• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于研究口蹄疫的实验动物模型:一篇重点关注天然免疫和疫苗诱导免疫的综述

Laboratory animal models to study foot-and-mouth disease: a review with emphasis on natural and vaccine-induced immunity.

作者信息

Habiela Mohammed, Seago Julian, Perez-Martin Eva, Waters Ryan, Windsor Miriam, Salguero Francisco J, Wood James, Charleston Bryan, Juleff Nicholas

机构信息

Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge CB3 0ES, UK.

The Pirbright Institute, Ash Road, Woking, Surrey GU24 0NF, UK.

出版信息

J Gen Virol. 2014 Nov;95(Pt 11):2329-2345. doi: 10.1099/vir.0.068270-0. Epub 2014 Jul 7.

DOI:10.1099/vir.0.068270-0
PMID:25000962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4202264/
Abstract

Laboratory animal models have provided valuable insight into foot-and-mouth disease virus (FMDV) pathogenesis in epidemiologically important target species. While not perfect, these models have delivered an accelerated time frame to characterize the immune responses in natural hosts and a platform to evaluate therapeutics and vaccine candidates at a reduced cost. Further expansion of these models in mice has allowed access to genetic mutations not available for target species, providing a powerful and versatile experimental system to interrogate the immune response to FMDV and to target more expensive studies in natural hosts. The purpose of this review is to describe commonly used FMDV infection models in laboratory animals and to cite examples of when these models have failed or successfully provided insight relevant for target species, with an emphasis on natural and vaccine-induced immunity.

摘要

实验动物模型为深入了解口蹄疫病毒(FMDV)在具有重要流行病学意义的目标物种中的发病机制提供了宝贵的见解。尽管这些模型并非完美无缺,但它们缩短了表征天然宿主免疫反应所需的时间,并提供了一个以较低成本评估治疗方法和候选疫苗的平台。在小鼠中对这些模型的进一步扩展,使得能够利用目标物种所没有的基因突变,从而提供了一个强大且通用的实验系统,用于探究针对FMDV的免疫反应,并针对天然宿主中更昂贵的研究进行靶向研究。本综述的目的是描述实验动物中常用的FMDV感染模型,并列举这些模型失败或成功提供与目标物种相关见解的实例,重点是天然免疫和疫苗诱导的免疫。

相似文献

1
Laboratory animal models to study foot-and-mouth disease: a review with emphasis on natural and vaccine-induced immunity.用于研究口蹄疫的实验动物模型:一篇重点关注天然免疫和疫苗诱导免疫的综述
J Gen Virol. 2014 Nov;95(Pt 11):2329-2345. doi: 10.1099/vir.0.068270-0. Epub 2014 Jul 7.
2
Duration of protection and humoral immunity induced by an adenovirus-vectored subunit vaccine for foot-and-mouth disease (FMD) in Holstein steers.牛传染性口蹄疫(FMD)腺病毒载体亚单位疫苗诱导的保护持续时间和体液免疫。
Vaccine. 2019 Sep 30;37(42):6221-6231. doi: 10.1016/j.vaccine.2019.08.017. Epub 2019 Sep 5.
3
Combined administration of synthetic RNA and a conventional vaccine improves immune responses and protection against foot-and-mouth disease virus in swine.合成RNA与传统疫苗联合给药可改善猪对口蹄疫病毒的免疫反应并提供保护。
Antiviral Res. 2017 Jun;142:30-36. doi: 10.1016/j.antiviral.2017.03.009. Epub 2017 Mar 16.
4
Recombinant adenovirus expressing type Asia1 foot-and-mouth disease virus capsid proteins induces protective immunity against homologous virus challenge in mice.表达亚洲 1 型口蹄疫病毒衣壳蛋白的重组腺病毒在小鼠中诱导针对同源病毒攻击的保护性免疫。
Res Vet Sci. 2013 Jun;94(3):796-802. doi: 10.1016/j.rvsc.2012.12.004. Epub 2012 Dec 23.
5
Increased efficacy of an adenovirus-vectored foot-and-mouth disease capsid subunit vaccine expressing nonstructural protein 2B is associated with a specific T cell response.表达非结构蛋白 2B 的腺病毒载体口蹄疫衣壳亚单位疫苗的效力增加与特定的 T 细胞反应有关。
Vaccine. 2011 Nov 28;29(51):9431-40. doi: 10.1016/j.vaccine.2011.10.037. Epub 2011 Oct 24.
6
Co-expression of the Bcl-xL antiapoptotic protein enhances the induction of Th1-like immune responses in mice immunized with DNA vaccines encoding FMDV B and T cell epitopes.Bcl-xL 抗凋亡蛋白的共表达增强了用编码 FMDV B 和 T 细胞表位的 DNA 疫苗免疫的小鼠中 Th1 样免疫应答的诱导。
Vet Res Commun. 2013 Sep;37(3):187-96. doi: 10.1007/s11259-013-9560-3. Epub 2013 Mar 13.
7
Chimeric Porcine Parvovirus VP2 Virus-like Particles with Epitopes of South African Serotype 2 Foot-and-Mouth Disease Virus Elicits Specific Humoral and Cellular Responses in Mice.带有南非2型口蹄疫病毒表位的嵌合猪细小病毒VP2病毒样颗粒在小鼠中引发特异性体液和细胞免疫反应。
Viruses. 2024 Apr 17;16(4):621. doi: 10.3390/v16040621.
8
DNA vaccines expressing B and T cell epitopes can protect mice from FMDV infection in the absence of specific humoral responses.表达B细胞和T细胞表位的DNA疫苗能够在缺乏特异性体液免疫反应的情况下保护小鼠免受口蹄疫病毒感染。
Vaccine. 2006 May 1;24(18):3889-99. doi: 10.1016/j.vaccine.2006.02.028. Epub 2006 Mar 3.
9
Characterization of cytotoxic T lymphocyte function after foot-and-mouth disease virus infection and vaccination.口蹄疫病毒感染和疫苗接种后细胞毒性 T 淋巴细胞功能的特征。
Viral Immunol. 2013 Aug;26(4):239-49. doi: 10.1089/vim.2013.0011. Epub 2013 Jul 5.
10
Expression of the VP1 protein of FMDV integrated chromosomally with mutant Listeria monocytogenes strain induced both humoral and cellular immune responses.表达 FMDV 的 VP1 蛋白与突变李斯特菌菌株整合的染色体诱导体液和细胞免疫反应。
Appl Microbiol Biotechnol. 2019 Feb;103(4):1919-1929. doi: 10.1007/s00253-018-09605-x. Epub 2019 Jan 9.

引用本文的文献

1
Qualitative Risk Assessment of Foot-and-Mouth Disease Virus Introduction and Transmission to Dairy Farms via Raw Milk Transportation in Thailand: A Scenario-Based Approach.泰国口蹄疫病毒通过生乳运输传入和传播至奶牛场的定性风险评估:基于情景的方法
Vet Sci. 2025 Jun 27;12(7):623. doi: 10.3390/vetsci12070623.
2
Assessment of PRRSV and PCV2 seroprevalence and antigen prevalence in minipigs at laboratory-animal production facilities.实验动物生产设施中微型猪的猪繁殖与呼吸综合征病毒(PRRSV)和猪圆环病毒2型(PCV2)血清阳性率及抗原阳性率评估
J Adv Vet Anim Res. 2024 Dec 28;11(4):1017-1022. doi: 10.5455/javar.2024.k852. eCollection 2024 Dec.
3
Serological Conversion through a Second Exposure to Inactivated Foot-and-Mouth Disease Virus Expressing the JC Epitope on the Viral Surface.通过再次接触在病毒表面表达 JC 表位的灭活口蹄疫病毒实现血清学转换。
Vaccines (Basel). 2023 Sep 14;11(9):1487. doi: 10.3390/vaccines11091487.
4
Recombinant-attenuated Salmonella enterica serovar Choleraesuis vector expressing the PlpE protein of Pasteurella multocida protects mice from lethal challenge.表达多杀性巴氏杆菌 PlpE 蛋白的重组减毒猪霍乱沙门氏菌载体可保护小鼠免受致死性攻击。
BMC Vet Res. 2023 Aug 19;19(1):128. doi: 10.1186/s12917-023-03679-0.
5
Generating a Heat-Tolerance Mouse Model.生成耐热小鼠模型。
Methods Mol Biol. 2022;2495:259-272. doi: 10.1007/978-1-0716-2301-5_14.
6
Foot-and-mouth disease virus localisation on follicular dendritic cells and sustained induction of neutralising antibodies is dependent on binding to complement receptors (CR2/CR1).口蹄疫病毒在滤泡树突状细胞上的定位和持续诱导中和抗体的产生依赖于与补体受体(CR2/CR1)的结合。
PLoS Pathog. 2022 May 5;18(5):e1009942. doi: 10.1371/journal.ppat.1009942. eCollection 2022 May.
7
Vaccines as a Strategy to Control Trichinellosis.疫苗作为控制旋毛虫病的一种策略。
Front Microbiol. 2022 Mar 23;13:857786. doi: 10.3389/fmicb.2022.857786. eCollection 2022.
8
Interleukin-10-Mediated Lymphopenia Caused by Acute Infection with Foot-and-Mouth Disease Virus in Mice.急性感染口蹄疫病毒导致小鼠白细胞介素 10 介导的淋巴细胞减少症。
Viruses. 2021 Nov 24;13(12):2358. doi: 10.3390/v13122358.
9
Ribavirin as a curative and prophylactic agent against foot and mouth disease virus infection in C57BL/6 suckling and adult mice model.利巴韦林作为治疗和预防剂对C57BL/6乳鼠和成年小鼠模型中口蹄疫病毒感染的作用
Virusdisease. 2021 Dec;32(4):737-747. doi: 10.1007/s13337-021-00746-8. Epub 2021 Oct 20.
10
Transboundary Animal Diseases, an Overview of 17 Diseases with Potential for Global Spread and Serious Consequences.跨界动物疾病:17种可能全球传播并造成严重后果的疾病概述
Animals (Basel). 2021 Jul 8;11(7):2039. doi: 10.3390/ani11072039.

本文引用的文献

1
Selection of foot and mouth disease antisera for diagnosis by ELISA.用于酶联免疫吸附测定(ELISA)诊断的口蹄疫抗血清的选择
Rev Sci Tech. 1988 Jan;7(2):331-346. doi: 10.20506/rst.7.2.347.
2
Type III interferon protects swine against foot-and-mouth disease.III型干扰素可保护猪免受口蹄疫侵害。
J Interferon Cytokine Res. 2014 Oct;34(10):810-21. doi: 10.1089/jir.2013.0112. Epub 2014 Apr 30.
3
Foot-and-mouth disease virus virulence in cattle is co-determined by viral replication dynamics and route of infection.口蹄疫病毒在牛中的毒力由病毒复制动力学和感染途径共同决定。
Virology. 2014 Mar;452-453:12-22. doi: 10.1016/j.virol.2014.01.001. Epub 2014 Jan 25.
4
3Cpro of foot-and-mouth disease virus antagonizes the interferon signaling pathway by blocking STAT1/STAT2 nuclear translocation.3Cpro 蛋白通过阻断 STAT1/STAT2 核转位来拮抗口蹄疫病毒的干扰素信号通路。
J Virol. 2014 May;88(9):4908-20. doi: 10.1128/JVI.03668-13. Epub 2014 Feb 19.
5
Reshaping antibody diversity.重塑抗体多样性。
Cell. 2013 Jun 6;153(6):1379-93. doi: 10.1016/j.cell.2013.04.049.
6
Virus-induced humoral immunity: on how B cell responses are initiated.病毒诱导的体液免疫:B 细胞应答的启动机制。
Curr Opin Virol. 2013 Jun;3(3):357-62. doi: 10.1016/j.coviro.2013.05.004. Epub 2013 Jun 1.
7
T-bet and Gata3 in controlling type 1 and type 2 immunity mediated by innate lymphoid cells.T-bet 和 Gata3 在先天淋巴细胞介导的 1 型和 2 型免疫反应中的调控作用。
Curr Opin Immunol. 2013 Apr;25(2):139-47. doi: 10.1016/j.coi.2013.02.007. Epub 2013 Mar 13.
8
Venezuelan equine encephalitis replicon particles can induce rapid protection against foot-and-mouth disease virus.委内瑞拉马脑炎复制子颗粒能快速诱导对口蹄疫病毒的保护。
J Virol. 2013 May;87(10):5447-60. doi: 10.1128/JVI.03462-12. Epub 2013 Mar 6.
9
Early adaptive immune responses in the respiratory tract of foot-and-mouth disease virus-infected cattle.口蹄疫病毒感染牛呼吸道中的早期适应性免疫反应。
J Virol. 2013 Mar;87(5):2489-95. doi: 10.1128/JVI.02879-12. Epub 2012 Dec 19.
10
CD4+ T-cell responses to foot-and-mouth disease virus in vaccinated cattle.接种牛口蹄疫病毒后 CD4+ T 细胞的反应。
J Gen Virol. 2013 Jan;94(Pt 1):97-107. doi: 10.1099/vir.0.045732-0. Epub 2012 Oct 3.