FP7Individual fellowship2012–2013

SYMOBIGUT · Synergy of milk oligosaccharides and Bifidobacterium infantis in modulating gut epithelial cell function; impact on gut barrier function and the brain-gut axis

FP7 — People (Marie Curie Actions)

Duration
2012-05-01 → 2013-10-31
EU contribution
€121,178
Participants
1
Scheme
MC-IOF

Lines connect the coordinator with its partners.

Results in brief

Synergy of milk oligosaccharides and Bifidobacterium infantis in modulating gut epithelial cell function; impact on gut barrier function and the brain-gut axis

Executive Summary: Obesity, i.e. excess of fat mass, has different faces in humans, from obviously healthy to severely sick people. Even if psychological and social distress due to obesity should not be neglected, complications of obesity, such as metabolic syndrome and cardiovascular risks, constitute a major economic burden to our societies. Our societal, economical and scientific challenge is therefore to unravel the mechanisms leading to complications of obesity in order to find preventive strategies. Gut-related disorders in obesity are key factors in the development of obesity-related metabolic disorders such as hyperphagia and type 2 diabetes. The role of the microbiota in these gut-related disorders is also emerging. The objectives of the SYMOBIGUT project were to acquire knowledge and build a professional network on the effect of obesity on intestinal epithelial cells, gut-brain axis regulation of food intake and gut microbiota on one hand and to evaluate the potential of a combination of probiotic (Bifidobacterium infantis) and prebiotic (bovine milk oligosaccharides (BMO)) to alleviate gut epithelial cells disturbances. Different approaches (in vitro and in vivo) were used to study the effect of the combination of B.infantis with BMO on gut barrier function on one hand and on entero-endocrine cells signaling to the brain through the vagus nerve on the other hand. This project was part of a multi-disciplinary project within the Food For Health Institute at UC Davis, California, USA. I established that supplementation of the diet with BMO and B. infantis both prevented or restored gut barrier function in a model of diet-induced obesity in mice. This beneficial effect of this combination is likely due to restoration of gut microbiota and increased level of known beneficial bacteria. I also demonstrated that supernatants obtained from B.infantis culture with BMO but not lactose activates entero-endocrine cells both in vitro and in situ. Gavage of this supernatant to rats resulted in activation of neurons located in nodose ganglia (vagal afferents) and reduction of food intake. Taken together, these final results demonstrate the powerful ability of the combination of B.infantis and BMO to prevent and treat gut-related disorders associated with obesity, i.e. gut barrier function and alteration gut-brain axis signaling. This multi-disciplinary project resulted in a long-term collaboration between the out-going and the return phase groups with exchange of graduate students between labs in the near future. The fellow has now established an independent group with several graduate students and grant application under examination. Expected impact are the use of the combination of probiotic and prebiotic in prevention and treatment of gut-related disorders in obesity on one hand and long-term collaboration between the two labs on the other hand.

Data: CORDIS, © European Union

Project objective

The role of gut microbiota in modulating the brain-gut axis and in control of food intake and obesity has recently emerged. My out-going phase host, Dr Raybould at UC Davis (USA), is an internationally renowned scientist in the field of gut chemosensing by entero-endocrine cells (EEC) and signalling to the brain through vagal afferents. Preliminary experiments in her laboratory demonstrate a synergetic effect of milk oligosaccharides (MO) and a commensal bacteria, Bifdobacterium infantis in activating EEC. Using a multi-disciplinary approach and state-of-the art techniques, I aim to investigate i) how MO potentiate adhesion of B. infantis on epithelial cells through specific surface proteins and ii) what are the functional consequences at the intestinal epithelial cells and the brain-gut axis levels of such interactions. This will train me in methods and knowledge on EEC and vagal afferent signaling which I need to get in order to lead a small scientific group in the newly created ADNC unit at INRA, Rennes (France). This innovative project will provide basic knowledge on microbiota-EEC-vagal afferent interactions critical in the understanding of obesity and metabolic disorders, chronic diseases which are becoming a burden in our societies. It is also a unique ability for Europe to accelerate translation of a protective mechanism from human milk into wide-reaching nutritional strategies aimed at gut and metabolic health in humans. Moreover, the complementary skills (management of a multi-disciplinary project, student supervision, grant writing and creation of a multidisciplinary network within the Milk Bioactive Program at UC Davis) I will be trained in, ensured by the mentoring experience and the highly interactive environment of both host laboratories, will reinforce my position as a group leader in the ADNC unit. The proposed project is a great opportunity for Europe to support and prepare a young researcher to become a group leader in gut neurophysiology.""

Original text from CORDIS.

Participants

  • INSTITUT NATIONAL DE RECHERCHE POUR L'AGRICULTURE, L'ALIMENTATION ET L'ENVIRONNEMENT · ParisCoordinatorFrance

Links

Data: CORDIS, © European Union