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dc.contributor.authorSteward, Karen Frances
dc.contributor.authorHarrison, Tihana
dc.contributor.authorRobinson, Carl
dc.contributor.authorSlater, Josh
dc.contributor.authorMaskell, Duncan J
dc.contributor.authorHarris, Simon R
dc.contributor.authorHolden, Matthew T G
dc.contributor.authorWaller, Andrew S
dc.date.accessioned2016-02-20T00:12:31Z
dc.date.available2016-02-20T00:12:31Z
dc.date.issued2015-05
dc.identifier.citationSteward , K F , Harrison , T , Robinson , C , Slater , J , Maskell , D J , Harris , S R , Holden , M T G & Waller , A S 2015 , ' PinR mediates the generation of reversible population diversity in Streptococcus zooepidemicus ' , Microbiology , vol. 161 , no. 5 , pp. 1105-1112 . https://doi.org/10.1099/mic.0.000057en
dc.identifier.issn1350-0872
dc.identifier.otherPURE: 174263266
dc.identifier.otherPURE UUID: 624fddd2-6b93-4148-ad69-e41ebc808465
dc.identifier.otherPubMed: 25701732
dc.identifier.otherScopus: 84991511073
dc.identifier.otherORCID: /0000-0002-4958-2166/work/60196401
dc.identifier.urihttps://hdl.handle.net/10023/8272
dc.descriptionThis project was funded by a project grant from the Horserace Betting Levy Board (vet/prj/751).en
dc.description.abstractOpportunistic pathogens must adapt to and survive in a wide range of complex ecosystems. Streptococcus zooepidemicus is an opportunistic pathogen of horses and many other animals, including man. The assembly of different surface architecture phenotypes from one genotype is likely to be crucial to the successful exploitation of such an opportunistic lifestyle. Construction of a series of mutants revealed that a serine recombinase, PinR, inverts 114 bp of the promoter of SZO_08560, which is bordered by GTAGACTTTA and TAAAGTCTAC inverted repeats. Inversion acts as a switch, controlling the transcription of this sortase-processed protein, which may enhance the attachment of S. zooepidemicus to equine trachea. The genome of a recently sequenced strain of S. zooepidemicus, strain 2329 (Sz2329), was found to contain a disruptive internal inversion of 7 kb of the FimIV pilus locus, which is bordered by TAGAAA and TTTCTA inverted repeats. This strain lacks pinR and we hypothesized that this inversion may have become irreversible following the loss of this recombinase. Active inversion of FimIV was detected in three strains of S. zooepidemicus: 1770 (Sz1770), B260863 (SzB260863) and H050840501 (SzH050840501), all of which encoded pinR. A deletion mutant of Sz1770 that lacked pinR was no longer capable of inverting its internal region of FimIV. Our data highlight redundancy in the PinR sequence recognition motif around a short TAGA consensus and suggest that PinR can reversibly influence the wider surface architecture of S. zooepidemicus, providing this organism with a bet-hedging solution to survival in fluctuating environments.
dc.language.isoeng
dc.relation.ispartofMicrobiologyen
dc.rightsCopyright 2015 The Authors. This is not the version of record of this article. This is an author accepted manuscript (AAM) that has been accepted for publication in Microbiology that has not been copy-edited, typeset or proofed. The Society for General Microbiology (SGM) does not permit the posting of AAMs for commercial use or systematic distribution. SGM disclaims any responsibility or liability for errors or omissions in this version of the manuscript or in any version derived from it by any other parties. The final version is available at 10.1099/mic.0.000057 2015.en
dc.subjectStreptococcus zooepedemicusen
dc.subjectPinRen
dc.subjectRecombinaseen
dc.subjectSurface proteinsen
dc.subjectR Medicineen
dc.subjectQR Microbiologyen
dc.subjectNDASen
dc.subject.lccRen
dc.subject.lccQRen
dc.titlePinR mediates the generation of reversible population diversity in Streptococcus zooepidemicusen
dc.typeJournal articleen
dc.description.versionPostprinten
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.doihttps://doi.org/10.1099/mic.0.000057
dc.description.statusPeer revieweden
dc.date.embargoedUntil2016-02-20


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