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PROBIOTICS WATCH - Probiotics In Practice

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<strong>PROBIOTICS</strong><br />

<strong>WATCH</strong><br />

ISSUE N°4 2. PHYSIOLOGICAL INTERACTION WITH THE HOST<br />

Contents :<br />

EDITORIAL<br />

THE MAIN POINTS OF<br />

THE QUARTER<br />

1. CHARACTERISATION OF<br />

<strong>PROBIOTICS</strong> AND<br />

PROBIOTIC FOODS<br />

2. PHYSIOLOGICAL<br />

INTERACTION WITH THE<br />

HOST<br />

3. IN VIVO OUTCOMES OF<br />

PROBIOTIC INTAKE<br />

REFERENCES<br />

KEY DATES<br />

2.2. EFFECTS OF <strong>PROBIOTICS</strong> ON MICROBIOTA<br />

Probiotic and nutrient intakes generate specific metabolite<br />

procuction in mice<br />

OBJECTIVES<br />

The complex association of gut flora collectively extends the processing of undigested food to the benefit<br />

of the host through metabolic capacities not encoded in mammalian genomes. At present, metabolic<br />

insights into gut microbiota metabolism remain limited due to the inaccessibility of the intestinal habitat<br />

and gut microbiota complexity. Over the past few decades, the practice of metabonomics has evolved<br />

from diagnosis and identification of biomarkers for a clinical condition towards deciphering the metabolic<br />

predisposition and responses to different individual dietary modulations. The present work monitored<br />

faecal metabolic changes during microbial establishment collected from various groups of mice<br />

supplemented with probiotics or nutrients.<br />

METHODS & MEASURES<br />

1 H-NMR-based metabolic profiling of mouse feces was carried out over time in different microbiome<br />

mouse models, including conventional (n=9), conventionalized (n=10), and “humanized” gnotobiotic<br />

mice inoculated with a model of human baby microbiota (HBM, n=17). HBM mice were supplemented<br />

with Lactobacillus paracasei with (n=10) and without (n=7) prebiotics. Animals not supplemented with<br />

prebiotics received a diet enriched in glucose and lactose as placebo.<br />

RESULTS<br />

<strong>In</strong> conventionalized animals, microbial populations and activities converged in terms of multivariate<br />

mapping toward conventional mice. Both groups decreased bacterial processing of dietary proteins<br />

when switching to a diet enriched in glucose and lactose, as described with low levels of 5-aminovalerate,<br />

acetate, and propionate and high levels of lysine and arginine. The HBM model differs from conventional<br />

and conventionalized microbiota in terms of type, proportion, and metabolic activity of gut bacteria (lower<br />

short chain fatty acids (SCFAs), lactate, 5-aminovalerate, and oligosaccharides, higher bile acids and<br />

choline). The probiotic supplementation of HBM mice was associated with a specific amino acid pattern<br />

that can be linked to L. paracasei proteolytic activities. The combination of L. paracasei with galactosyloligosaccharide<br />

prebiotics was related to the enhanced growth of bifidobacteria and lactobacilli, and a<br />

specific metabolism of carbohydrates, proteins, and SCFAs.<br />

CONCLUSION<br />

The present study describes how the assessment of metabolic changes in feces may provide information<br />

for studying nutrient-microbiota relationships in different microbiome mouse models.<br />

Martin FP, Sprenger N, Montoliu I, Rezzi S, Kochhar S, Nicholson JK. Dietary modulation of gut functional ecology studied by faecal metabonomics.<br />

J Proteome Res. 2010 Oct 1;9(10):5284-95.<br />

6

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