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Diet rapidly and reproducibly alters the human gut microbiome

机译:饮食可快速,可重复地改变人类肠道微生物组

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摘要

Long-term dietary intake influences the structure and activity of the trillions of microorganisms residing in the human gut, but it remains unclear how rapidly and reproducibly the human gut microbiome responds to short-term macronutrient change. Here we show that the short-term consumption of diets composed entirely of animal or plant products alters microbial community structure and overwhelms inter-individual differences in microbial gene expression. The animal-based diet increased the abundance of bile-tolerant microorganisms (Alistipes, Rilophila and Bacteroides) and decreased the levels of Firmicutes that metabolize dietary plant polysaccha-rides (Roseburia, Eubacterium rectale and Ruminococcus bromii). Microbial activity mirrored differences between herbivorous and carnivorous mammals, reflecting trade-offs between carbohydrate and protein fermentation. Foodborne microbes from both diets transiently colonized the gut, including bacteria, fungi and even viruses. Finally, increases in the abundance and activity of Bilophila wadsworthia on the animal-based diet support a link between dietary fat, bile acids and the outgrowth of microorganisms capable of triggering inflammatory bowel disease. In concert, these results demonstrate that the gut microbiome can rapidly respond to altered diet, potentially facilitating the diversity of human dietary lifestyles.
机译:长期饮食摄入会影响人类肠道中数以万亿计的微生物的结构和活性,但目前尚不清楚人类肠道微生物组对短期常量营养素变化的反应速度和可重复性如何。在这里,我们表明,短期食用完全由动物或植物产品组成的饮食会改变微生物群落结构,并淹没微生物基因表达的个体差异。以动物为基础的饮食增加了耐胆汁微生物的含量(阿利培斯,里尔菲亚和拟杆菌),并降低了代谢饮食植物多糖(玫瑰红,真细菌和溴化球菌)的硬毛菌素的水平。微生物活动反映了草食性和食肉性哺乳动物之间的差异,反映了碳水化合物和蛋白质发酵之间的权衡。两种饮食中的食源性微生物都会短暂地定居肠道,包括细菌,真菌甚至病毒。最后,以动物为基础的日粮中Badophila wadsworthia的丰度和活性的增加支持了饮食脂肪,胆汁酸和能够触发炎症性肠病的微生物的繁殖之间的联系。一致地,这些结果表明肠道微生物组可以快速响应饮食的变化,从而有可能促进人类饮食生活方式的多样性。

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  • 来源
    《Nature》 |2014年第7484期|559-563|共5页
  • 作者单位

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA,Society of Fellows, Harvard University, Cambridge, Massachusetts 02138, USA,Molecular Genetics & Microbiology and Institute for Genome Sciences & Policy, Duke University, Durham, North Carolina 27708, USA;

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

    Division of Endocrinology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA;

    Department of Bioengineering & Therapeutic Sciences and the California Institute for Quantitative Biosciences, University of California, San Francisco, San Francisco, California 94158, USA;

    Department of Bioengineering & Therapeutic Sciences and the California Institute for Quantitative Biosciences, University of California, San Francisco, San Francisco, California 94158, USA;

    Department of Bioengineering & Therapeutic Sciences and the California Institute for Quantitative Biosciences, University of California, San Francisco, San Francisco, California 94158, USA;

    Division of Endocrinology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA;

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

    FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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