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dc.contributor.authorTurner, Claire E.
dc.contributor.authorDryden, Matthew
dc.contributor.authorHolden, Matthew Thomas Geoffrey
dc.contributor.authorDavies, Frances J.
dc.contributor.authorLawrenson, Richard A.
dc.contributor.authorFarzaneh, Leili
dc.contributor.authorBentley, Stephen D.
dc.contributor.authorEfstratiou, Androulla
dc.contributor.authorSriskandan, Shiranee
dc.date.accessioned2014-07-08T11:01:01Z
dc.date.available2014-07-08T11:01:01Z
dc.date.issued2013-07
dc.identifier74259738
dc.identifier50d63523-6031-47f8-b0d4-71c72d9a1b25
dc.identifier000320595800012
dc.identifier84879426675
dc.identifier.citationTurner , C E , Dryden , M , Holden , M T G , Davies , F J , Lawrenson , R A , Farzaneh , L , Bentley , S D , Efstratiou , A & Sriskandan , S 2013 , ' Molecular analysis of an outbreak of lethal postpartum sepsis caused by Streptococcus pyogenes ' , Journal of Clinical Microbiology , vol. 51 , no. 7 , pp. 2089-2095 . https://doi.org/10.1128/JCM.00679-13en
dc.identifier.issn0095-1137
dc.identifier.otherORCID: /0000-0002-4958-2166/work/60196429
dc.identifier.urihttps://hdl.handle.net/10023/4964
dc.descriptionThis work was supported by the United Kingdom Clinical Research Collaboration, which funds the National Centre for Infection Prevention and Management at Imperial College London. The work was also supported by The Wellcome Trust (C.E.T., R.A.L., S.D.B., and M.T.G.H.). S.S. is grateful for support from the United Kingdom NIHR Biomedical Research Centre funding scheme.en
dc.description.abstractSepsis is now the leading direct cause of maternal death in the United Kingdom, and Streptococcus pyogenes is the leading pathogen. We combined conventional and genomic analyses to define the duration and scale of a lethal outbreak. Two postpartum deaths caused by S. pyogenes occurred within 24 h; one was characterized by bacteremia and shock and the other by hemorrhagic pneumonia. The women gave birth within minutes of each other in the same maternity unit 2 days earlier. Seven additional infections in health care and household contacts were subsequently detected and treated. All cluster-associated S. pyogenes isolates were genotype emm1 and were initially indistinguishable from other United Kingdom emm1 isolates. Sequencing of the virulence gene sic revealed that all outbreak isolates had the same unique sic type. Genome sequencing confirmed that the cluster was caused by a unique S. pyogenes clone. Transmission between patients occurred on a single day and was associated with casual contact only. A single isolate from one patient demonstrated a sequence change in sic consistent with longer infection duration. Transmission to health care workers was traced to single clinical contacts with index cases. The last case was detected 18 days after the first case. Following enhanced surveillance, the outbreak isolate was not detected again. Mutations in bacterial regulatory genes played no detectable role in this outbreak, illustrating the intrinsic ability of emm1 S. pyogenes to spread while retaining virulence. This fast-moving outbreak highlights the potential of S. pyogenes to cause a range of diseases in the puerperium with rapid transmission, underlining the importance of immediate recognition and response by clinical infection and occupational health teams.
dc.format.extent7
dc.format.extent661356
dc.language.isoeng
dc.relation.ispartofJournal of Clinical Microbiologyen
dc.subjectGroup-a streptococcusen
dc.subjectComplement-inhibiting proteinen
dc.subjectHealth-careen
dc.subjectInfectionsen
dc.subjectSelectionen
dc.subjectCariageen
dc.subjectDiseaseen
dc.subjectGeneen
dc.subjectSurveillanceen
dc.subjectPreventionen
dc.subjectQR Microbiologyen
dc.subject.lccQRen
dc.titleMolecular analysis of an outbreak of lethal postpartum sepsis caused by Streptococcus pyogenesen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Infection Groupen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doi10.1128/JCM.00679-13
dc.description.statusPeer revieweden


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