Microbiota-dependent influence of prebiotics on the resilience of infant gut microbiota to amoxicillin/clavulanate perturbation in an in vitro colon model

Martha F. Endika, David J. M. Barnett, Cynthia E. Klostermann, Henk A. Schols, Ilja C. W. Arts, John Penders, Arjen Nauta, Hauke Smidt, Koen Venema

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Antibiotic exposure disturbs the developing infant gut microbiota. The capacity of the gut microbiota to recover from this disturbance (resilience) depends on the type of antibiotic. In this study, infant gut microbiota was exposed to a combination of amoxicillin and clavulanate (amoxicillin/clavulanate) in an in vitro colon model (TIM-2) with fecal-derived microbiota from 1-month-old (1-M; a mixed-taxa community type) as well as 3-month-old (3-M; Bifidobacterium dominated community type) breastfed infants. We investigated the effect of two common infant prebiotics, 2′-fucosyllactose (2’-FL) or galacto-oligosaccharides (GOS), on the resilience of infant gut microbiota to amoxicillin/clavulanate-induced changes in microbiota composition and activity. Amoxicillin/clavulanate treatment decreased alpha diversity and induced a temporary shift of microbiota to a community dominated by enterobacteria. Moreover, antibiotic treatment increased succinate and lactate in both 1- and 3-M colon models, while decreasing the production of short-chain (SCFA) and branched-chain fatty acids (BFCA). The prebiotic effect on the microbiota recovery depended on the fermenting capacity of antibiotic-exposed microbiota. In the 1-M colon model, the supplementation of 2’-FL supported the recovery of microbiota and restored the production of propionate and butyrate. In the 3-M colon model, GOS supplementation supported the recovery of microbiota and increased the production of acetate and butyrate.
Original languageEnglish
Article number1131953
JournalFrontiers in Microbiology
Volume14
DOIs
Publication statusPublished - 2023
Externally publishedYes

Funding

We thank Jessica Verhoeven, Sanne Verbruggen, and Rob van Dinter for the technical support during the period of running of TIM-2. We acknowledge Erwin G. Zoetendal for his scientific input during consortium meetings. This study was performed within the public/private partnership coordinated by the Carbohydrate Competence Center (CCC-Carbobiotics) - Grant number ALWCC.2017.011. CarboBiotics is jointly funded by the Dutch Research Council (NWO), FrieslandCampina, AVEBE, and NuScience.

FundersFunder number
Sanne Verbruggen
Nederlandse Organisatie voor Wetenschappelijk Onderzoek

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