Abstract

BackgroundThe study of the gut microbiota (GM) is rapidly moving towards its functional characterization by means of shotgun meta-omics. In this context, there is still no consensus on which microbial functions are consistently and constitutively expressed in the human gut in physiological conditions. Here, we selected a cohort of 15 healthy subjects from a native and highly monitored Sardinian population and analyzed their GMs using shotgun metaproteomics, with the aim of investigating GM functions actually expressed in a healthy human population. In addition, shotgun metagenomics was employed to reveal GM functional potential and to compare metagenome and metaproteome profiles in a combined taxonomic and functional fashion.ResultsMetagenomic and metaproteomic data concerning the taxonomic structure of the GM under study were globally comparable. On the contrary, a considerable divergence between genetic potential and functional activity of the human healthy GM was observed, with the metaproteome displaying a higher plasticity, compared to the lower inter-individual variability of metagenome profiles. The taxon-specific contribution to functional activities and metabolic tasks was also examined, giving insights into the peculiar role of several GM members in carbohydrate metabolism (including polysaccharide degradation, glycan transport, glycolysis, and short-chain fatty acid production). Noteworthy, Firmicutes-driven butyrogenesis (mainly due to Faecalibacterium spp.) was shown to be the metabolic activity with the highest expression rate and the lowest inter-individual variability in the study cohort, in line with the previously reported importance of the biosynthesis of this microbial product for the gut homeostasis.ConclusionsOur results provide detailed and taxon-specific information regarding functions and pathways actively working in a healthy GM. The reported discrepancy between expressed functions and functional potential suggests that caution should be used before drawing functional conclusions from metagenomic data, further supporting metaproteomics as a fundamental approach to characterize the human GM metabolic functions and activities.

Highlights

  • The study of the gut microbiota (GM) is rapidly moving towards its functional characterization by means of shotgun meta-omics

  • In the latest years, the study of the gut microbiota (GM) has been shifting from a mere description of the taxonomic composition, usually obtained through the application of 16S rRNA gene sequencing to fecal samples, to a broader investigation of GM functional potential, made possible by shotgun metagenomics (MG) approaches [1]

  • We carried out a comparative investigation of MG and MP features, in order to identify GM functions consistently expressed within the healthy human cohort under study, taking into account the gene potential of the same GMs

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Summary

Introduction

The study of the gut microbiota (GM) is rapidly moving towards its functional characterization by means of shotgun meta-omics In this context, there is still no consensus on which microbial functions are consistently and constitutively expressed in the human gut in physiological conditions. We selected a cohort of 15 healthy subjects from a native and highly monitored Sardinian population and analyzed their GMs using shotgun metaproteomics, with the aim of investigating GM functions expressed in a healthy human population. A few pioneering studies have presented the analysis of paired metagenomes and metaproteomes in disease-related human cohorts [6, 8], a systematic, comparative investigation of taxonomic and functional features potentially and expressed by the GM of a healthy population has not been described so far. MG and MP data were mined in a comparative fashion in order to (i) find which functional features are actively and consistently expressed by the GM, being needful for the host-GM homeostasis; (ii) identify conserved and variable GM features within the population; and (iii) investigate the specific functional and metabolic contribution of the key GM taxa

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