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The complete genome sequence of unculturable Mycoplasma faucium obtained through clinical metagenomic next-generation sequencing.
Sabat, Artur J; Durfee, Tim; Baldwin, Schuyler; Akkerboom, Viktoria; Voss, Andreas; Friedrich, Alexander W; Bathoorn, Erik.
Afiliación
  • Sabat AJ; Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Durfee T; DNASTAR, Inc., Madison, WI, United States.
  • Baldwin S; DNASTAR, Inc., Madison, WI, United States.
  • Akkerboom V; Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Voss A; Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • Friedrich AW; University Hospital Münster, University of Münster, Münster, Germany.
  • Bathoorn E; Department of Medical Microbiology and Infection Prevention, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Front Cell Infect Microbiol ; 14: 1368923, 2024.
Article en En | MEDLINE | ID: mdl-38694516
ABSTRACT

Introduction:

Diagnosing Mycoplasma faucium poses challenges, and it's unclear if its rare isolation is due to infrequent occurrence or its fastidious nutritional requirements.

Methods:

This study analyzes the complete genome sequence of M. faucium, obtained directly from the pus of a sternum infection in a lung transplant patient using metagenomic sequencing.

Results:

Genome analysis revealed limited therapeutic options for the M. faucium infection, primarily susceptibility to tetracyclines. Three classes of mobile genetic elements were identified two new insertion sequences, a new prophage (phiUMCG-1), and a species-specific variant of a mycoplasma integrative and conjugative element (MICE). Additionally, a Type I Restriction-Modification system was identified, featuring 5'-terminally truncated hsdS pseudogenes with overlapping repeats, indicating the potential for forming alternative hsdS variants through recombination.

Conclusion:

This study represents the first-ever acquisition of a complete circularized bacterial genome directly from a patient sample obtained from invasive infection of a primary sterile site using culture-independent, PCR-free clinical metagenomics.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma Bacteriano / Metagenómica / Secuenciación de Nucleótidos de Alto Rendimiento / Mycoplasma Límite: Humans Idioma: En Revista: Front Cell Infect Microbiol Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma Bacteriano / Metagenómica / Secuenciación de Nucleótidos de Alto Rendimiento / Mycoplasma Límite: Humans Idioma: En Revista: Front Cell Infect Microbiol Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos