Human metabolome variation along the upper intestinal tract.
Human metabolome variation along the upper intestinal tract.
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DOI:
10.1038/s42255-023-00777-z
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发表时间:
2023-05
影响因子:
20.8
通讯作者:
Fiehn, Oliver
中科院分区:
文献类型:
--
作者:
Folz, Jacob;Culver, Rebecca Neal;Morales, Juan Montes;Grembi, Jessica;Triadafilopoulos, George;Relman, David A.;Huang, Kerwyn Casey;Shalon, Dari;Fiehn, Oliver
Most processing of the human diet occurs in the small intestine. Metabolites in the small intestine originate from host secretions, plus the ingested exposome and microbial transformations. Here we probe the spatiotemporal variation of upper intestinal luminal contents during routine daily digestion in 15 healthy male and female participants. For this, we use a non-invasive, ingestible sampling device to collect and analyse 274 intestinal samples and 60 corresponding stool homogenates by combining five mass spectrometry assays and 16S rRNA sequencing. We identify 1,909 metabolites, including sulfonolipids and fatty acid esters of hydroxy fatty acids (FAHFA) lipids. We observe that stool and intestinal metabolomes differ dramatically. Food metabolites display trends in dietary biomarkers, unexpected increases in dicarboxylic acids along the intestinal tract and a positive association between luminal keto acids and fruit intake. Diet-derived and microbially linked metabolites account for the largest inter-individual differences. Notably, two individuals who had taken antibiotics within 6 months before sampling show large variation in levels of bioactive FAHFAs and sulfonolipids and other microbially related metabolites. From inter-individual variation, we identify Blautia species as a candidate to be involved in FAHFA metabolism. In conclusion, non-invasive, in vivo sampling of the human small intestine and ascending colon under physiological conditions reveals links between diet, host and microbial metabolism. The authors use a non-invasive sampling device to collect intestinal samples in 15 healthy male and female participants and analyse them through mass spectrometry and 16S rRNA sequencing. They identify thousands of biomolecules throughout the intestinal tract, many of which remain unknown and highlight differences between intestinal and stool metabolomes.
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影响因子:
7.4
作者:
Bonini P;Kind T;Tsugawa H;Barupal DK;Fiehn O
通讯作者:
Fiehn O
影响因子:
48
作者:
Callahan BJ;McMurdie PJ;Rosen MJ;Han AW;Johnson AJ;Holmes SP
通讯作者:
Holmes SP
影响因子:
4.2
作者:
GIBSON, GR;CUMMINGS, JH;MACFARLANE, GT
通讯作者:
MACFARLANE, GT
影响因子:
16.6
作者:
Beaudoin GAW;Li Q;Folz J;Fiehn O;Goodsell JL;Angerhofer A;Bruner SD;Hanson AD
通讯作者:
Hanson AD
DOI:
10.1111/j.2517-6161.1995.tb02031.x
发表时间:
1995-01-01
影响因子:
5.8
作者:
BENJAMINI, Y;HOCHBERG, Y
通讯作者:
HOCHBERG, Y