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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。

Susceptibility of primary ovine dorsal soft palate and palatine tonsil cells to FMDV infection.

作者信息

Sarry Morgan, Laloy Eve, Relmy Anthony, Romey Aurore, Bernelin-Cottet Cindy, Salomez Anne-Laure, Huet Hélène, Hägglund Sara, Valarcher Jean-François, Bakkali Kassimi Labib, Blaise-Boisseau Sandra

机构信息

UMR VIROLOGIE, INRAE, École Nationale Vétérinaire d'Alfort, ANSES Laboratoire de Santé Animale, Université Paris-Est, Maisons-Alfort, France.

AgroParistech, Paris, France.

出版信息

Front Vet Sci. 2024 Aug 1;11:1299379. doi: 10.3389/fvets.2024.1299379. eCollection 2024.

Abstract

Foot and mouth disease (FMD) is a highly contagious viral disease affecting cloven-hoofed animals. This disease is one of the most important in animal health due to its significant socio-economic impact, especially in case of an outbreak. One important challenge associated with this disease is the ability of the FMD virus (FMDV) to persist in its hosts through still unresolved underlying mechanisms. The absence of relevant models is one factor preventing advancement in our understanding of FMDV persistence. While a primary bovine cell model has been established using cells from FMDV primary and persistence site in cattle, it appeared interesting to develop a similar model based on ovine anatomical sites of interest to compare host-pathogen interactions. Thus, epithelial cells derived from the palatine tonsils and the dorsal soft palate were isolated and cultured. Their epithelial nature was confirmed using immunofluorescence. Following monolayer infection with FMDV O/FRA/1/2001 Clone 2.2, the FMDV-sensitivity of these cells was evaluated. Dorsal soft palate (DSP) cells were also expanded in multilayers at the air-liquid interface to mimic a stratified epithelium sensitive to FMDV infection. Our investigation revealed the presence of infectious virus, as well as viral antigens and viral RNA, up to 35 days after infection of the cell multilayers. Further experiment with DSP cells from different individuals needs to be reproduced to confirm the robustness of the new model of persistence in multilayer DSP. The establishment of such primary cells creates new opportunities for FMDV research and analysis in sheep cells.

摘要

口蹄疫(FMD)是一种影响偶蹄动物的高度传染性病毒性疾病。由于其重大的社会经济影响,尤其是在疫情爆发时,该疾病是动物健康领域最重要的疾病之一。与这种疾病相关的一个重要挑战是口蹄疫病毒(FMDV)通过尚未解决的潜在机制在其宿主中持续存在的能力。缺乏相关模型是阻碍我们对口蹄疫病毒持续存在理解取得进展的一个因素。虽然已经利用来自牛的口蹄疫病毒原发和持续存在部位的细胞建立了原代牛细胞模型,但基于绵羊感兴趣的解剖部位开发类似模型以比较宿主 - 病原体相互作用似乎很有意义。因此,分离并培养了源自腭扁桃体和软腭背侧的上皮细胞。使用免疫荧光确认了它们的上皮性质。在用口蹄疫病毒O/FRA/1/2001克隆2.2感染单层细胞后,评估了这些细胞对口蹄疫病毒的敏感性。软腭背侧(DSP)细胞也在气液界面处进行多层扩增,以模拟对口蹄疫病毒感染敏感的复层上皮。我们的研究表明,在细胞多层感染后长达35天仍存在传染性病毒、病毒抗原和病毒RNA。需要重复使用来自不同个体的DSP细胞进行进一步实验,以确认多层DSP中持续存在新模型的稳健性。这种原代细胞的建立为在绵羊细胞中进行口蹄疫病毒研究和分析创造了新机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da44/11324873/4f8f511b18a4/fvets-11-1299379-g0001.jpg

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