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dc.contributor.authorBurke, D.G.
dc.contributor.authorHarrison, M.J.
dc.contributor.authorFleming, C.
dc.contributor.authorMcCarthy, M.
dc.contributor.authorShortt, C.
dc.contributor.authorSulaiman, I.
dc.contributor.authorMurphy, D.M.
dc.contributor.authorEustace, J.A.
dc.contributor.authorShanahan, F.
dc.contributor.authorHill, C.
dc.contributor.authorStanton, C.
dc.contributor.authorRea, M.C.
dc.contributor.authorRoss, R.P.
dc.contributor.authorPlant, B.J.
dc.date.accessioned2023-10-10T15:00:33Z
dc.date.available2023-10-10T15:00:33Z
dc.date.issued2017-03
dc.identifier.citationD.G. Burke, M.J. Harrison, C. Fleming, M. McCarthy, C. Shortt, I. Sulaiman, D.M. Murphy, J.A. Eustace, F. Shanahan, C. Hill, C. Stanton, M.C. Rea, R.P. Ross, B.J. Plant, Clostridium difficile carriage in adult cystic fibrosis (CF); implications for patients with CF and the potential for transmission of nosocomial infection, Journal of Cystic Fibrosis, Volume 16, Issue 2, 2017, Pages 291-298, ISSN 1569-1993, https://doi.org/10.1016/j.jcf.2016.09.008.en_US
dc.identifier.urihttp://hdl.handle.net/11019/3335
dc.descriptionpeer-revieweden_US
dc.description.abstractClostridium difficile is an anaerobic Gram-positive, spore-forming, toxin-producing bacillus transmitted among humans through the faecal–oral route. Despite increasing carriage rates and the presence of C. difficile toxin in stool, patients with CF rarely appear to develop typical manifestations of C. difficile infection (CDI). In this study, we examined the carriage, toxin production, ribotype distribution and antibiotic susceptibility of C. difficile in a cohort of 60 adult patients with CF who were pre-lung transplant. C. difficile was detected in 50% (30/60) of patients with CF by culturing for the bacteria. C. difficile toxin was detected in 63% (19/30) of C. difficile-positive stool samples. All toxin-positive stool samples contained toxigenic C. difficile strains harbouring toxin genes, tcdA and tcdB. Despite the presence of C. difficile and its toxin in patient stool, no acute gastrointestinal symptoms were reported. Ribotyping of C. difficile strains revealed 16 distinct ribotypes (RT), 11 of which are known to be disease-causing including the hyper-virulent RT078. Additionally, strains RT002, RT014, and RT015, which are common in non-CF nosocomial infection were described. All strains were susceptible to vancomycin, metronidazole, fusidic acid and rifampicin. No correlation was observed between carriage of C. difficile or any characteristics of isolated strains and any recorded clinical parameters or treatment received. We demonstrate a high prevalence of hypervirulent, toxigenic strains of C. difficile in asymptomatic patients with CF. This highlights the potential role of asymptomatic patients with CF in nosocomial transmission of C. difficile.en_US
dc.description.sponsorshipScience Foundation Ireland
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesJournal of Cystic Fibrosis;Vol 16
dc.rights© 2016 European Cystic Fibrosis Society. Published by Elsevier B.V.
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttps://www.elsevier.com/tdm/userlicense/1.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectClostridium difficileen_US
dc.subjectCystic fibrosisen_US
dc.subjectTransmissionen_US
dc.subjectNosocomial infectionen_US
dc.titleClostridium difficile carriage in adult cystic fibrosis (CF); implications for patients with CF and the potential for transmission of nosocomial infectionen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1016/j.jcf.2016.09.008
dc.contributor.sponsorScience Foundation Irelanden_US
dc.contributor.sponsorEuropean Union Seventh Framework Programmeen_US
dc.contributor.sponsorScience Foundation Irelanden_US
dc.contributor.sponsorGrantNumber02/CE/B124en_US
dc.contributor.sponsorGrantNumber603038en_US
dc.contributor.sponsorGrantNumberSFI/12/RC/2273en_US
dc.source.volume16
dc.source.issue2
dc.source.beginpage291
dc.source.endpage298
refterms.dateFOA2023-10-10T15:00:35Z
dc.source.journaltitleJournal of Cystic Fibrosis


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