A multicentre outbreak of ST45 MRSA containing deletions in the spa gene in New South Wales, Australia.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 05 2020
Historique:
received: 30 10 2019
revised: 01 12 2019
accepted: 16 12 2019
pubmed: 6 2 2020
medline: 25 6 2021
entrez: 5 2 2020
Statut: ppublish

Résumé

Early identification of MRSA by diagnostic medical microbiology laboratories enables improved antimicrobial choice and outcomes. The Cepheid Xpert® MRSA/SA BC test rapidly identifies Staphylococcus aureus bloodstream infections through spa gene detection and methicillin resistance via mecA gene detection. Recent emergence of S. aureus with deletions in the spa gene has resulted in false-negative results for this test, leading to misidentification of infections with this organism, particularly MRSA ST45. To investigate the emergence and prevalence of ST45 MRSA in New South Wales (NSW), Australia. WGS read data from six NSW hospitals were collected for 131 ST45 MRSA isolates and analysed. Of the 131 ST45 MRSA investigated, 88.5% (116/131) contained a deletion in the spa gene that appeared to have arisen once in approximately 2010 followed by clonal expansion. Given the successful establishment of this 'spa-deletion' MRSA clone, the Cepheid Xpert® MRSA/SA BC test became unreliable for confirming S. aureus bacteraemia in NSW. Subsequently, the algorithm used by this test has been updated and evaluated to take into account the presence of S. aureus with either a spa deletion or SCCmec target variations. This study highlighted the applied use of WGS for assessing diagnostic assays and informing necessary changes to ensure the viability of the Cepheid Xpert® MRSA/SA BC test in the context of the new 'spa-deletion' MRSA clone. It demonstrated how continued surveillance through WGS can reveal evolutionary events that may impact diagnostic assays, allowing corrective modifications to be made in real time.

Sections du résumé

BACKGROUND
Early identification of MRSA by diagnostic medical microbiology laboratories enables improved antimicrobial choice and outcomes. The Cepheid Xpert® MRSA/SA BC test rapidly identifies Staphylococcus aureus bloodstream infections through spa gene detection and methicillin resistance via mecA gene detection. Recent emergence of S. aureus with deletions in the spa gene has resulted in false-negative results for this test, leading to misidentification of infections with this organism, particularly MRSA ST45.
OBJECTIVES
To investigate the emergence and prevalence of ST45 MRSA in New South Wales (NSW), Australia.
METHODS
WGS read data from six NSW hospitals were collected for 131 ST45 MRSA isolates and analysed.
RESULTS
Of the 131 ST45 MRSA investigated, 88.5% (116/131) contained a deletion in the spa gene that appeared to have arisen once in approximately 2010 followed by clonal expansion. Given the successful establishment of this 'spa-deletion' MRSA clone, the Cepheid Xpert® MRSA/SA BC test became unreliable for confirming S. aureus bacteraemia in NSW. Subsequently, the algorithm used by this test has been updated and evaluated to take into account the presence of S. aureus with either a spa deletion or SCCmec target variations.
CONCLUSIONS
This study highlighted the applied use of WGS for assessing diagnostic assays and informing necessary changes to ensure the viability of the Cepheid Xpert® MRSA/SA BC test in the context of the new 'spa-deletion' MRSA clone. It demonstrated how continued surveillance through WGS can reveal evolutionary events that may impact diagnostic assays, allowing corrective modifications to be made in real time.

Identifiants

pubmed: 32016400
pii: 5722229
doi: 10.1093/jac/dkz560
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1112-1116

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Alicia G Beukers (AG)

NSW Health Pathology, Department of Infectious Diseases and Microbiology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

Peter Newton (P)

NSW Health Pathology, Microbiology, Wollongong Hospital, Wollongong, NSW, Australia.

Bernard Hudson (B)

NSW Health Pathology, Microbiology and Infectious Diseases, Royal North Shore Private Hospital, St Leonards, NSW, Australia.

Kimberly Ross (K)

NSW Health Pathology, Microbiology, John Hunter Hospital, New Lambton Heights, NSW, Australia.

Thomas Gottlieb (T)

NSW Health Pathology, Department of Microbiology and Infectious Diseases, Concord Hospital, Concord, NSW, Australia.

Matthew O'Sullivan (M)

NSW Health Pathology, Microbiology Department, Westmead Hospital, Westmead, NSW, Australia.

Denise A Daley (DA)

Australian Group on Antimicrobial Resistance, Perth, WA, Australia.

Stanley Pang (S)

Australian Group on Antimicrobial Resistance, Perth, WA, Australia.
Antimicrobial Resistance and Infectious Diseases Research Laboratory, Murdoch University, Murdoch, WA, Australia.

Geoffrey W Coombs (GW)

Australian Group on Antimicrobial Resistance, Perth, WA, Australia.
Antimicrobial Resistance and Infectious Diseases Research Laboratory, Murdoch University, Murdoch, WA, Australia.

Sebastiaan J van Hal (SJ)

NSW Health Pathology, Department of Infectious Diseases and Microbiology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.

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