Gut metabolites and bacterial community networks during a pilot intervention study with flaxseeds in healthy adult men

SCOPE: Flaxseeds contain the phytoestrogens lignans that must be activated to enterolignans by intestinal bacteria. We investigated the impact of flaxseeds on fecal bacterial communities and their associations with fecal and blood metabolites. METHODS AND RESULTS: Nine healthy male adult subjects in...

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Published inMolecular nutrition & food research Vol. 59; no. 8; pp. 1614 - 1628
Main Authors Lagkouvardos, Ilias, Kläring, Karoline, Heinzmann, Silke S, Platz, Stefanie, Scholz, Birgit, Engel, Karl‐Heinz, Schmitt‐Kopplin, Philippe, Haller, Dirk, Rohn, Sascha, Skurk, Thomas, Clavel, Thomas
Format Journal Article
LanguageEnglish
Published Germany Wiley-VCH 01.08.2015
Blackwell Publishing Ltd
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Summary:SCOPE: Flaxseeds contain the phytoestrogens lignans that must be activated to enterolignans by intestinal bacteria. We investigated the impact of flaxseeds on fecal bacterial communities and their associations with fecal and blood metabolites. METHODS AND RESULTS: Nine healthy male adult subjects ingested 0.3 g/kg/day flaxseeds during 1 week. Gut bacteria as well as blood and fecal metabolites were analyzed. Ingestion of flaxseeds triggered a significant increase in the blood concentration of enterolignans, accompanied by fecal excretion of propionate and glycerol. Overall diversity and composition of dominant fecal bacteria remained individual specific throughout the study. Enterolactone production was linked to the abundance of two molecular species identified as Ruminococcus bromii and Ruminococcus lactaris. Most dominant species of the order Bacteroidales were positively associated with fecal concentrations of either acetic, isovaleric, or isobutyric acid, the latter being negatively correlated with blood levels of triglycerides. The relative sequence abundance of one Gemmiger species (Ruminococcaceae) and of Coprococcus comes (Lachnospiraceae) correlated positively with blood levels of LDL cholesterol and triglycerides, respectively. CONCLUSION: Flaxseeds increase enterolignan production but do not markedly alter fecal metabolome and dominant bacterial communities. The data underline the possible role of members of the family Ruminococcaceae in the regulation of enterolignan production and blood lipids.
Bibliography:http://dx.doi.org/10.1002/mnfr.201500125
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FIGURE S1. Measurement of SCFA by GC. Clear and sharp peaks were observed for all SCFA both using authentic reference compounds (red line) or fecal extracts (blue line; representative sample). The identification of SCFA in the fecal samples was based on relative retention times (compared to the internal standard 4-methylvaleric acid): acetic acid, 0.547 min; propionic acid, 0.640 min; isobutyric acid, 0.675 min; butyric acid, 0.752 min; isovaleric acid, 0.809 min; valeric acid, 0.909 min. FIGURE S2. Individual changes in blood and fecal bacterial parameters overtime during the one-week dietary intervention with flaxseeds (0.3 g/kg/d). P-values were obtained by repeated measures ANOVA and refer to exploratory effects prior to adjustment for multiple testing. FIGURE S3. Stacker plots showing individual and mean sequence proportions of bacterial phyla in the fecal samples. FIGURE S4. Main significant correlations between the occurrences of molecular species (see Table ) and metabolite concentrations in blood, as discussed in the body text. Abbreviations: C2, acetic acid; C4 butyric acid; iC4, isobutyric acid; C5, valeric acid; iC5, isovaleric acid; EL, enterolactone; LDL, LDL cholesterol (low-density lipoprotein); L/H, LDL to HDL ratio; MIR, matairesinol; TG, triglycerides. FIGURE S5. Principal component analysis of aqueous extracts from feces analyzed by NMR spectroscopy. (A) Scores plot of all 27 samples using pareto scaling. Outliers in the two components were grouped as B (P1- and P2-T1) and C (P1 and P3). Covariance-correlation plots of these two groups are shown in panel (B) and (C), to highlight metabolites that drive the separation with all other participants. Group B excreted high levels of glucose. Group C was characterized by an overall different profile with exclusive presence of succinate and 5-aminovalerate and higher levels of short-chain fatty acids, alanine and formate. FIGURE S6. Fecal bacteria associated with NMR-signals for succinate and 5-aminovalerate. Box plots show the relative abundance of three dominant OTUs (S46, Bacteroides fragilis; S55, Clostridium nexile; S577, Ruminococcus gnavus) specific for samples from participant P1 and P3 (n = 6) compared with all other samples (n = 21). The prevalence of OTUs is shown in brackets as total of positive samples/total samples for each participant category. Black squares indicate outliersTables
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ArticleID:MNFR2406
Both authors contributed equally to this work and share first authorship
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ISSN:1613-4125
1613-4133
1613-4133
DOI:10.1002/mnfr.201500125