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Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing

Culture-independent methods that target genome fragments have shown promise in identifying certain pathogens, but the holy grail of comprehensive pathogen genome detection from microbiologically complex samples for subsequent forensic analyses remains a challenge. In the context of an investigation...

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Autores principales: Mu, Andre, Kwong, Jason C., Isles, Nicole S., Gonçalves da Silva, Anders, Schultz, Mark B., Ballard, Susan A., Lane, Courtney R., Carter, Glen P., Williamson, Deborah A., Seemann, Torsten, Stinear, Timothy P., Howden, Benjamin P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336080/
https://www.ncbi.nlm.nih.gov/pubmed/30651402
http://dx.doi.org/10.1128/mSphere.00529-18
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author Mu, Andre
Kwong, Jason C.
Isles, Nicole S.
Gonçalves da Silva, Anders
Schultz, Mark B.
Ballard, Susan A.
Lane, Courtney R.
Carter, Glen P.
Williamson, Deborah A.
Seemann, Torsten
Stinear, Timothy P.
Howden, Benjamin P.
author_facet Mu, Andre
Kwong, Jason C.
Isles, Nicole S.
Gonçalves da Silva, Anders
Schultz, Mark B.
Ballard, Susan A.
Lane, Courtney R.
Carter, Glen P.
Williamson, Deborah A.
Seemann, Torsten
Stinear, Timothy P.
Howden, Benjamin P.
author_sort Mu, Andre
collection PubMed
description Culture-independent methods that target genome fragments have shown promise in identifying certain pathogens, but the holy grail of comprehensive pathogen genome detection from microbiologically complex samples for subsequent forensic analyses remains a challenge. In the context of an investigation of a nosocomial outbreak, we used shotgun metagenomic sequencing of a human fecal sample and a neural network algorithm based on tetranucleotide frequency profiling to reconstruct microbial genomes and tested the same approach using rectal swabs from a second patient. The approach rapidly and readily detected the genome of Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae in the patient fecal specimen and in the rectal swab sample, achieving a level of strain resolution that was sufficient for confident transmission inference during a highly clonal outbreak. The analysis also detected previously unrecognized colonization of the patient by vancomycin-resistant Enterococcus faecium, another multidrug-resistant bacterium. IMPORTANCE The study results reported here perfectly demonstrate the power and promise of clinical metagenomics to recover genome sequences of important drug-resistant bacteria and to rapidly provide rich data that inform outbreak investigations and treatment decisions, independently of the need to culture the organisms.
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spelling pubmed-63360802019-01-25 Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing Mu, Andre Kwong, Jason C. Isles, Nicole S. Gonçalves da Silva, Anders Schultz, Mark B. Ballard, Susan A. Lane, Courtney R. Carter, Glen P. Williamson, Deborah A. Seemann, Torsten Stinear, Timothy P. Howden, Benjamin P. mSphere Research Article Culture-independent methods that target genome fragments have shown promise in identifying certain pathogens, but the holy grail of comprehensive pathogen genome detection from microbiologically complex samples for subsequent forensic analyses remains a challenge. In the context of an investigation of a nosocomial outbreak, we used shotgun metagenomic sequencing of a human fecal sample and a neural network algorithm based on tetranucleotide frequency profiling to reconstruct microbial genomes and tested the same approach using rectal swabs from a second patient. The approach rapidly and readily detected the genome of Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae in the patient fecal specimen and in the rectal swab sample, achieving a level of strain resolution that was sufficient for confident transmission inference during a highly clonal outbreak. The analysis also detected previously unrecognized colonization of the patient by vancomycin-resistant Enterococcus faecium, another multidrug-resistant bacterium. IMPORTANCE The study results reported here perfectly demonstrate the power and promise of clinical metagenomics to recover genome sequences of important drug-resistant bacteria and to rapidly provide rich data that inform outbreak investigations and treatment decisions, independently of the need to culture the organisms. American Society for Microbiology 2019-01-16 /pmc/articles/PMC6336080/ /pubmed/30651402 http://dx.doi.org/10.1128/mSphere.00529-18 Text en Copyright © 2019 Mu et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Mu, Andre
Kwong, Jason C.
Isles, Nicole S.
Gonçalves da Silva, Anders
Schultz, Mark B.
Ballard, Susan A.
Lane, Courtney R.
Carter, Glen P.
Williamson, Deborah A.
Seemann, Torsten
Stinear, Timothy P.
Howden, Benjamin P.
Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing
title Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing
title_full Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing
title_fullStr Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing
title_full_unstemmed Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing
title_short Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing
title_sort reconstruction of the genomes of drug-resistant pathogens for outbreak investigation through metagenomic sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336080/
https://www.ncbi.nlm.nih.gov/pubmed/30651402
http://dx.doi.org/10.1128/mSphere.00529-18
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