Please use this identifier to cite or link to this item: https://doi.org/10.1056/NEJMoa1109910
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dc.titleRapid whole-genome sequencing for investigation of a neonatal MRSA outbreak
dc.contributor.authorKöser, C.U.
dc.contributor.authorHolden, M.T.G.
dc.contributor.authorEllington, M.J.
dc.contributor.authorCartwright, E.J.P.
dc.contributor.authorBrown, N.M.
dc.contributor.authorOgilvy-Stuart, A.L.
dc.contributor.authorHsu, L.Y.
dc.contributor.authorChewapreecha, C.
dc.contributor.authorCroucher, N.J.
dc.contributor.authorHarris, S.R.
dc.contributor.authorSanders, M.
dc.contributor.authorEnright, M.C.
dc.contributor.authorDougan, G.
dc.contributor.authorBentley, S.D.
dc.contributor.authorParkhill, J.
dc.contributor.authorFraser, L.J.
dc.contributor.authorBetley, J.R.
dc.contributor.authorSchulz-Trieglaff, O.B.
dc.contributor.authorSmith, G.P.
dc.contributor.authorPeacock, S.J.
dc.date.accessioned2016-09-06T08:42:03Z
dc.date.available2016-09-06T08:42:03Z
dc.date.issued2012-06-14
dc.identifier.issn00284793
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/126843
dc.description.abstractBACKGROUND: Isolates of methicillin-resistant Staphylococcus aureus (MRSA) belonging to a single lineage are often indistinguishable by means of current typing techniques. Whole-genome sequencing may provide improved resolution to define transmission pathways and characterize outbreaks. METHODS: We investigated a putative MRSA outbreak in a neonatal intensive care unit. By using rapid high-throughput sequencing technology with a clinically relevant turnaround time, we retrospectively sequenced the DNA from seven isolates associated with the outbreak and another seven MRSA isolates associated with carriage of MRSA or bacteremia in the same hospital. RESULTS:We constructed a phylogenetic tree by comparing single-nucleotide polymorphisms (SNPs) in the core genome to a reference genome (an epidemic MRSA clone, EMRSA-15 [sequence type 22]). This revealed a distinct cluster of outbreak isolates and clear separation between these and the nonoutbreak isolates. A previously missed transmission event was detected between two patients with bacteremia who were not part of the outbreak. We created an artificial "resistome" of antibiotic-resistance genes and demonstrated concordance between it and the results of phenotypic susceptibility testing; we also created a "toxome" consisting of toxin genes. One outbreak isolate had a hypermutator phenotype with a higher number of SNPs than the other outbreak isolates, highlighting the difficulty of imposing a simple threshold for the number of SNPs between isolates to decide whether they are part of a recent transmission chain. CONCLUSIONS: Whole-genome sequencing can provide clinically relevant data within a time frame that can influence patient care. The need for automated data interpretation and the provision of clinically meaningful reports represent hurdles to clinical implementation. (Funded by the U.K. Clinical Research Collaboration Translational Infection Research Initiative and others.). Copyright © 2012 Massachusetts Medical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1056/NEJMoa1109910
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.1056/NEJMoa1109910
dc.description.sourcetitleNew England Journal of Medicine
dc.description.volume366
dc.description.issue24
dc.description.page2267-2275
dc.description.codenNEJMA
dc.identifier.isiutNOT_IN_WOS
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