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在模拟肠上皮的共培养模型中阻止海德堡易位。

prevents Heidelberg translocation in co-culture model mimicking intestinal epithelium.

作者信息

Vernay T, Cannie I, Gaboriau F, Gall S David-Le, Tamanai-Shacoori Z, Burel A, Jolivet-Gougeon A, Loréal O, Bousarghin L

机构信息

INSERM, Univ Rennes, INRAE, CHU Rennes, Nutrition Metabolisms and Cancer (NuMeCan), UMR-1241, Biosit, MRic/ISFR, 2 rue Henri Le Guilloux, 35033 Rennes, France.

Plateforme microscopie électronique MRic/ISFR Biosit/campus Santé, Rennes 1, 2 Avenue du Professeur Léon Bernard, 35000 Rennes, France.

出版信息

Benef Microbes. 2020 Aug 12;11(4):391-401. doi: 10.3920/BM2020.0004. Epub 2020 Jul 28.

DOI:10.3920/BM2020.0004
PMID:32720833
Abstract

Heidelberg is one of the most common serovar causing foodborne illnesses. To limit the development of digestive bacterial infection, food supplements containing probiotic bacteria can be proposed. Commensal non-toxigenic has recently been suggested as a next-generation probiotic candidate. By using an original triple co-culture model including Caco-2 cells (representing human enterocytes), HT29-MTX (representing mucus-secreting goblet cells), and M cells differentiated from Caco-2 by addition of Raji B lymphocytes, bacterial translocation was evaluated. The data showed that Heidelberg could translocate in the triple co-culture model with high efficiency, whereas for a weak translocation was obtained. When cells were exposed to both bacteria, Heidelberg translocation was inhibited. The cell-free supernatant of also inhibited Heidelberg translocation without impacting epithelial barrier integrity. This supernatant did not affect the growth of Heidelberg. The non-toxigenic confers health benefits to the host by reducting bacterial translocation. These results suggested that the multicellular model provides an efficient model to evaluate the translocation of pathogens and to screen for probiotics that have a potential inhibitory effect on this translocation.

摘要

海德堡菌是引起食源性疾病最常见的血清型之一。为限制消化细菌感染的发展,可推荐含有益生菌的食品补充剂。共生无毒菌株最近被认为是下一代益生菌候选菌株。通过使用一种原始的三重共培养模型,该模型包括Caco-2细胞(代表人类肠上皮细胞)、HT29-MTX细胞(代表分泌黏液的杯状细胞)以及通过添加Raji B淋巴细胞从Caco-2细胞分化而来的M细胞,对细菌移位进行了评估。数据显示,海德堡菌在三重共培养模型中能够高效移位,而对于[此处原文缺失相关细菌名称],移位效率较低。当细胞同时暴露于这两种细菌时,海德堡菌的移位受到抑制。[此处原文缺失相关细菌名称]的无细胞上清液也抑制了海德堡菌的移位,且不影响上皮屏障的完整性。这种上清液不影响海德堡菌的生长。无毒[此处原文缺失相关细菌名称]通过减少细菌移位为宿主带来健康益处。这些结果表明,该多细胞模型为评估病原体的移位以及筛选对这种移位具有潜在抑制作用的益生菌提供了一种有效的模型。

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