Abstract

Mycoplasma hominis is an opportunistic human mycoplasma. Two other pathogenic human species, M. genitalium and Ureaplasma parvum, reside within the same natural niche as M. hominis: the urogenital tract. These three species have overlapping, but distinct, pathogenic roles. They have minimal genomes and, thus, reduced metabolic capabilities characterized by distinct energy-generating pathways. Analysis of the M. hominis PG21 genome sequence revealed that it is the second smallest genome among self-replicating free living organisms (665,445 bp, 537 coding sequences (CDSs)). Five clusters of genes were predicted to have undergone horizontal gene transfer (HGT) between M. hominis and the phylogenetically distant U. parvum species. We reconstructed M. hominis metabolic pathways from the predicted genes, with particular emphasis on energy-generating pathways. The Embden–Meyerhoff–Parnas pathway was incomplete, with a single enzyme absent. We identified the three proteins constituting the arginine dihydrolase pathway. This pathway was found essential to promote growth in vivo. The predicted presence of dimethylarginine dimethylaminohydrolase suggested that arginine catabolism is more complex than initially described. This enzyme may have been acquired by HGT from non-mollicute bacteria. Comparison of the three minimal mollicute genomes showed that 247 CDSs were common to all three genomes, whereas 220 CDSs were specific to M. hominis, 172 CDSs were specific to M. genitalium, and 280 CDSs were specific to U. parvum. Within these species-specific genes, two major sets of genes could be identified: one including genes involved in various energy-generating pathways, depending on the energy source used (glucose, urea, or arginine) and another involved in cytadherence and virulence. Therefore, a minimal mycoplasma cell, not including cytadherence and virulence-related genes, could be envisaged containing a core genome (247 genes), plus a set of genes required for providing energy. For M. hominis, this set would include 247+9 genes, resulting in a theoretical minimal genome of 256 genes.

Highlights

  • Mycoplasma hominis is an opportunistic human mycoplasma species which resides, as a commensal, in the lower urogenital tract

  • Our findings suggest that M. hominis and U. parvum underwent genetic exchange, probably while sharing a common host

  • For M. hominis, this minimal genome, not including cytadherence and virulence-related genes, can be defined comprising the 247 genes shared by the three minimal genital mollicutes, combined with a set of nine genes needed for energy production for cell metabolism

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Summary

Introduction

Mycoplasma hominis is an opportunistic human mycoplasma species which resides, as a commensal, in the lower urogenital tract It can cause pelvic inflammatory disease and postpartum or postabortion fevers, and has been associated with bacterial vaginosis [1]. M. genitalium is the only mycoplasmal species involved in cervicitis, whereas Ureaplasma spp. are significantly associated with prematurity, low birth weight and chronic lung disease in infants [1]. These three urogenital species belong to two different phylogenetic groups within the class Mollicutes: M. genitalium and Ureaplasma spp. belong to the Pneumoniae group and M. hominis belongs to the Hominis group. More recent studies have attempted to reconstruct its genome by chemical synthesis [7,8], with a view

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