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SyMPaBiome

Financiado

Cerrado

Development of a synbiotic product to modulate the Parkinson s disease associate...

Development of a synbiotic product to modulate the Parkinson s disease associated microbiome SyMPaBiome aims to develop a synbiotic, a mixture of live biotherapeutic bacteria and a prebiotic, to modulate the Parkinson’s disease (PD) microbiome, with the threefold aim to decrease (1) the intestinal (neuro-)inflammation and... ver más

31/12/2023

uni.lu

166K€

Presupuesto del proyecto: 166K€

Líder del proyecto

UNIVERSITE DU LUXEMBOURG No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Fecha límite participación Sin fecha límite de participación.

Financiación concedida El organismo H2020 notifico la concesión del proyecto el día 2023-12-31

WF-03-2020: Widening Fellowships

I+D

Cerrada hace 4 años

0% 100% 100%

Información adicional privada

No hay información privada compartida para este proyecto. Habla con el coordinador.

1 Participantes

uni.lu

166.32K€ | Lider

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Duración del proyecto: 33 meses Fecha Inicio: 2021-03-31
Fecha Fin: 2023-12-31

Líder del proyecto

UNIVERSITE DU LUXEMBOURG No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Presupuesto del proyecto 166K€

Fecha límite de participación Sin fecha límite de participación.

Descripción del proyecto SyMPaBiome aims to develop a synbiotic, a mixture of live biotherapeutic bacteria and a prebiotic, to modulate the Parkinson’s disease (PD) microbiome, with the threefold aim to decrease (1) the intestinal (neuro-)inflammation and (2) gut permeability associated with PD, as well as to (3) decrease the production of a recently discovered archaeal metabolite linked to PD development and progression. This synbiotic regimen will be the first mechanism-based synbiotic formulation, underpinned by functional read-outs from a unique gut-on-a-chip host-microbe interface model. PD is the second most common neurodegenerative disease, and remains incurable. Gastrointestinal symptoms precede the characteristic motor symptoms by years to decades and there is evidence supporting initiation of the disease by enteric inflammation and changes in microbial community composition and function. Enteric inflammation in PD is exacerbated by an increased gut permeability and mucus-foraging bacteria are more abundant in the PD microbiome, while fibre-degrading bacteria are decreased. This offers the opportunity to develop prophylactic or disease-modulating products to address these changes in at-risk individuals or PD patients. Recently, the archaeal metabolite 2-hydroxypyridone (2-HP), a co-factor of the hydrogenase in hydrogenotrophic methanogenic archaea, has been implicated in idiopathic PD aetiology. Here, a preventive or disease modulating strategy is proposed to induce a shift in the microbiome and metabolome of at-risk individuals or PD patients and decrease 2-HP production and its cytotoxic effects on the enteric nervous system. In view of this, we aim to develop a synbiotic product that can restore the metabolic profile and microbial community in PD patients and has a protective effect on the intestinal mucus and epithelium. The outcomes of this project will be a synbiotic formulation, ready for in vivo testing, and a toolbox for mechanism-based development of synbiotic products.

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