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dc.contributor.authorWard, Philip N.
dc.contributor.authorHolden, Matthew T. G.
dc.contributor.authorLeigh, James A.
dc.contributor.authorLennard, Nicola
dc.contributor.authorBignell, Alexandra
dc.contributor.authorBarron, Andy
dc.contributor.authorClark, Louise
dc.contributor.authorQuail, Michael A.
dc.contributor.authorWoodward, John
dc.contributor.authorBarrell, Bart G.
dc.contributor.authorEgan, Sharon A.
dc.contributor.authorField, Terence R.
dc.contributor.authorMaskell, Duncan
dc.contributor.authorKehoe, Michael
dc.contributor.authorDowson, Christopher G.
dc.contributor.authorChanter, Neil
dc.contributor.authorWhatmore, Adrian M.
dc.contributor.authorBentley, Stephen D.
dc.contributor.authorParkhill, Julian
dc.date.accessioned2014-04-28T15:31:02Z
dc.date.available2014-04-28T15:31:02Z
dc.date.issued2009-01-28
dc.identifier91770899
dc.identifier20b5b35f-de9b-4655-a8d6-a4aad4873ea0
dc.identifier000264971000001
dc.identifier62749122218
dc.identifier.citationWard , P N , Holden , M T G , Leigh , J A , Lennard , N , Bignell , A , Barron , A , Clark , L , Quail , M A , Woodward , J , Barrell , B G , Egan , S A , Field , T R , Maskell , D , Kehoe , M , Dowson , C G , Chanter , N , Whatmore , A M , Bentley , S D & Parkhill , J 2009 , ' Evidence for niche adaptation in the genome of the bovine pathogen Streptococcus uberis ' , BMC Genomics , vol. 10 , 54 . https://doi.org/10.1186/1471-2164-10-54en
dc.identifier.issn1471-2164
dc.identifier.urihttps://hdl.handle.net/10023/4640
dc.descriptionThis work was supported by the Wellcome Trust.en
dc.description.abstractBackground: Streptococcus uberis, a Gram positive bacterial pathogen responsible for a significant proportion of bovine mastitis in commercial dairy herds, colonises multiple body sites of the cow including the gut, genital tract and mammary gland. Comparative analysis of the complete genome sequence of S. uberis strain 0140J was undertaken to help elucidate the biology of this effective bovine pathogen. Results: The genome revealed 1,825 predicted coding sequences (CDSs) of which 62 were identified as pseudogenes or gene fragments. Comparisons with related pyogenic streptococci identified a conserved core (40%) of orthologous CDSs. Intriguingly, S. uberis 0140J displayed a lower number of mobile genetic elements when compared with other pyogenic streptococci, however bacteriophage-derived islands and a putative genomic island were identified. Comparative genomics analysis revealed most similarity to the genomes of Streptococcus agalactiae and Streptococcus equi subsp. zooepidemicus. In contrast, streptococcal orthologs were not identified for 11% of the CDSs, indicating either unique retention of ancestral sequence, or acquisition of sequence from alternative sources. Functions including transport, catabolism, regulation and CDSs encoding cell envelope proteins were over-represented in this unique gene set; a limited array of putative virulence CDSs were identified. Conclusion: S. uberis utilises nutritional flexibility derived from a diversity of metabolic options to successfully occupy a discrete ecological niche. The features observed in S. uberis are strongly suggestive of an opportunistic pathogen adapted to challenging and changing environmental parameters.
dc.format.extent17
dc.format.extent2211314
dc.language.isoeng
dc.relation.ispartofBMC Genomicsen
dc.subjectGroup-a streptococcusen
dc.subjectGram-positive bacteriaen
dc.subjectGroup-b streptococcusen
dc.subjectComplete nucleotide-sequenceen
dc.subjectHyaluronic-acid capsuleen
dc.subjectClinical mastitisen
dc.subjectInorganic polyphosphateen
dc.subjectPlasminogen-activatoren
dc.subjectRepetitive structureen
dc.subjectMaximum-likelihooden
dc.subjectQH426 Geneticsen
dc.subjectQL Zoologyen
dc.subject.lccQH426en
dc.subject.lccQLen
dc.titleEvidence for niche adaptation in the genome of the bovine pathogen Streptococcus uberisen
dc.typeJournal itemen
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.doi10.1186/1471-2164-10-54
dc.description.statusPeer revieweden


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