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Updated: Aug 26, 2026

An In Vitro Batch-culture Model to Estimate the Effects of Interventional Regimens on Human Fecal Microbiota
Published on: July 31, 2019
A microbiota-informed pipeline for in vitro characterisation of insulinotropic properties of dairy fermentates using
Enriqueta Garcia-Gutierrez1, Alise J Ponsero2, Víctor Calero3
1Teagasc Food Research Centre, Moorepark, Fermoy, P61 C996 Co, Cork, Ireland.; APC Microbiome Ireland, University College Cork, T12 YN60 Co., Cork, Ireland.; VistaMilk SFI Research Centre, Moorepark, Fermoy, P61 C996 Co., Cork, Ireland; Department of Agronomic Engineering, Technical University of Cartagena, member of European University of Technology EUT+, Paseo Alfonso XIII, 48, 30203 Cartagena, Spain.
Abstract:
Diabetes mellitus (DM), which encompasses Type 1, Type 2 and gestational diabetes, affects approximately 537 million adults, with prevalence continuing to rise. In addition to pregnancy, factors such as dietary choices, lifestyle and infections can lead to the development of DM. Given the increasing prevalence of DM, it is necessary to continue to identify approaches to control the release of insulin. Emerging evidence indicates that the gut microbiota plays a central role in mediating the metabolic effects of diet on the host, including the regulation of insulin secretion. Dietary interventions have been proven to be successful in this regard, but identifying foods and food components that influence insulin secretion is challenging due to the complexity of diet-microbiota-host interactions and the lack of fast and standardised screening tools. We have developed a novel screening framework based on the β-cell insulin response, using the human cell line EndoC-βH1 to assess candidate foods and ingredients with insulinotropic properties. As an initial proof-of-concept, we applied the framework to food ingredients, i.e., dairy-derived fermentates, which had first undergone simulated digestion followed by addition to an ex vivo colon model, allowing us to mimic the metabolic transformations taking place in the human gut. The processed colonic fermentation supernatants were then evaluated using a static and microfluidic platform, respectively, to capture dynamic insulin release profiles. Distinct fermentate compositions were associated with varying levels of insulin secretion. Our results suggest that this framework could be applied broadly to screen foods and food components for insulinotropic potential, providing an affordable approach for the development for anti-diabetic dietary applications.

