• 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

用于口蹄疫病毒研究与诊断的源自猪背侧软腭的原代细胞模型的建立。

Development of a primary cell model derived from porcine dorsal soft palate for foot-and-mouth disease virus research and diagnosis.

作者信息

Sarry Morgan, Bernelin-Cottet Cindy, Michaud Caroline, Relmy Anthony, Romey Aurore, Salomez Anne-Laure, Renson Patricia, Contrant Maud, Berthaud Maxime, Huet Hélène, Jouvion Grégory, Hägglund Sara, Valarcher Jean-François, Bakkali Kassimi Labib, Blaise-Boisseau Sandra

机构信息

UMR VIROLOGIE, INRAe, EnvA, ANSES Laboratoire de Santé Animale, Université Paris-Est, Maisons-Alfort, France.

AgroParistech, Paris, France.

出版信息

Front Microbiol. 2023 Sep 29;14:1215347. doi: 10.3389/fmicb.2023.1215347. eCollection 2023.

DOI:10.3389/fmicb.2023.1215347
PMID:37840704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10570842/
Abstract

Foot-and-mouth disease (FMD) is a highly contagious viral disease of cloven-hoofed animals that has a significant socio-economic impact. One concern associated with this disease is the ability of its etiological agent, the FMD virus (FMDV), to persist in its hosts through underlying mechanisms that remain to be elucidated. While persistence has been described in cattle and small ruminants, it is unlikely to occur in pigs. One of the factors limiting the progress in understanding FMDV persistence and, in particular, differential persistence is the lack of suitable models. A primary bovine cell model derived from the dorsal soft palate, which is the primary site of replication and persistence of FMDV in cattle, has been developed, and it seemed relevant to develop a similar porcine model. Cells from two sites of FMDV replication in pigs, namely, the dorsal soft palate and the oropharyngeal tonsils, were isolated and cultured. The epithelial character of the cells from the dorsal soft palate was then assessed by immunofluorescence. The FMDV-sensitivity of these cells was assessed after monolayer infection with FMDV O/FRA/1/2001 Clone 2.2. These cells were also grown in multilayers at the air-liquid interface to mimic a stratified epithelium susceptible to FMDV infection. Consistent with what has been shown in pigs, our study showed no evidence of persistence of FMDV in either the monolayer or multilayer model, with no infectious virus detected 28 days after infection. The development of such a model opens up new possibilities for the study and diagnosis of FMDV in porcine cells.

摘要

口蹄疫(FMD)是一种偶蹄动物的高度传染性病毒性疾病,具有重大的社会经济影响。与这种疾病相关的一个问题是其病原体口蹄疫病毒(FMDV)通过尚未阐明的潜在机制在宿主中持续存在的能力。虽然在牛和小型反刍动物中已描述了病毒持续存在的情况,但在猪中不太可能发生。限制对口蹄疫病毒持续存在尤其是差异持续存在理解进展的因素之一是缺乏合适的模型。已经开发了一种源自牛背侧软腭的原代牛细胞模型,牛背侧软腭是口蹄疫病毒在牛体内复制和持续存在的主要部位,并且开发类似的猪模型似乎是有意义的。从猪的两个口蹄疫病毒复制部位,即背侧软腭和口咽扁桃体分离并培养细胞。然后通过免疫荧光评估来自背侧软腭的细胞的上皮特征。在用口蹄疫病毒O/FRA/1/2001克隆2.2单层感染后评估这些细胞对口蹄疫病毒的敏感性。这些细胞还在气液界面以多层形式生长,以模拟易受口蹄疫病毒感染的复层上皮。与在猪中所显示的一致,我们的研究表明在单层或多层模型中均没有口蹄疫病毒持续存在的证据,感染后28天未检测到传染性病毒。这种模型的开发为在猪细胞中研究和诊断口蹄疫病毒开辟了新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/4f113b7c8adf/fmicb-14-1215347-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/1f724b982c92/fmicb-14-1215347-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/ddef6b85b1e7/fmicb-14-1215347-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/42df722bd243/fmicb-14-1215347-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/3d2c7288d5f8/fmicb-14-1215347-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/6e15bc21d750/fmicb-14-1215347-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/4536f787c5d7/fmicb-14-1215347-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/214308749ae8/fmicb-14-1215347-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/4f113b7c8adf/fmicb-14-1215347-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/1f724b982c92/fmicb-14-1215347-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/ddef6b85b1e7/fmicb-14-1215347-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/42df722bd243/fmicb-14-1215347-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/3d2c7288d5f8/fmicb-14-1215347-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/6e15bc21d750/fmicb-14-1215347-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/4536f787c5d7/fmicb-14-1215347-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/214308749ae8/fmicb-14-1215347-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/10570842/4f113b7c8adf/fmicb-14-1215347-g008.jpg

相似文献

1
Development of a primary cell model derived from porcine dorsal soft palate for foot-and-mouth disease virus research and diagnosis.用于口蹄疫病毒研究与诊断的源自猪背侧软腭的原代细胞模型的建立。
Front Microbiol. 2023 Sep 29;14:1215347. doi: 10.3389/fmicb.2023.1215347. eCollection 2023.
2
Susceptibility of primary ovine dorsal soft palate and palatine tonsil cells to FMDV infection.绵羊原发性软腭背侧和腭扁桃体细胞对口蹄疫病毒感染的易感性。
Front Vet Sci. 2024 Aug 1;11:1299379. doi: 10.3389/fvets.2024.1299379. eCollection 2024.
3
Model of persistent foot-and-mouth disease virus infection in multilayered cells derived from bovine dorsal soft palate.牛软腭多层细胞中持续性口蹄疫病毒感染模型。
Transbound Emerg Dis. 2020 Jan;67(1):133-148. doi: 10.1111/tbed.13332. Epub 2019 Aug 29.
4
Proteogenomics Uncovers Critical Elements of Host Response in Bovine Soft Palate Epithelial Cells Following In Vitro Infection with Foot-And-Mouth Disease Virus.蛋白质基因组学揭示了牛软腭上皮细胞体外感染口蹄疫病毒后宿主反应的关键因素。
Viruses. 2019 Jan 12;11(1):53. doi: 10.3390/v11010053.
5
The Foot-and-Mouth Disease Carrier State Divergence in Cattle.牛口蹄疫带毒状态的差异
J Virol. 2016 Jun 24;90(14):6344-64. doi: 10.1128/JVI.00388-16. Print 2016 Jul 15.
6
Detection of foot-and-mouth disease virus RNA in pharyngeal epithelium biopsy samples obtained from infected cattle: investigation of possible sites of virus replication and persistence.检测感染牛咽部上皮活检样本中的口蹄疫病毒 RNA:病毒复制和持续存在的可能部位的研究。
Vet Microbiol. 2012 Jan 27;154(3-4):230-9. doi: 10.1016/j.vetmic.2011.07.007. Epub 2011 Jul 20.
7
BacMam Expressing Highly Glycosylated Porcine Interferon Alpha Induces Robust Antiviral and Adjuvant Effects against Foot-and-Mouth Disease Virus in Pigs.BacMam 表达的高度糖基化猪干扰素 α 可在猪中诱导针对口蹄疫病毒的强大抗病毒和佐剂作用。
J Virol. 2022 Jun 22;96(12):e0052822. doi: 10.1128/jvi.00528-22. Epub 2022 May 23.
8
Early events in the pathogenesis of foot-and-mouth disease in pigs; identification of oropharyngeal tonsils as sites of primary and sustained viral replication.猪口蹄疫发病机制中的早期事件;确定口咽扁桃体是病毒初次和持续复制的部位。
PLoS One. 2014 Sep 3;9(9):e106859. doi: 10.1371/journal.pone.0106859. eCollection 2014.
9
Evidence of subclinical foot-and-mouth disease virus infection in young calves born from clinically recovered cow under natural condition.自然条件下临床康复母牛所产犊牛亚临床口蹄疫病毒感染的证据。
Trop Anim Health Prod. 2018 Jun;50(5):1167-1170. doi: 10.1007/s11250-018-1518-6. Epub 2018 Feb 1.
10
Sequences outside that of residues 93-102 of 3A protein can contribute to the ability of foot-and-mouth disease virus (FMDV) to replicate in bovine-derived cells.3A蛋白93 - 102位残基以外的序列可有助于口蹄疫病毒(FMDV)在牛源细胞中复制的能力。
Virus Res. 2014 Oct 13;191:161-71. doi: 10.1016/j.virusres.2014.07.037. Epub 2014 Aug 10.

引用本文的文献

1
Susceptibility of primary ovine dorsal soft palate and palatine tonsil cells to FMDV infection.绵羊原发性软腭背侧和腭扁桃体细胞对口蹄疫病毒感染的易感性。
Front Vet Sci. 2024 Aug 1;11:1299379. doi: 10.3389/fvets.2024.1299379. eCollection 2024.

本文引用的文献

1
Foot-and-Mouth Disease Virus: Molecular Interplays with IFN Response and the Importance of the Model.口蹄疫病毒:分子相互作用与 IFN 反应及模型的重要性。
Viruses. 2022 Sep 27;14(10):2129. doi: 10.3390/v14102129.
2
Trans-Encapsidation of Foot-and-Mouth Disease Virus Genomes Facilitates Escape from Neutralizing Antibodies.口蹄疫病毒基因组的跨囊膜转移有助于逃避中和抗体。
Viruses. 2022 May 27;14(6):1161. doi: 10.3390/v14061161.
3
Foot-and-Mouth Disease Virus Interserotypic Recombination in Superinfected Carrier Cattle.口蹄疫病毒在超级感染带毒牛中的血清型间重组
Pathogens. 2022 Jun 3;11(6):644. doi: 10.3390/pathogens11060644.
4
Vimentin and cytokeratin: Good alone, bad together.波形蛋白和细胞角蛋白:单独很好,一起很糟。
Semin Cancer Biol. 2022 Nov;86(Pt 3):816-826. doi: 10.1016/j.semcancer.2021.12.006. Epub 2021 Dec 22.
5
Evaluation of Cell Lines for the Isolation of Foot-and-Mouth Disease Virus and Other Viruses Causing Vesicular Disease.用于分离口蹄疫病毒及其他引起水疱病病毒的细胞系评估
Front Vet Sci. 2020 Jul 28;7:426. doi: 10.3389/fvets.2020.00426. eCollection 2020.
6
Guidelines and definitions for research on epithelial-mesenchymal transition.上皮-间质转化研究的指南和定义。
Nat Rev Mol Cell Biol. 2020 Jun;21(6):341-352. doi: 10.1038/s41580-020-0237-9. Epub 2020 Apr 16.
7
Foot-and-mouth disease virus: Prospects for using knowledge of virus biology to improve control of this continuing global threat.口蹄疫病毒:利用病毒生物学知识改善对这一持续全球威胁的控制的前景。
Virus Res. 2020 May;281:197909. doi: 10.1016/j.virusres.2020.197909. Epub 2020 Feb 29.
8
Establishment and characterization of the pig tonsil epithelial (PT) cell line as a new model for persist infection of Japanese Encephalitis Virus.建立并鉴定猪扁桃体上皮(PT)细胞系作为日本脑炎病毒持续感染的新型模型。
Vet Microbiol. 2020 Mar;242:108587. doi: 10.1016/j.vetmic.2020.108587. Epub 2020 Jan 18.
9
The Carrier Conundrum; A Review of Recent Advances and Persistent Gaps Regarding the Carrier State of Foot-and-Mouth Disease Virus.携带者难题:口蹄疫病毒携带者状态的最新进展与持续差距综述
Pathogens. 2020 Feb 28;9(3):167. doi: 10.3390/pathogens9030167.
10
Model of persistent foot-and-mouth disease virus infection in multilayered cells derived from bovine dorsal soft palate.牛软腭多层细胞中持续性口蹄疫病毒感染模型。
Transbound Emerg Dis. 2020 Jan;67(1):133-148. doi: 10.1111/tbed.13332. Epub 2019 Aug 29.