Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing

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Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing. / Bartels, M D; Larner-Svensson, H; Meiniche, H; Kristoffersen, K; Schonning, K; Nielsen, J B; Rohde, S M; Christensen, L B; Skibsted, A W; Jarlov, J O; Johansen, H K; Andersen, L P; Petersen, I S; Crook, D W; Bowden, R; Boye, K; Worning, P; Westh, H.

I: Eurosurveillance, Bind 20, Nr. 17, 21112, 30.04.2015.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bartels, MD, Larner-Svensson, H, Meiniche, H, Kristoffersen, K, Schonning, K, Nielsen, JB, Rohde, SM, Christensen, LB, Skibsted, AW, Jarlov, JO, Johansen, HK, Andersen, LP, Petersen, IS, Crook, DW, Bowden, R, Boye, K, Worning, P & Westh, H 2015, 'Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing', Eurosurveillance, bind 20, nr. 17, 21112. <http://www.eurosurveillance.org/ViewArticle.aspx?ArticleId=21112>

APA

Bartels, M. D., Larner-Svensson, H., Meiniche, H., Kristoffersen, K., Schonning, K., Nielsen, J. B., Rohde, S. M., Christensen, L. B., Skibsted, A. W., Jarlov, J. O., Johansen, H. K., Andersen, L. P., Petersen, I. S., Crook, D. W., Bowden, R., Boye, K., Worning, P., & Westh, H. (2015). Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing. Eurosurveillance, 20(17), [21112]. http://www.eurosurveillance.org/ViewArticle.aspx?ArticleId=21112

Vancouver

Bartels MD, Larner-Svensson H, Meiniche H, Kristoffersen K, Schonning K, Nielsen JB o.a. Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing. Eurosurveillance. 2015 apr. 30;20(17). 21112.

Author

Bartels, M D ; Larner-Svensson, H ; Meiniche, H ; Kristoffersen, K ; Schonning, K ; Nielsen, J B ; Rohde, S M ; Christensen, L B ; Skibsted, A W ; Jarlov, J O ; Johansen, H K ; Andersen, L P ; Petersen, I S ; Crook, D W ; Bowden, R ; Boye, K ; Worning, P ; Westh, H. / Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing. I: Eurosurveillance. 2015 ; Bind 20, Nr. 17.

Bibtex

@article{69c3c36d74d04ed3bed2ef2033b89527,
title = "Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing",
abstract = "Typing of meticillin resistant Staphylococcus aureus (MRSA) by whole genome sequencing (WGS) is performed routinely in Copenhagen since January 2013. We describe the relatedness, based on WGS data and epidemiological data, of 341 MRSA isolates. These comprised all MRSA (n = 300) identified in Copenhagen in the first five months of 2013. Moreover, because MRSA of staphylococcal protein A (spa)-type 304 (t304), sequence type (ST) 6 had been associated with a continuous neonatal ward outbreak in Copenhagen starting in 2011, 41 t304 isolates collected in the city between 2010 and 2012 were also included. Isolates from 2013 found to be of t304, ST6 (n=14) were compared to the 41 earlier isolates. In the study, isolates of clonal complex (CC) 22 were examined in detail, as this CC has been shown to include the hospital-acquired epidemic MRSA (EMRSA-15) clone. Finally, all MRSA ST80 were also further analysed, as representatives of an important community-acquired MRSA in Europe. Overall the analysis identified 85 spa-types and 35 STs from 17 CCs. WGS confirmed the relatedness of epidemiologically linked t304 neonatal outbreak isolates. Several non-outbreak related patients had isolates closely related to the neonatal isolates suggesting unrecognised community chains of transmission and insufficient epidemiological data. Only four CC22 isolates were related to EMRSA-15. No community spread was observed among the 13 ST80 isolates. WGS successfully replaced conventional typing and added information to epidemiological surveillance. Creation of a MRSA database allows clustering of isolates based on single nucleotide polymorphism (SNP) calling and has improved our understanding of MRSA transmission.",
keywords = "Bacterial Toxins, Denmark, Exotoxins, Genome, Bacterial, Humans, Leukocidins, Methicillin-Resistant Staphylococcus aureus, Molecular Epidemiology, Molecular Typing, Polymorphism, Single Nucleotide, Sequence Analysis, DNA, Staphylococcal Infections, Staphylococcal Protein A",
author = "Bartels, {M D} and H Larner-Svensson and H Meiniche and K Kristoffersen and K Schonning and Nielsen, {J B} and Rohde, {S M} and Christensen, {L B} and Skibsted, {A W} and Jarlov, {J O} and Johansen, {H K} and Andersen, {L P} and Petersen, {I S} and Crook, {D W} and R Bowden and K Boye and P Worning and H Westh",
year = "2015",
month = apr,
day = "30",
language = "English",
volume = "20",
journal = "Eurosurveillance",
issn = "1025-496X",
publisher = "Centre Europeen pour la Surveillance Epidemiologique du SIDA",
number = "17",

}

RIS

TY - JOUR

T1 - Monitoring meticillin resistant Staphylococcus aureus and its spread in Copenhagen, Denmark, 2013, through routine whole genome sequencing

AU - Bartels, M D

AU - Larner-Svensson, H

AU - Meiniche, H

AU - Kristoffersen, K

AU - Schonning, K

AU - Nielsen, J B

AU - Rohde, S M

AU - Christensen, L B

AU - Skibsted, A W

AU - Jarlov, J O

AU - Johansen, H K

AU - Andersen, L P

AU - Petersen, I S

AU - Crook, D W

AU - Bowden, R

AU - Boye, K

AU - Worning, P

AU - Westh, H

PY - 2015/4/30

Y1 - 2015/4/30

N2 - Typing of meticillin resistant Staphylococcus aureus (MRSA) by whole genome sequencing (WGS) is performed routinely in Copenhagen since January 2013. We describe the relatedness, based on WGS data and epidemiological data, of 341 MRSA isolates. These comprised all MRSA (n = 300) identified in Copenhagen in the first five months of 2013. Moreover, because MRSA of staphylococcal protein A (spa)-type 304 (t304), sequence type (ST) 6 had been associated with a continuous neonatal ward outbreak in Copenhagen starting in 2011, 41 t304 isolates collected in the city between 2010 and 2012 were also included. Isolates from 2013 found to be of t304, ST6 (n=14) were compared to the 41 earlier isolates. In the study, isolates of clonal complex (CC) 22 were examined in detail, as this CC has been shown to include the hospital-acquired epidemic MRSA (EMRSA-15) clone. Finally, all MRSA ST80 were also further analysed, as representatives of an important community-acquired MRSA in Europe. Overall the analysis identified 85 spa-types and 35 STs from 17 CCs. WGS confirmed the relatedness of epidemiologically linked t304 neonatal outbreak isolates. Several non-outbreak related patients had isolates closely related to the neonatal isolates suggesting unrecognised community chains of transmission and insufficient epidemiological data. Only four CC22 isolates were related to EMRSA-15. No community spread was observed among the 13 ST80 isolates. WGS successfully replaced conventional typing and added information to epidemiological surveillance. Creation of a MRSA database allows clustering of isolates based on single nucleotide polymorphism (SNP) calling and has improved our understanding of MRSA transmission.

AB - Typing of meticillin resistant Staphylococcus aureus (MRSA) by whole genome sequencing (WGS) is performed routinely in Copenhagen since January 2013. We describe the relatedness, based on WGS data and epidemiological data, of 341 MRSA isolates. These comprised all MRSA (n = 300) identified in Copenhagen in the first five months of 2013. Moreover, because MRSA of staphylococcal protein A (spa)-type 304 (t304), sequence type (ST) 6 had been associated with a continuous neonatal ward outbreak in Copenhagen starting in 2011, 41 t304 isolates collected in the city between 2010 and 2012 were also included. Isolates from 2013 found to be of t304, ST6 (n=14) were compared to the 41 earlier isolates. In the study, isolates of clonal complex (CC) 22 were examined in detail, as this CC has been shown to include the hospital-acquired epidemic MRSA (EMRSA-15) clone. Finally, all MRSA ST80 were also further analysed, as representatives of an important community-acquired MRSA in Europe. Overall the analysis identified 85 spa-types and 35 STs from 17 CCs. WGS confirmed the relatedness of epidemiologically linked t304 neonatal outbreak isolates. Several non-outbreak related patients had isolates closely related to the neonatal isolates suggesting unrecognised community chains of transmission and insufficient epidemiological data. Only four CC22 isolates were related to EMRSA-15. No community spread was observed among the 13 ST80 isolates. WGS successfully replaced conventional typing and added information to epidemiological surveillance. Creation of a MRSA database allows clustering of isolates based on single nucleotide polymorphism (SNP) calling and has improved our understanding of MRSA transmission.

KW - Bacterial Toxins

KW - Denmark

KW - Exotoxins

KW - Genome, Bacterial

KW - Humans

KW - Leukocidins

KW - Methicillin-Resistant Staphylococcus aureus

KW - Molecular Epidemiology

KW - Molecular Typing

KW - Polymorphism, Single Nucleotide

KW - Sequence Analysis, DNA

KW - Staphylococcal Infections

KW - Staphylococcal Protein A

M3 - Journal article

C2 - 25955776

VL - 20

JO - Eurosurveillance

JF - Eurosurveillance

SN - 1025-496X

IS - 17

M1 - 21112

ER -

ID: 160404406