Dissection of the host-microbe crosstalk that controls metabolism and physiology in intestinal symbiosis
This project aims to explore the regulatory mechanisms of intestinal bacteria and their symbiotic relationship with hosts using Drosophila to enhance understanding of gut metabolism and health.
Projectdetails
Introduction
Intestinal bacteria have been associated with the most diverse aspects of our physiology, and large efforts are being undertaken to determine how the metabolic repertoire of the microbiome impacts host nutrition and health. These efforts, however, face major obstacles.
Understanding Bacterial Metabolism
First, we have a very poor understanding of how bacterial metabolism is regulated in the different sections of the gastrointestinal tract. It is also becoming increasingly clear that symbionts support their hosts by means that extend beyond the provision of nutrients, and these effects can hardly be predicted from metagenomic analyses.
Research Approaches
We will use ambitious approaches borrowed from several fields, including microbiology, genetics, and cell biology, to dissect how the crosstalk between hosts and their symbionts shapes metabolism and physiology at the scale of the holobiont.
Aim 1 – The Microbe
We will leverage the relevant Drosophila gastrointestinal tract and use multi-omics approaches to dissect, in mechanistic depth, how the metabolism of a model enteric bacterium is regulated in the different sections of the digestive tract.
Aim 2 – The Host
In parallel, our work suggests that symbionts exert a broad control over intestinal digestive and metabolic activities, and act potentially through host bacterial sensing and epigenetic mechanisms to play these roles. We will dissect these regulatory links in Drosophila and investigate their conservation in mammals.
Aim 3 – The Holobiont
Finally, we have evidence that hosts cooperate with their symbionts to regulate gastrointestinal transit, a vital but underappreciated factor that shapes nutrition in both partners. We will use two-sided genetic screens to uncover the bacterial metabolites and the host factors that regulate transit, and determine if this regulation involves the gut-brain axis.
Conclusion
Together, these studies will bring major advances in our understanding of the nutritional and metabolic interactions between hosts and their symbionts.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.499.600 |
Totale projectbegroting | € 1.499.600 |
Tijdlijn
Startdatum | 1-6-2023 |
Einddatum | 31-5-2028 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- RUPRECHT-KARLS-UNIVERSITAET HEIDELBERGpenvoerder
Land(en)
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Resolving metabolic interactions between the gut microbiota and the host with multi-omics-based modelling
This project aims to systematically characterize gut bacteria interactions and their metabolic contributions to host health using experimental and computational methods, enabling targeted microbiota interventions.
Environmental control of physiology through the brain-gut axis
This project aims to investigate how environmental factors influence the brain-gut axis in Drosophila, revealing mechanisms of metabolic adaptation and potential implications for understanding related pathophysiology.
Gut microbiota drug biotransformation as a tool to unravel the mechanisms of metabolic microbiota-host interactions
This project aims to systematically study metabolic interactions between gut microbiota and hosts using drug biotransformation to improve understanding of microbiome-related health variations and drug responses.
T cell regulation by fed state bacterial metabolites
This project aims to identify immunoregulatory bacterial molecules produced in response to food intake, enhancing understanding of gut microbiome tolerance mechanisms and their impact on intestinal health.
Deciphering commensal-host-pathogen metabolic interactions to combat intestinal infections
The GUT-CHECK project aims to elucidate the regulatory mechanisms of polysaccharide utilization loci in Bacteroides to improve understanding of host-pathogen interactions and develop RNA-based therapies for intestinal infections.
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