Journal article
Candidatus Mycoplasma girerdii replicates, diversifies, and co-occurs with Trichomonas vaginalis in the oral cavity of a premature infant
Scientific reports, Vol.7(1), 3764
06/19/2017
DOI: 10.1038/s41598-017-03821-7
PMCID: PMC5476646
PMID: 28630471
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.
Details
- Title: Subtitle
- Candidatus Mycoplasma girerdii replicates, diversifies, and co-occurs with Trichomonas vaginalis in the oral cavity of a premature infant
- Creators
- Elizabeth K Costello - Department of Medicine, Division of Infectious Diseases, Stanford University School of Medicine, Stanford, CA, 94305, USAChristine L Sun - Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, 94305, USAErica M Carlisle - Department of Surgery, Division of Pediatric Surgery, University of Iowa College of Medicine, Iowa City, IA, 52242, USAMichael J Morowitz - Department of Surgery, Division of Pediatric Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15224, USAJillian F Banfield - Department of Earth & Planetary Science, University of California, Berkeley, CA, 94720, USADavid A Relman - Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, 94304, USA. relman@stanford.edu
- Resource Type
- Journal article
- Publication Details
- Scientific reports, Vol.7(1), 3764
- DOI
- 10.1038/s41598-017-03821-7
- PMID
- 28630471
- PMCID
- PMC5476646
- NLM abbreviation
- Sci Rep
- ISSN
- 2045-2322
- eISSN
- 2045-2322
- Publisher
- England
- Grant note
- K99 HD074743 / NICHD NIH HHS R01 AI092531 / NIAID NIH HHS
- Language
- English
- Date published
- 06/19/2017
- Academic Unit
- Stead Family Department of Pediatrics; Surgery
- Record Identifier
- 9984051769902771
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