Journal article
Whole-genome sequencing shows that patient-to-patient transmission rarely accounts for acquisition of Staphylococcus aureus in an intensive care unit.
- Abstract:
- BACKGROUND: Strategies to prevent Staphylococcus aureus infection in hospitals focus on patient-to-patient transmission. We used whole-genome sequencing to investigate the role of colonized patients as the source of new S. aureus acquisitions, and the reliability of identifying patient-to-patient transmission using the conventional approach of spa typing and overlapping patient stay. METHODS: Over 14 months, all unselected patients admitted to an adult intensive care unit (ICU) were serially screened for S. aureus. All available isolates (n = 275) were spa typed and underwent whole-genome sequencing to investigate their relatedness at high resolution. RESULTS: Staphylococcus aureus was carried by 185 of 1109 patients sampled within 24 hours of ICU admission (16.7%); 59 (5.3%) patients carried methicillin-resistant S. aureus (MRSA). Forty-four S. aureus (22 MRSA) acquisitions while on ICU were detected. Isolates were available for genetic analysis from 37 acquisitions. Whole-genome sequencing indicated that 7 of these 37 (18.9%) were transmissions from other colonized patients. Conventional methods (spa typing combined with overlapping patient stay) falsely identified 3 patient-to-patient transmissions (all MRSA) and failed to detect 2 acquisitions and 4 transmissions (2 MRSA). CONCLUSIONS: Only a minority of S. aureus acquisitions can be explained by patient-to-patient transmission. Whole-genome sequencing provides the resolution to disprove transmission events indicated by conventional methods and also to reveal otherwise unsuspected transmission events. Whole-genome sequencing should replace conventional methods for detection of nosocomial S. aureus transmission.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 751.1KB, Terms of use)
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- Publisher copy:
- 10.1093/cid/cit807
Authors
- Publisher:
- Oxford University Press
- Journal:
- Clinical infectious diseases : an official publication of the Infectious Diseases Society of America More from this journal
- Volume:
- 58
- Issue:
- 5
- Pages:
- 609-618
- Publication date:
- 2014-03-01
- DOI:
- EISSN:
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1537-6591
- ISSN:
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1058-4838
- Language:
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English
- Keywords:
- Pubs id:
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pubs:452004
- UUID:
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uuid:b8af9df1-2acc-4f62-941a-8868124e6eca
- Local pid:
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pubs:452004
- Source identifiers:
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452004
- Deposit date:
-
2014-05-12
Terms of use
- Copyright holder:
- Price et al
- Copyright date:
- 2014
- Notes:
-
Copyright © The Author 2013. Published by Oxford University Press on behalf of the Infectious Diseases Society of America.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
- Licence:
- CC Attribution (CC BY)
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