Department of Disease Control, Moredun Research Institute, Midlothian, United Kingdom.
Department of Vaccines and Diagnostics, Moredun Research Institute, Midlothian, United Kingdom.
Front Cell Infect Microbiol. 2021 Sep 8;11:733811. doi: 10.3389/fcimb.2021.733811. eCollection 2021.
Gastrointestinal (GI) infections in sheep have significant implications for animal health, welfare and productivity, as well as being a source of zoonotic pathogens. Interactions between pathogens and epithelial cells at the mucosal surface play a key role in determining the outcome of GI infections; however, the inaccessibility of the GI tract significantly limits the ability to study such interactions in detail. We therefore developed ovine epithelial organoids representing physiologically important gastric and intestinal sites of infection, specifically the abomasum (analogous to the stomach in monogastrics) and ileum. We show that both abomasal and ileal organoids form self-organising three-dimensional structures with a single epithelial layer and a central lumen that are stable in culture over serial passage. We performed RNA-seq analysis on abomasal and ileal tissue from multiple animals and on organoids across multiple passages and show the transcript profile of both abomasal and ileal organoids cultured under identical conditions are reflective of the tissue from which they were derived and that the transcript profile in organoids is stable over at least five serial passages. In addition, we demonstrate that the organoids can be successfully cryopreserved and resuscitated, allowing long-term storage of organoid lines, thereby reducing the number of animals required as a source of tissue. We also report the first published observations of a helminth infecting gastric and intestinal organoids by challenge with the sheep parasitic nematode , demonstrating the utility of these organoids for pathogen co-culture experiments. Finally, the polarity in the abomasal and ileal organoids can be inverted to make the apical surface directly accessible to pathogens or their products, here shown by infection of apical-out organoids with the zoonotic enteric bacterial pathogen serovar Typhimurium. In summary, we report a simple and reliable culture system for generation and maintenance of small ruminant intestinal and gastric organoids. In line with 3Rs principals, use of such organoids will reduce and replace animals in host-pathogen research.
绵羊的胃肠道(GI)感染对动物的健康、福利和生产力具有重大意义,同时也是人畜共患病病原体的来源。病原体与黏膜表面上皮细胞之间的相互作用在决定 GI 感染的结果方面起着关键作用;然而,由于胃肠道难以接近,大大限制了详细研究这种相互作用的能力。因此,我们开发了代表生理上重要的胃和肠道感染部位的绵羊上皮类器官,特别是真胃(类似于单胃动物的胃)和回肠。我们表明,真胃和回肠类器官都能形成具有单层上皮和中央腔的自组织三维结构,在连续传代培养中稳定。我们对来自多个动物的真胃和回肠组织以及多个传代的类器官进行了 RNA-seq 分析,结果表明,在相同条件下培养的真胃和回肠类器官的转录谱反映了它们的来源组织,并且类器官的转录谱在至少五个连续传代中是稳定的。此外,我们证明类器官可以成功地冷冻保存和复苏,从而允许长期储存类器官系,减少作为组织来源所需的动物数量。我们还报告了首次通过用绵羊寄生线虫感染胃和肠道类器官来挑战寄生虫感染类器官的观察结果,证明了这些类器官在病原体共培养实验中的实用性。最后,真胃和回肠类器官的极性可以反转,使顶端表面直接暴露于病原体或其产物,这里通过感染顶端出的类器官展示了肠致病性细菌病原体鼠伤寒沙门氏菌血清型 Typhimurium 的感染。总之,我们报告了一种简单可靠的小反刍动物肠道和胃类器官的生成和维持培养系统。符合 3R 原则,使用这种类器官将减少和替代宿主-病原体研究中的动物。