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Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: An epidemiological model

dc.contributor.authorYakob, Laith
dc.contributor.authorRiley, Thomas
dc.contributor.authorPaterson, D L
dc.contributor.authorMarquess, John
dc.contributor.authorMagalhaes, Ricardo Soares
dc.contributor.authorFuruya Kanamori, Luis
dc.contributor.authorClements, Archie
dc.date.accessioned2015-12-13T22:36:30Z
dc.date.issued2015
dc.date.updated2015-12-11T09:32:08Z
dc.description.abstractFollowing rapid, global clonal dominance of hypervirulent ribotypes, Clostridium difficile now constitutes the primary infectious cause of nosocomial diarrhoea. Evidence indicates at least three possible mechanisms of hypervirulence that facilitates the successful invasion of these atypical strains: 1) increased infectiousness relative to endemic strains; 2) increased symptomatic disease rate relative to endemic strains; and 3) an ability to outcompete endemic strains in the host's gut. Stochastic simulations of an infection transmission model demonstrate clear differences between the invasion potentials of C. difficile strains utilising the alternative hypervirulence mechanisms, and provide new evidence that favours certain mechanisms (1 and 2) more than others (3). Additionally, simulations illustrate that direct competition between strains (inside the host's gut) is not a prerequisite for the sudden switching that has been observed in prevailing ribotypes; previously dominant C. difficile strains can be excluded by hypervirulent ribotypes through indirect (exploitative) competition.
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/1885/76791
dc.publisherNature Publishing Group
dc.rightsAuthor/s retain copyrighten_AU
dc.sourceScientific Reports
dc.titleMechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: An epidemiological model
dc.typeJournal article
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue12666
local.bibliographicCitation.lastpage9
local.bibliographicCitation.startpage1
local.contributor.affiliationYakob, Laith, London School of Hygiene & Tropical Medicine
local.contributor.affiliationRiley, Thomas, University of Western Australia
local.contributor.affiliationPaterson, D L, University of Queensland
local.contributor.affiliationMarquess, John, Centre for Healthcare Related Infection Surveillance and Prevention
local.contributor.affiliationMagalhaes, Ricardo Soares, The University of Queensland
local.contributor.affiliationClements, Archie, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationFuruya Kanamori, Luis, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidClements, Archie, u5611518
local.contributor.authoruidFuruya Kanamori, Luis, u5127170
local.description.notesImported from ARIES
local.identifier.absfor111706 - Epidemiology
local.identifier.ariespublicationU3488905xPUB5584
local.identifier.citationvolume5
local.identifier.doi10.1038/srep12666
local.identifier.scopusID2-s2.0-84938117616
local.type.statusPublished Version

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