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Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013

BACKGROUND: Mandatory reporting of methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infections (BSI) has occurred in England for over 15years. Epidemiological information is recorded, but routine collection of isolates for characterisation has not been routinely undertaken. Ongoing dev...

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Autores principales: Toleman, Michelle S, Reuter, Sandra, Jamrozy, Dorota, Wilson, Hayley J, Blane, Beth, Harrison, Ewan M, Coll, Francesc, Hope, Russell J, Kearns, Angela, Parkhill, Julian, Peacock, Sharon J, Török, M Estée
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Centre for Disease Prevention and Control (ECDC) 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351993/
https://www.ncbi.nlm.nih.gov/pubmed/30696529
http://dx.doi.org/10.2807/1560-7917.ES.2019.24.4.1800215
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author Toleman, Michelle S
Reuter, Sandra
Jamrozy, Dorota
Wilson, Hayley J
Blane, Beth
Harrison, Ewan M
Coll, Francesc
Hope, Russell J
Kearns, Angela
Parkhill, Julian
Peacock, Sharon J
Török, M Estée
author_facet Toleman, Michelle S
Reuter, Sandra
Jamrozy, Dorota
Wilson, Hayley J
Blane, Beth
Harrison, Ewan M
Coll, Francesc
Hope, Russell J
Kearns, Angela
Parkhill, Julian
Peacock, Sharon J
Török, M Estée
author_sort Toleman, Michelle S
collection PubMed
description BACKGROUND: Mandatory reporting of methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infections (BSI) has occurred in England for over 15years. Epidemiological information is recorded, but routine collection of isolates for characterisation has not been routinely undertaken. Ongoing developments in whole-genome sequencing (WGS) have demonstrated its value in outbreak investigations and for determining the spread of antimicrobial resistance and bacterial population structure. Benefits of adding genomics to routine epidemiological MRSA surveillance are unknown. AIM: To determine feasibility and potential utility of adding genomics to epidemiological surveillance of MRSA. METHODS: We conducted an epidemiological and genomic survey of MRSA BSI in England over a 1-year period (1 October 2012­–30 September 2013). RESULTS: During the study period, 903 cases of MRSA BSI were reported; 425 isolates were available for sequencing of which, 276 (65%) were clonal complex (CC) 22. Addition of 64 MRSA genomes from published outbreak investigations showed that the study genomes could provide context for outbreak isolates and supported cluster identification. Comparison to other MRSA genome collections demonstrated variation in clonal diversity achieved through different sampling strategies and identified potentially high-risk clones e.g. USA300 and local expansion of CC5 MRSA in South West England. CONCLUSIONS: We demonstrate the potential utility of combined epidemiological and genomic MRSA BSI surveillance to determine the national population structure of MRSA, contextualise previous MRSA outbreaks, and detect potentially high-risk lineages. These findings support the integration of epidemiological and genomic surveillance for MRSA BSI as a step towards a comprehensive surveillance programme in England.
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spelling pubmed-63519932019-02-15 Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013 Toleman, Michelle S Reuter, Sandra Jamrozy, Dorota Wilson, Hayley J Blane, Beth Harrison, Ewan M Coll, Francesc Hope, Russell J Kearns, Angela Parkhill, Julian Peacock, Sharon J Török, M Estée Euro Surveill Research BACKGROUND: Mandatory reporting of methicillin-resistant Staphylococcus aureus (MRSA) bloodstream infections (BSI) has occurred in England for over 15years. Epidemiological information is recorded, but routine collection of isolates for characterisation has not been routinely undertaken. Ongoing developments in whole-genome sequencing (WGS) have demonstrated its value in outbreak investigations and for determining the spread of antimicrobial resistance and bacterial population structure. Benefits of adding genomics to routine epidemiological MRSA surveillance are unknown. AIM: To determine feasibility and potential utility of adding genomics to epidemiological surveillance of MRSA. METHODS: We conducted an epidemiological and genomic survey of MRSA BSI in England over a 1-year period (1 October 2012­–30 September 2013). RESULTS: During the study period, 903 cases of MRSA BSI were reported; 425 isolates were available for sequencing of which, 276 (65%) were clonal complex (CC) 22. Addition of 64 MRSA genomes from published outbreak investigations showed that the study genomes could provide context for outbreak isolates and supported cluster identification. Comparison to other MRSA genome collections demonstrated variation in clonal diversity achieved through different sampling strategies and identified potentially high-risk clones e.g. USA300 and local expansion of CC5 MRSA in South West England. CONCLUSIONS: We demonstrate the potential utility of combined epidemiological and genomic MRSA BSI surveillance to determine the national population structure of MRSA, contextualise previous MRSA outbreaks, and detect potentially high-risk lineages. These findings support the integration of epidemiological and genomic surveillance for MRSA BSI as a step towards a comprehensive surveillance programme in England. European Centre for Disease Prevention and Control (ECDC) 2019-01-24 /pmc/articles/PMC6351993/ /pubmed/30696529 http://dx.doi.org/10.2807/1560-7917.ES.2019.24.4.1800215 Text en This article is copyright of the authors or their affiliated institutions, 2019. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.
spellingShingle Research
Toleman, Michelle S
Reuter, Sandra
Jamrozy, Dorota
Wilson, Hayley J
Blane, Beth
Harrison, Ewan M
Coll, Francesc
Hope, Russell J
Kearns, Angela
Parkhill, Julian
Peacock, Sharon J
Török, M Estée
Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013
title Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013
title_full Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013
title_fullStr Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013
title_full_unstemmed Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013
title_short Prospective genomic surveillance of methicillin-resistant Staphylococcus aureus (MRSA) associated with bloodstream infection, England, 1 October 2012 to 30 September 2013
title_sort prospective genomic surveillance of methicillin-resistant staphylococcus aureus (mrsa) associated with bloodstream infection, england, 1 october 2012 to 30 september 2013
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351993/
https://www.ncbi.nlm.nih.gov/pubmed/30696529
http://dx.doi.org/10.2807/1560-7917.ES.2019.24.4.1800215
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