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dc.contributor.authorPalmer, Kelli L.
dc.contributor.authorGodfrey, Paul
dc.contributor.authorGriggs, Allison
dc.contributor.authorKos, Veronica N.
dc.contributor.authorZucker, Jeremy
dc.contributor.authorDesjardins, Christopher A.
dc.contributor.authorCerqueira, Gustavo
dc.contributor.authorGevers, Dirk
dc.contributor.authorWalker, Suzanne
dc.contributor.authorWortman, Jennifer
dc.contributor.authorFeldgarden, Michael
dc.contributor.authorHaas, Brian J.
dc.contributor.authorBirren, Bruce W.
dc.contributor.authorGilmore, Michael S.
dc.date.accessioned2012-10-04T18:07:55Z
dc.date.available2012-10-04T18:07:55Z
dc.date.issued2012-02
dc.date.submitted2012-01
dc.identifier.issn2150-7511
dc.identifier.issn2150-7511
dc.identifier.urihttp://hdl.handle.net/1721.1/73611
dc.description.abstractThe enterococci are Gram-positive lactic acid bacteria that inhabit the gastrointestinal tracts of diverse hosts. However, Enterococcus faecium and E. faecalis have emerged as leading causes of multidrug-resistant hospital-acquired infections. The mechanism by which a well-adapted commensal evolved into a hospital pathogen is poorly understood. In this study, we examined high-quality draft genome data for evidence of key events in the evolution of the leading causes of enterococcal infections, including E. faecalis, E. faecium, E. casseliflavus, and E. gallinarum. We characterized two clades within what is currently classified as E. faecium and identified traits characteristic of each, including variation in operons for cell wall carbohydrate and putative capsule biosynthesis. We examined the extent of recombination between the two E. faecium clades and identified two strains with mosaic genomes. We determined the underlying genetics for the defining characteristics of the motile enterococci E. casseliflavus and E. gallinarum. Further, we identified species-specific traits that could be used to advance the detection of medically relevant enterococci and their identification to the species level. IMPORTANCE: The enterococci, in particular, vancomycin-resistant enterococci, have emerged as leading causes of multidrug-resistant hospital-acquired infections. In this study, we examined genome sequence data to define traits with the potential to influence host-microbe interactions and to identify sequences and biochemical functions that could form the basis for the rapid identification of enterococcal species or lineages of importance in clinical and environmental samples.en_US
dc.description.sponsorshipUnited States. Dept. of Health and Human Services (Grant AI072360)en_US
dc.description.sponsorshipUnited States. Dept. of Health and Human Services. Harvard-Wide Antibiotic Resistance Program (Grant AI083214)en_US
dc.description.sponsorshipUnited States. Dept. of Health and Human Services (Contract HHSN272200900018C)en_US
dc.language.isoen_US
dc.publisherAmerican Society for Microbiologyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1128/mBio.00318-11en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceAmerican Society for Microbiologyen_US
dc.titleComparative Genomics of Enterococci: Variation in Enterococcus faecalis, Clade Structure in E. faecium, and Defining Characteristics of E. gallinarum and E. casseliflavusen_US
dc.typeArticleen_US
dc.identifier.citationPalmer, K. L. et al. “Comparative Genomics of Enterococci: Variation in Enterococcus Faecalis, Clade Structure in E. Faecium, and Defining Characteristics of E. Gallinarum and E. Casseliflavus.” mBio 3.1 (2012): e00318–11–e00318–11. © 2012 Palmer et al.en_US
dc.contributor.mitauthorZucker, Jeremy
dc.contributor.mitauthorBirren, Bruce W.
dc.relation.journalmBioen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsPalmer, K. L.; Godfrey, P.; Griggs, A.; Kos, V. N.; Zucker, J.; Desjardins, C.; Cerqueira, G.; Gevers, D.; Walker, S.; Wortman, J.; Feldgarden, M.; Haas, B.; Birren, B.; Gilmore, M. S.en
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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