Department of Gastroenterology and Hepatology, Erasmus MC-University Medical Center, Rotterdam, Netherlands.
Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, TEDA Institute of Biological Sciences and Biotechnology, Nankai University, Tianjin, China.
Front Cell Infect Microbiol. 2018 Apr 4;8:102. doi: 10.3389/fcimb.2018.00102. eCollection 2018.
are Gram-negative rod-shaped facultative anaerobic bacteria that are comprised of over 2,000 serovars. They cause gastroenteritis (salmonellosis) with headache, abdominal pain and diarrhea clinical symptoms. Salmonellosis brings a heavy burden for the public health in both developing and developed countries. Antibiotics are usually effective in treating the infected patients with severe gastroenteritis, although antibiotic resistance is on the rise. Understanding the molecular mechanisms of infection is vital to combat the disease. immortalized 2-D cell lines, tissues/organs and several animal models have been successfully utilized to study infections. Although these infection models have contributed to uncovering the molecular virulence mechanisms, some intrinsic shortcomings have limited their wider applications. Notably, cell lines only contain a single cell type, which cannot reproduce some of the hallmarks of natural infections. While tissues/organs alleviate some of these concerns, they are more difficult to maintain, in particular for long term experiments. In addition, non-human animal models are known to reflect only part of the human disease process. Enteroids and induced intestinal organoids are emerging as effective infection models due to their closeness in mimicking the infected tissues/organs. Induced intestinal organoids are derived from iPSCs and contain mesenchymal cells whereas enteroids are derive from intestinal stem cells and are comprised of epithelial cells only. Both enteroids and induced intestinal organoids mimic the villus and crypt domains comparable to the architectures of the intestine. We review here that enteroids and induced intestinal organoids are emerging as desired infection models to study bacterial-host interactions of .
它们是革兰氏阴性杆状兼性厌氧菌,由超过 2000 个血清型组成。它们引起头痛、腹痛和腹泻等临床症状的胃肠炎(沙门氏菌病)。沙门氏菌病给发展中国家和发达国家的公共卫生都带来了沉重的负担。抗生素通常对治疗严重胃肠炎的感染患者有效,尽管抗生素耐药性正在上升。了解感染的分子机制对于对抗这种疾病至关重要。
永生化的 2D 细胞系、组织/器官和几种动物模型已成功用于研究感染。虽然这些感染模型有助于揭示分子毒力机制,但它们的一些内在局限性限制了它们的更广泛应用。值得注意的是,细胞系仅包含单一细胞类型,无法复制自然感染的一些特征。虽然组织/器官缓解了其中的一些问题,但它们更难维持,特别是对于长期实验。此外,非人类动物模型已知只能反映人类疾病过程的一部分。由于其在模拟感染组织/器官方面的接近度,类器官和诱导性肠类器官正在成为有效的感染模型。诱导性肠类器官源自 iPSCs 并包含间质细胞,而类器官则源自肠干细胞,仅由上皮细胞组成。类器官和诱导性肠类器官都模拟了与小肠结构相当的绒毛和隐窝结构。我们在这里回顾了类器官和诱导性肠类器官正在成为研究的细菌-宿主相互作用的理想感染模型。