Working Group 3

Extension to diseased situations

Objectives and Activities

The main objective of WG3 is to extend knowledge of in vitro colon models to diseased conditions in both humans and animals, ranging from dysbiosis to other parameters that shape the diseased gut environment.

Working group leaders

Lucie Etienne-Mesmin

WG3 Leader
UMR MEDIS – Université Clermont Auvergne, Clermont-Ferrand

Lidia Tomas-Cobos

WG3 Co-leader
AINIA, Valencia

Tasks

Task 3.1.

Overview on in vitro models adapted to reproduce gut microbiota dysbiosis associated to most common digestive pathologies (IBD, IBS, colon cancer…). Discuss the current limitations of these models in comparison to in vivo situations.

Task 3.2.

Extension of the potential of in vitro gut models to metabolic and non-communicable diseases (metabolic syndrome, obesity, diabetes, steatosis hepatis, coeliac disease…). The main objective is to maintain in vitro microbiota dysbiosis considered as a typical feature of these pathologies in vivo. The associated gut parameters should also be adapted to the specific diseased conditions (pH, transit time, bile acids profiles, nutrient availability...)

Task 3.3.

In vitro gut models can be used to simulate some facets of enteric infection by studying following pathogen inoculation, survival, virulence gene expression and its bilateral interactions with gut microbiota in both upper and lower tract in vitro models

Task 3.4.

In vitro models can be used to evaluate the impact of acute or chronic exposure to food pollutants (chemical, microplastics...) on gut microbiota composition and activity but also reversely the ability of gut microbes to metabolize compounds and modify their toxicity.

Task 3.5.

Pharma therapies and non-antibiotic strategies: evaluate the potential of different restauration strategies (of gut microbiota and metabolic perturbations), such as drugs (under various formulations), but also next generation restoration strategies including prebiotics, probiotics, postbiotics, live biotherapeutic products and fecal microbiota transplantation.

Deliverables

D3.1

Submitted a literature review to identify available diseased in vitro gut models, their limitations and challenges. Due time at month 20

D3.2

Guidelines on which parameters should be considered when developing a new diseased in vitro gut model. Due time at month 32

D3.3

Report on training schools on the way to set up diseased in vitro gut models for young. Due time at month 36

D3.4

Report on a public event to communicate to the scientific community newly available in vitro gut models adapted to diseased situation and present associated results on their development, validation and potential use to test remediation strategies. Due time at month 36

Working group meetings

COST

COST (European Cooperation in Science and Technology) is a funding agency for research and innovation networks. Our Actions help connect research initiatives across Europe and enable scientists to grow their ideas by sharing them with their peers. This boosts their research, career and innovation. (www.cost.eu)

COST Action CA23110

Scientific literature is shedding light on the centrality of GI for human health and wellbeing. Indeed, the physiologic effects of nutrients, bioactives and even toxic compounds (including foodborne pathogens) are mediated by their absorption rate in the intestine and by their interaction with gut microbiota and its host ecosystem. Testing food, feed, supplements or drugs in clinical studies gives rise to ethical issues, and the transferability of animal data across species is often problematic because of differences in physiology, metabolism and chemical susceptibilities.

MoU
062/22

CSO Approval Date
27/05/2022

Start Date
06/10/2022

End Date
05/10/2026

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