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Butyrate-producing Clostridium cluster XIVa species specifically colonize mucins in an in vitro gut model

机译:产生丁酸盐的梭状芽胞杆菌XIVa物种在体外肠道模型中特异性定殖于粘蛋白

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摘要

The human gut is colonized by a complex microbiota with multiple benefits. Although the surface-attached, mucosal microbiota has a unique composition and potential to influence human health, it remains difficult to study in vivo. Therefore, we performed an in-depth microbial characterization (human intestinal tract chip (HITChip)) of a recently developed dynamic in vitro gut model, which simulates both luminal and mucosal gut microbes (mucosal-simulator of human intestinal microbial ecosystem (M-SHIME)). Inter-individual differences among human subjects were confirmed and microbial patterns unique for each individual were preserved in vitro. Furthermore, in correspondence with in vivo studies, Bacteroidetes and Proteobacteria were enriched in the luminal content while Firmicutes rather colonized the mucin layer, with Clostridium cluster XIVa accounting for almost 60% of the mucin-adhered microbiota. Of the many acetate and/or lactate-converting butyrate producers within this cluster, Roseburia intestinalis and Eubacterium rectale most specifically colonized mucins. These 16S rRNA gene-based results were confirmed at a functional level as butyryl-CoA:acetate-CoA transferase gene sequences belonged to different species in the luminal as opposed to the mucin-adhered microbiota, with Roseburia species governing the mucosal butyrate production. Correspondingly, the simulated mucosal environment induced a shift from acetate towards butyrate. As not only inter-individual differences were preserved but also because compared with conventional models, washout of relevant mucin-adhered microbes was avoided, simulating the mucosal gut microbiota represents a breakthrough in modeling and mechanistically studying the human intestinal microbiome in health and disease. Finally, as mucosal butyrate producers produce butyrate close to the epithelium, they may enhance butyrate bioavailability, which could be useful in treating diseases, such as inflammatory bowel disease.
机译:人的肠道被具有多种益处的复杂微生物群定殖。尽管表面附着的粘膜微生物群具有独特的组成和影响人类健康的潜力,但仍然难以在体内进行研究。因此,我们对最近开发的动态体外肠道模型进行了深入的微生物表征(人类肠道芯片(HITChip)),该模型可模拟腔内和黏膜肠道微生物(人类肠道微生物生态系统的黏膜模拟器(M-SHIME) ))。确认了人类受试者之间的个体差异,并在体外保存了每个个体独特的微生物模式。此外,与体内研究相对应,拟杆菌和变形杆菌的腔内含量丰富,而Firmicutes则定居在粘蛋白层,梭状芽胞杆菌XIVa几乎占粘着菌的60%。在该簇中许多乙酸盐和/或乳酸转化的丁酸盐生产者中,小肠玫瑰花菌和真细菌真细菌最特别地定殖于粘蛋白中。这些基于16S rRNA基因的结果在功能水平上得到了证实,因为丁酰辅酶A:乙酸酯辅酶A转移酶基因序列属于管腔中的不同物种,与粘蛋白粘附的菌群相反,而玫瑰果属物种则负责粘膜丁酸的产生。相应地,模拟的粘膜环境引起了从乙酸盐向丁酸盐的转变。由于不仅保留了个体之间的差异,而且因为与传统模型相比,避免了相关粘蛋白粘附的微生物的冲洗,模拟粘膜肠道微生物群代表了在人类肠道微生物组健康和疾病的建模和机理研究方面的突破。最后,由于粘膜丁酸盐生产者在靠近上皮的地方产生丁酸盐,因此它们可以提高丁酸盐的生物利用度,这可用于治疗疾病,例如炎症性肠病。

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