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Microbial Community Development in a Dynamic Gut Model Is Reproducible, Colon Region Specific, and Selective for Bacteroidetes and Clostridium Cluster IX

机译:动态肠道模型中的微生物群落发育是可复制的,结肠区域特定的,并且对拟杆菌和梭状芽胞杆菌第九类具有选择性

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Dynamic, multicompartment in vitro gastrointestinal simulators are often used to monitor gut microbial dynamics and activity. These reactors need to harbor a microbial community that is stable upon inoculation, colon region specific, and relevant to in vivo conditions. Together with the reproducibility of the colonization process, these criteria are often overlooked when the modulatory properties from different treatments are compared. We therefore investigated the microbial colonization process in two identical simulators of the human intestinal microbial ecosystem (SHIME), simultaneously inoculated with the same human fecal microbiota with a high-resolution phylogenetic microarray: the human intestinal tract chip (HITChip). Following inoculation of the in vitro colon compartments, microbial community composition reached steady state after 2 weeks, whereas 3 weeks were required to reach functional stability. This dynamic colonization process was reproducible in both SHIME units and resulted in highly diverse microbial communities which were colon region specific, with the proximal regions harboring saccharolytic microbes (e.g., Bacteroides spp. and Eubacterium spp.) and the distal regions harboring mucin-degrading microbes (e.g., Akkermansia spp.). Importantly, the shift from an in vivo to an in vitro environment resulted in an increased Bacteroidetes / Firmicutes ratio, whereas Clostridium cluster IX (propionate producers) was enriched compared to clusters IV and XIVa (butyrate producers). This was supported by proportionally higher in vitro propionate concentrations. In conclusion, high-resolution analysis of in vitro -cultured gut microbiota offers new insight on the microbial colonization process and indicates the importance of digestive parameters that may be crucial in the development of new in vitro models.
机译:动态的多室体外胃肠道模拟器通常用于监测肠道微生物的动力学和活性。这些反应器需要带有一个微生物群落,该微生物群落在接种后是稳定的,结肠区域是特定的,并且与体内条件有关。与定殖过程的可重复性一起,当比较不同处理方法的调节特性时,通常会忽略这些标准。因此,我们在人类肠道微生物生态系统(SHIME)的两个相同的模拟器中研究了微生物定殖过程,同时用同一人类粪便微生物菌群同时接种了高分辨率的系统进化芯片:人类肠道芯片(HITChip)。接种体外结肠区室后,微生物群落组成在2周后达到稳定状态,而需要3周才能达到功能稳定性。该动态定殖过程在两个SHIME单元中均可重现,并导致了特定于结肠区域的高度多样化的微生物群落,其中近端区域带有糖酵解微生物(例如,拟杆菌和真细菌),而远端区域则带有降解黏蛋白的微生物。 (例如Akkermansia spp。)。重要的是,从体内环境向体外环境的转移导致了拟杆菌/硬菌比的增加,而相比于IV和XIVa群(丁酸酯生产者),梭状芽孢杆菌第IX簇(丙酸酯生产者)得到了富集。比例较高的体外丙酸盐浓度对此提供了支持。总之,对体外培养的肠道菌群的高分辨率分析为微生物定殖过程提供了新的见识,并表明了消化参数的重要性,这对于开发新的体外模型至关重要。

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