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Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes

OBJECTIVES: Genome sequencing will be increasingly used in the clinical setting to tailor antimicrobial prescribing and inform infection control outbreaks. A recent technological innovation that could reduce the delay between pathogen sampling and data generation is single molecule sequencing. An ex...

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Autores principales: Judge, Kim, Harris, Simon R., Reuter, Sandra, Parkhill, Julian, Peacock, Sharon J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566964/
https://www.ncbi.nlm.nih.gov/pubmed/26221019
http://dx.doi.org/10.1093/jac/dkv206
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author Judge, Kim
Harris, Simon R.
Reuter, Sandra
Parkhill, Julian
Peacock, Sharon J.
author_facet Judge, Kim
Harris, Simon R.
Reuter, Sandra
Parkhill, Julian
Peacock, Sharon J.
author_sort Judge, Kim
collection PubMed
description OBJECTIVES: Genome sequencing will be increasingly used in the clinical setting to tailor antimicrobial prescribing and inform infection control outbreaks. A recent technological innovation that could reduce the delay between pathogen sampling and data generation is single molecule sequencing. An example of this technology, which is undergoing evaluation through an early access programme, is the Oxford Nanopore MinION. METHODS: We undertook a feasibility study on six clinically significant pathogens, comparing the MinION to the Illumina MiSeq and PacBio RSII platforms. Genomic DNA was prepared and sequenced using the MinION as instructed by the manufacturer, and Illumina MiSeq and PacBio sequencing was performed using established methods. RESULTS: An evaluation of the accuracy of the MinION based on sequencing of an MRSA isolate showed that error rates were higher in the MinION reads, but provided an even coverage across the entire genome length. The MinION detected all of the expected carbapenemases and ESBL genes in five Gram-negative isolates and the mecA gene in an MRSA isolate. CONCLUSIONS: The MinION can detect the presence of acquired resistance genes, but improvements in accuracy are needed so that antimicrobial resistance associated with mutations in chromosomal genes can be identified.
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spelling pubmed-45669642015-09-15 Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes Judge, Kim Harris, Simon R. Reuter, Sandra Parkhill, Julian Peacock, Sharon J. J Antimicrob Chemother Original Research OBJECTIVES: Genome sequencing will be increasingly used in the clinical setting to tailor antimicrobial prescribing and inform infection control outbreaks. A recent technological innovation that could reduce the delay between pathogen sampling and data generation is single molecule sequencing. An example of this technology, which is undergoing evaluation through an early access programme, is the Oxford Nanopore MinION. METHODS: We undertook a feasibility study on six clinically significant pathogens, comparing the MinION to the Illumina MiSeq and PacBio RSII platforms. Genomic DNA was prepared and sequenced using the MinION as instructed by the manufacturer, and Illumina MiSeq and PacBio sequencing was performed using established methods. RESULTS: An evaluation of the accuracy of the MinION based on sequencing of an MRSA isolate showed that error rates were higher in the MinION reads, but provided an even coverage across the entire genome length. The MinION detected all of the expected carbapenemases and ESBL genes in five Gram-negative isolates and the mecA gene in an MRSA isolate. CONCLUSIONS: The MinION can detect the presence of acquired resistance genes, but improvements in accuracy are needed so that antimicrobial resistance associated with mutations in chromosomal genes can be identified. Oxford University Press 2015-10 2015-07-28 /pmc/articles/PMC4566964/ /pubmed/26221019 http://dx.doi.org/10.1093/jac/dkv206 Text en © The Author 2015. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Judge, Kim
Harris, Simon R.
Reuter, Sandra
Parkhill, Julian
Peacock, Sharon J.
Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes
title Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes
title_full Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes
title_fullStr Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes
title_full_unstemmed Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes
title_short Early insights into the potential of the Oxford Nanopore MinION for the detection of antimicrobial resistance genes
title_sort early insights into the potential of the oxford nanopore minion for the detection of antimicrobial resistance genes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566964/
https://www.ncbi.nlm.nih.gov/pubmed/26221019
http://dx.doi.org/10.1093/jac/dkv206
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