后,对照组、疫苗组和 P-APS + 疫苗组的累积死亡率分别为 76.0%、38.0% 和 22.1%。通过组织病理学和末端脱氧核苷酸转移酶 dUTP 缺口标记(TUNEL)分析,P-APS + 疫苗能有效减少 IHNV 病毒挑战后的头部肾脏损伤和细胞凋亡。P-APS+疫苗组在增强特异性抗体(IgM)和免疫酶活性(C3、LZM、GOT和GPT)方面表现更佳。RNA-seq显示,许多免疫相关通路被显著富集。根据 RNA-seq 和 PPI 网络,TLR2、TLR7、C3、IFN-γ、IgM、MHC1、MHC2、MX1 和 VIG1 被确定为核心基因。机理研究表明,P-ASP+疫苗通过上调这些基因的表达激活了免疫途径。接种P-ASP+疫苗并受到IHNV挑战后,P-ASP+疫苗能诱导有效的先天性和适应性免疫应答,其效果强于单一疫苗。我们的研究结果将为抗击 IHNV 提供一种前景广阔的候选疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Purified Astragalus Polysaccharide Combined with Inactivated Vaccine Markedly Prevents Infectious Haematopoietic Necrosis Virus Infection in Rainbow Trout (Oncorhynchus mykiss).

Rainbow trout (Oncorhynchus mykiss) is experiencing a catastrophic pandemic. In recent years, infectious hematopoietic necrosis virus (IHNV) has spread nationwide, resulting in significant mortality. Currently, there are no available treatments or vaccines for IHNV in China. Here, the Astragalus extract was purified and characterized. Then, we developed an inactivated IHNV vaccine with purified Astragalus polysaccharide (P-APS) as an adjuvant. Safety assays showed that IHNV was successfully inactivated. After a serious IHNV challenge, the cumulative mortality rates were 76.0, 38.0, and 22.1% in control, vaccine, and P-APS + vaccine groups, respectively. P-APS + vaccine was effective at reducing head kidney damage and apoptosis after IHNV challenge by histopathological and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) analyses. The P-APS + vaccine group showed better results in enhancing specific antibodies (IgM) and immune enzyme activities (C3, LZM, GOT, and GPT). RNA-seq revealed that many immune-related pathways were significantly enriched. TLR2, TLR7, C3, IFN-γ, IgM, MHC1, MHC2, MX1, and VIG1 were identified as core genes based on RNA-seq and PPI networks. Mechanistic investigations showed that P-APS + vaccine activates the immune pathway by upregulating the expression of these genes. P-ASP+vaccine induced effective innate and adaptive immune responses that were stronger than single vaccines after vaccination and IHNV challenged. Our findings will provide a promising vaccine candidate against IHNV.

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
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
×
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:481959085
Book学术官方微信