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Candidatus Mycoplasma girerdii replicates, diversifies, and co-occurs with Trichomonas vaginalis in the oral cavity of a premature infant
Journal article   Open access   Peer reviewed

Candidatus Mycoplasma girerdii replicates, diversifies, and co-occurs with Trichomonas vaginalis in the oral cavity of a premature infant

Elizabeth K Costello, Christine L Sun, Erica M Carlisle, Michael J Morowitz, Jillian F Banfield and David A Relman
Scientific reports, Vol.7(1), 3764
06/19/2017
DOI: 10.1038/s41598-017-03821-7
PMCID: PMC5476646
PMID: 28630471
url
https://doi.org/10.1038/s41598-017-03821-7View
Published (Version of record) Open Access

Abstract

Genital mycoplasmas, which can be vertically transmitted, have been implicated in preterm birth, neonatal infections, and chronic lung disease of prematurity. Our prior work uncovered 16S rRNA genes belonging to a novel, as-yet-uncultivated mycoplasma (lineage 'Mnola') in the oral cavity of a premature neonate. Here, we characterize the organism's associated community, growth status, metabolic potential, and population diversity. Sequencing of genomic DNA from the infant's saliva yielded 1.44 Gbp of high-quality, non-human read data, from which we recovered three essentially complete (including 'Mnola') and three partial draft genomes (including Trichomonas vaginalis). The completed 629,409-bp 'Mnola' genome (Candidatus Mycoplasma girerdii str. UC-B3) was distinct at the strain level from its closest relative, vaginally-derived Ca. M. girerdii str. VCU-M1, which is also associated with T. vaginalis. Replication rate measurements indicated growth of str. UC-B3 within the infant. Genes encoding surface-associated proteins and restriction-modification systems were especially diverse within and between strains. In UC-B3, the population genetic underpinnings of phase variable expression were evident in vivo. Unique among mycoplasmas, Ca. M. girerdii encodes pyruvate-ferredoxin oxidoreductase and may be sensitive to metronidazole. This study reveals a metabolically unique mycoplasma colonizing a premature neonate, and establishes the value of genome-resolved metagenomics in tracking phase variation.
Mycoplasma Infections - pathology Mycoplasma Infections - microbiology Humans Mycoplasma - genetics Male Trichomonas vaginalis - genetics Mycoplasma Infections - genetics Trichomonas Infections - microbiology Mouth - microbiology Trichomonas Infections - metabolism Trichomonas Infections - pathology Mycoplasma Infections - metabolism Mycoplasma - growth & development Mouth - pathology Trichomonas vaginalis - growth & development Female Trichomonas Infections - genetics Infant, Newborn

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