4.5 Article

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

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EUROSURVEILLANCE
卷 24, 期 4, 页码 42-53

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EUR CENTRE DIS PREVENTION & CONTROL
DOI: 10.2807/1560-7917.ES.2019.24.4.1800215

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资金

  1. UK Clinical Research Collaboration Translational Infection Research Initiative
  2. Medical Research Council [G1000803]
  3. Biotechnology and Biological Sciences Research Council
  4. National Institute for Health Research on behalf of the Department of Health
  5. Chief Scientist Office of the Scottish Government Health Directorate
  6. Wellcome Trust [098051, 201344/Z/16/Z]
  7. Academy of Medical Sciences
  8. Health Foundation
  9. National Institute for Health Research Cambridge Biomedical Research Centre
  10. MRC [G1000803, MR/S00291X/1, MR/N029399/1] Funding Source: UKRI
  11. Wellcome Trust [201344/Z/16/Z] Funding Source: Wellcome Trust

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Background: Mandatory reporting of meticillin-resistant Staphylococcus aureus (MRSA) bloodstream infections (BSI) has occurred in England for over 15 years. 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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