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469 Identification of gut barrier protective fruits and vegetables for Latin American infants

Published online by Cambridge University Press:  11 April 2025

Brian Piccolo
Affiliation:
Arkansas Children’s Nutrition Center
Leslie Tabor-Simecka
Affiliation:
Arkansas Children’s Nutrition Center
Nicole Knox
Affiliation:
Arkansas Children’s Nutrition Center Plants for Human Health Institute, North Carolina State University
Ashley M. McAmis
Affiliation:
Arkansas Children’s Nutrition Center Plants for Human Health Institute, North Carolina State University
Ahmad Ud Din
Affiliation:
Arkansas Children’s Nutrition Center Plants for Human Health Institute, North Carolina State University
Andrew P. Neilson
Affiliation:
Arkansas Children’s Nutrition Center; Department of Biostatistics, University of North
D. Keith Williams
Affiliation:
Arkansas Children’s Nutrition Center; Department of Biostatistics, University of North
Jerry Simecka
Affiliation:
Arkansas for Medical Sciences Department of Pharmaceutical Sciences,
Mario G. Ferruzzi
Affiliation:
University of North Texas Health Science Center Arkansas Children’s Nutrition Center; Department of Pediatrics
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Abstract

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Objectives/Goals: Early childhood obesity is a major concern for Latin American children in the U.S., with gut barrier dysfunction as a key risk factor. Diet plays a role in gut development, but few studies have focused on Latin American infants. Our objective is to identify culturally relevant introductory foods that promote in vitro gut barrier development and function. Methods/Study Population: Pooled human milk (2.5 mL) from 6-month postpartum Hispanic mothers was combined with fruit and vegetable baby food products (2.5 g) and subjected to a 3-phase in vitro digestion system that simulates oral, gastric, and intestinal digestion. Digesta products were then anaerobically fermented for 24-hours using human stool inoculum, centrifuged, and filter sterilized. Intestinal epithelial cells (Caco-2, ATCC) were grown to confluence on 0.4 μm polystyrene transwell inserts using a DMEM + 10% FBS medium and allowed to differentiate for 21-days. Highly differentiated monolayers were treated with a 1:4 dilution of fermenta with medium in triplicate. The cell experiment was conducted twice. Cell layer integrity was measured using transepithelial electrical resistance (TEER) 24- and 48-hours after treatment. Results/Anticipated Results: Dietary intake data from the What We Eat in America database indicated that the top 3 fruit and vegetable exposures for infants with Mexican or Hispanic ethnicity were banana, apple, and carrot. Commercial baby food purees of these fruits and vegetables, in addition to baby foods with blueberry and spinach (Natural for Baby, Gerber Products Company) were acquired for digestion and fermentation experiments. Caco-2 cell experiments with these foods are ongoing. We expect Caco-2 monolayer incubated with fermenta from human milk and fruit or vegetables will have greater TEER values due to increased integrity of the cell layer as compared to those with breast milk alone. We also expect that exposure to fruit and vegetable fermenta will increase gene expression of tight junctions compared to exposure to media and human milk. Discussion/Significance of Impact: Using an in vitro digestion and fermentation system coupled with cell culture studies, we are identifying cellular mechanisms that link individual fruits and vegetables to gut barrier function. This will support translational work focused on mitigating obesity development in vulnerable populations.

Type
Precision Medicine/Health
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - ND
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work.
Copyright
© The Author(s), 2025. The Association for Clinical and Translational Science