4.7 Article

Influence of short-term changes in dietary sulfur on the relative abundances of intestinal sulfate-reducing bacteria

期刊

GUT MICROBES
卷 10, 期 4, 页码 447-457

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/19490976.2018.1559682

关键词

Sulfate-reducing bacteria; 16S rRNA gene; shotgun metagenomics; dietary sulfur

资金

  1. Allen Foundation
  2. Hubbard Broadcasting Foundation
  3. Healthy Foods, Healthy Lives
  4. Achieving Cures Together

向作者/读者索取更多资源

High-protein diets may be linked to gut inflammation due to increased production of hydrogen sulfide (H2S), a potential toxin, as an end product of microbial fermentation in the colon by sulfidogenic sulfate-reducing bacteria (SRB). We hypothesized that dietary content of sulfur-containing amino acids (SAA) leads to variation in the relative abundances of intestinal SRB, which include Desulfovibrio and Bilophila taxa. To test this hypothesis we performed a pilot crossover study in four healthy volunteers, who consumed two interventional diets for 10-14 days, containing high or low SAA content. The total energy intake was similar between the two dietary extremes. Microbial communities were characterized by 16S rRNA gene amplicon and shotgun next-generation DNA sequencing. While the relative abundance of Desulfovibrio differed among participants (ANOVA P= 0.001), we could not detect a change with dietary treatments. Similarly, no differences in Bilophila abundance were observed among individuals or dietary arms. Inter-personal differences in microbial community composition and functional gene categories differed between subjects and these differences were maintained over the course of the study. These observations are consistent with re-analysis of two previously published dietary intervention studies. Finally, we found that inter-personal differences in the taxonomic composition of fecal microbiota, including the relative abundances of SRB, were maintained over time in 19 healthy individuals in our stool donor program. These results suggest that the use of dietary interventions alone may be insufficient for rapid therapeutic targeting of SRB. Nevertheless, these pilot data provide a foundation to inform future, statistically powered, studies.

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