Abstract

Some Eubacterium and Roseburia species are among the most prevalent motile bacteria present in the intestinal microbiota of healthy adults. These flagellate species contribute “cell motility” category genes to the intestinal microbiome and flagellin proteins to the intestinal proteome. We reviewed and revised the annotation of motility genes in the genomes of six Eubacterium and Roseburia species that occur in the human intestinal microbiota and examined their respective locus organization by comparative genomics. Motility gene order was generally conserved across these loci. Five of these species harbored multiple genes for predicted flagellins. Flagellin proteins were isolated from R. inulinivorans strain A2-194 and from E. rectale strains A1-86 and M104/1. The amino-termini sequences of the R. inulinivorans and E. rectale A1-86 proteins were almost identical. These protein preparations stimulated secretion of interleukin-8 (IL-8) from human intestinal epithelial cell lines, suggesting that these flagellins were pro-inflammatory. Flagellins from the other four species were predicted to be pro-inflammatory on the basis of alignment to the consensus sequence of pro-inflammatory flagellins from the β- and γ- proteobacteria. Many fliC genes were deduced to be under the control of σ28. The relative abundance of the target Eubacterium and Roseburia species varied across shotgun metagenomes from 27 elderly individuals. Genes involved in the flagellum biogenesis pathways of these species were variably abundant in these metagenomes, suggesting that the current depth of coverage used for metagenomic sequencing (3.13–4.79 Gb total sequence in our study) insufficiently captures the functional diversity of genomes present at low (≤1%) relative abundance. E. rectale and R. inulinivorans thus appear to synthesize complex flagella composed of flagellin proteins that stimulate IL-8 production. A greater depth of sequencing, improved evenness of sequencing and improved metagenome assembly from short reads will be required to facilitate in silico analyses of complete complex biochemical pathways for low-abundance target species from shotgun metagenomes.

Highlights

  • The mammalian colon is one of the most densely populated microbial ecosystems known [1]

  • We describe the genetic basis for flagellum biogenesis in six of the motile Eubacterium and Roseburia species commonly isolated from the human gastrointestinal (GI) tract

  • While motility may be a colonization factor for enteric Roseburia species [45,46], the expression of flagellin proteins that are recognized by human TLR5 confers a pro-inflammatory capacity upon these species [29]

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Summary

Introduction

The mammalian colon is one of the most densely populated microbial ecosystems known [1]. The microorganisms that occupy this niche, which are collectively known as the colonic microbiota, can influence the health and well-being of the host by affecting physiological and immune functions [2,3,4,5,6,7]. Flagellins and the genes encoding them are variably abundant in the intestines [13,14,15] and the ‘‘cell motility’’ category has been reported as a low-abundance microbial function in this niche [16,17]. Motile bacteria bear significant immunostimulatory potential because humans and other animals harbor cell-surface and cytoplasmic pattern recognition receptors which respond to extra- and intra- cellular flagellin molecules respectively [18,19,20]

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