TY - JOUR
T1 - The complete genome sequence of unculturable Mycoplasma faucium obtained through clinical metagenomic next-generation sequencing
AU - Sabat, Artur J.
AU - Durfee, Tim
AU - Baldwin, Schuyler
AU - Akkerboom, Viktoria
AU - Voss, Andreas
AU - Friedrich, Alexander W.
AU - Bathoorn, Erik
N1 - Publisher Copyright:
Copyright © 2024 Sabat, Durfee, Baldwin, Akkerboom, Voss, Friedrich and Bathoorn.
PY - 2024/4/16
Y1 - 2024/4/16
N2 - 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.
AB - 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.
KW - ice
KW - insertion sequence
KW - lung transplant patient
KW - metagenomics
KW - Mycoplasma faucium
UR - http://www.scopus.com/inward/record.url?scp=85191796827&partnerID=8YFLogxK
U2 - 10.3389/fcimb.2024.1368923
DO - 10.3389/fcimb.2024.1368923
M3 - Article
C2 - 38694516
AN - SCOPUS:85191796827
SN - 2235-2988
VL - 14
JO - Frontiers in Cellular and Infection Microbiology
JF - Frontiers in Cellular and Infection Microbiology
M1 - 1368923
ER -