Abstract

The human intestinal tract is colonized by microbial communities that show a subject-specific composition and a high-level temporal stability in healthy adults. To determine whether this is reflected at the functional level, we compared the faecal metaproteomes of healthy subjects over time using a novel high-throughput approach based on denaturing polyacrylamide gel electrophoresis and liquid chromatography–tandem mass spectrometry. The developed robust metaproteomics workflow and identification pipeline was used to study the composition and temporal stability of the intestinal metaproteome using faecal samples collected from 3 healthy subjects over a period of six to twelve months. The same samples were also subjected to DNA extraction and analysed for their microbial composition and diversity using the Human Intestinal Tract Chip, a validated phylogenetic microarray. Using metagenome and single genome sequence data out of the thousands of mass spectra generated per sample, approximately 1,000 peptides per sample were identified. Our results indicate that the faecal metaproteome is subject-specific and stable during a one-year period. A stable common core of approximately 1,000 proteins could be recognized in each of the subjects, indicating a common functional core that is mainly involved in carbohydrate transport and degradation. Additionally, a variety of surface proteins could be identified, including potential microbes-host interacting components such as flagellins and pili. Altogether, we observed a highly comparable subject-specific clustering of the metaproteomic and phylogenetic profiles, indicating that the distinct microbial activity is reflected by the individual composition.

Highlights

  • Following birth, our intestinal tract is colonized by an increasingly complex microbial community that is maintained from early to late adulthood [1,2,3]

  • Main characteristics of the metaproteomic pipeline To functionally characterize the intestinal microbiota, we established a metaproteomic pipeline that can be used for rapid analysis of multiple samples (Figure 1)

  • Three fractions per metaproteome separated by using SDS-PAGE were generated and included (i) a high molecular weight metaproteome (HMP) fraction containing proteins larger than 80 kDa, (ii) a low molecular weight metaproteome (LMP) fraction with proteins smaller than 35 kDa, and (iii) a final fraction containing proteins in the range of 35–80 kDa

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Summary

Introduction

Our intestinal tract is colonized by an increasingly complex microbial community that is maintained from early to late adulthood [1,2,3]. The level of sophistication is provided by metagenomic approaches that aim to systematically decode the genetic information of the intestinal microbiota. The number of sequenced single genomes of microbes residing in the human intestine is steadily increasing, with 30,000 new genes having been added recently [11]. These high-throughput analyses lay the groundwork for predicting the genetic potential of the intestinal microbiota. The rapidly increasing catalogue of genes from intestinal origin provides a platform for high-throughput functional characterization [3]

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