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Are commercial providers a viable option for clinical bacterial sequencing?

Bacterial whole-genome sequencing in the clinical setting has the potential to bring major improvements to infection control and clinical practice. Sequencing instruments are not currently available in the majority of routine microbiology laboratories worldwide, but an alternative is to use external...

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Autores principales: Raven, Kathy, Blane, Beth, Churcher, Carol, Parkhill, Julian, Peacock, Sharon J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989584/
https://www.ncbi.nlm.nih.gov/pubmed/29620501
http://dx.doi.org/10.1099/mgen.0.000173
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author Raven, Kathy
Blane, Beth
Churcher, Carol
Parkhill, Julian
Peacock, Sharon J.
author_facet Raven, Kathy
Blane, Beth
Churcher, Carol
Parkhill, Julian
Peacock, Sharon J.
author_sort Raven, Kathy
collection PubMed
description Bacterial whole-genome sequencing in the clinical setting has the potential to bring major improvements to infection control and clinical practice. Sequencing instruments are not currently available in the majority of routine microbiology laboratories worldwide, but an alternative is to use external sequencing providers. To foster discussion around this we investigated whether send-out services were a viable option. Four providers offering MiSeq sequencing were selected based on cost and evaluated based on the service provided and sequence data quality. DNA was prepared from five methicillin-resistant Staphylococcus aureus (MRSA) isolates, four of which were investigated during a previously published outbreak in the UK together with a reference MRSA isolate (ST22 HO 5096 0412). Cost of sequencing per isolate ranged from £155 to £342 and turnaround times from DNA postage to arrival of sequence data ranged from 12 to 63 days. Comparison of commercially generated genomes against the original sequence data demonstrated very high concordance, with no more than one single nucleotide polymorphism (SNP) difference on core genome mapping between the original sequences and the new sequence for all four providers. Multilocus sequence type could not be assigned based on assembly for the two cheapest sequence providers due to fragmented assemblies probably caused by a lower output of sequence data per isolate. Our results indicate that external providers returned highly accurate genome data, but that improvements are required in turnaround time to make this a viable option for use in clinical practice.
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spelling pubmed-59895842018-06-07 Are commercial providers a viable option for clinical bacterial sequencing? Raven, Kathy Blane, Beth Churcher, Carol Parkhill, Julian Peacock, Sharon J. Microb Genom Short Paper Bacterial whole-genome sequencing in the clinical setting has the potential to bring major improvements to infection control and clinical practice. Sequencing instruments are not currently available in the majority of routine microbiology laboratories worldwide, but an alternative is to use external sequencing providers. To foster discussion around this we investigated whether send-out services were a viable option. Four providers offering MiSeq sequencing were selected based on cost and evaluated based on the service provided and sequence data quality. DNA was prepared from five methicillin-resistant Staphylococcus aureus (MRSA) isolates, four of which were investigated during a previously published outbreak in the UK together with a reference MRSA isolate (ST22 HO 5096 0412). Cost of sequencing per isolate ranged from £155 to £342 and turnaround times from DNA postage to arrival of sequence data ranged from 12 to 63 days. Comparison of commercially generated genomes against the original sequence data demonstrated very high concordance, with no more than one single nucleotide polymorphism (SNP) difference on core genome mapping between the original sequences and the new sequence for all four providers. Multilocus sequence type could not be assigned based on assembly for the two cheapest sequence providers due to fragmented assemblies probably caused by a lower output of sequence data per isolate. Our results indicate that external providers returned highly accurate genome data, but that improvements are required in turnaround time to make this a viable option for use in clinical practice. Microbiology Society 2018-04-05 /pmc/articles/PMC5989584/ /pubmed/29620501 http://dx.doi.org/10.1099/mgen.0.000173 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Short Paper
Raven, Kathy
Blane, Beth
Churcher, Carol
Parkhill, Julian
Peacock, Sharon J.
Are commercial providers a viable option for clinical bacterial sequencing?
title Are commercial providers a viable option for clinical bacterial sequencing?
title_full Are commercial providers a viable option for clinical bacterial sequencing?
title_fullStr Are commercial providers a viable option for clinical bacterial sequencing?
title_full_unstemmed Are commercial providers a viable option for clinical bacterial sequencing?
title_short Are commercial providers a viable option for clinical bacterial sequencing?
title_sort are commercial providers a viable option for clinical bacterial sequencing?
topic Short Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989584/
https://www.ncbi.nlm.nih.gov/pubmed/29620501
http://dx.doi.org/10.1099/mgen.0.000173
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