Abstract

The human gut microbiota is known for its highly heterogeneous composition across different individuals. However, relatively little is known about functional differences in its ability to ferment complex polysaccharides. Through ex vivo measurements from healthy human donors, we show that individuals vary markedly in their microbial metabolic phenotypes (MMPs), mirroring differences in their microbiota composition, and resulting in the production of different quantities and proportions of Short Chain Fatty Acids (SCFAs) from the same inputs. We also show that aspects of these MMPs can be predicted from composition using 16S rRNA sequencing. From experiments performed using the same dietary fibers in vivo, we demonstrate that an ingested bolus of fiber is almost entirely consumed by the microbiota upon passage. We leverage our ex vivo data to construct a model of SCFA production and absorption in vivo, and argue that inter-individual differences in quantities of absorbed SCFA are directly related to differences in production. Though in vivo studies are required to confirm these data in the context of the gut, in addition to in vivo read outs of SCFAs produced in response to specific fiber spike-ins, these data suggest that optimizing SCFA production in a given individual through targeted fiber supplementation requires quantitative understanding of their MMP.

Highlights

  • The symbiotic relationship between host and gut microbiota is intimately related to host diet

  • We first sought to obtain ex vivo measurements of Short Chain Fatty Acids (SCFAs) production in response to different dietary polysaccharides, in order to quantify the degree of heterogeneity in the fermentation capabilities of the healthy population’s gut microbiota

  • Since we sought to perform the experiments in an environment that best mimicked conditions in the colon, we analyzed 16S rRNA data and determined that community structure or diversity were not significantly altered between timepoints 0 and 4h, with minor changes being observed between 4h and 24h (S4 and S5A Figs)

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Summary

Introduction

The symbiotic relationship between host and gut microbiota is intimately related to host diet. Ruminants derive the majority of their caloric intake from the microbial fermentation of indigestible polysaccharides in their diet. Only a fraction of total caloric intake is derived from fermentation of dietary fibers and other Microbiota Accessible Carbohydrates (MACs), but the resulting metabolites play other important physiological roles [1,2,3]. Following competing interests: E.J.A. is a cofounder and shareholder of Finch Therapeutics, a om pany that specializes in microbiome-targeted therapeutics. This does not alter our adherence to PLOS ONE policies on sharing data and materials

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