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dc.contributor.authorMoorhouse, AJ
dc.contributor.authorMoreno-Lopez, R
dc.contributor.authorGow, NAR
dc.contributor.authorHijazi, K
dc.date.accessioned2021-05-21T07:05:02Z
dc.date.issued2021-03-15
dc.description.abstractBackground:Candida species have long been recognised as aetiological agents of opportunistic infections of the oral mucosa, and more recently, as players of polymicrobial interactions driving caries, periodontitis and oral carcinogenesis. Methods: We studied the clonal structure of Candida spp. at oral niche resolution in patients (n = 20) with a range of oral health profiles over 22 months. Colonies from oral micro-environments were examined with multilocus sequencing typing. Results:Candida spp. identified were C. albicans, C. glabrata and C. dubliniensis. Increased propensity for micro-variations giving rise to multiple diploid strain types (DST), as a result of loss of heterozygosity, was observed among C. albicans clade 1 isolates compared to other clades. Micro-variations among isolates were also observed in C. dubliniensis contra to expectations of stable population structures for this species. Multiple sequence types were retrieved from patients without clinical evidence of oral candidosis, while single sequence types were isolated from oral candidosis patients. Conclusion: This is the first study to describe the clonal population structure, persistence and stability of Candida spp. at oral niche level. Future research investigating links between Candida spp. clonality and oral disease should recognise the propensity to micro-variations amongst oral niches in C. albicans and C. dubliniensis identified here.en_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.description.sponsorshipWellcome Trusten_GB
dc.identifier.citationVol. 13 (1), article 1894047en_GB
dc.identifier.doi10.1080/20002297.2021.1894047
dc.identifier.urihttp://hdl.handle.net/10871/125770
dc.language.isoenen_GB
dc.publisherTaylor & Francisen_GB
dc.rights© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectOral nicheen_GB
dc.subjectCandida albicansen_GB
dc.subjectC. glabrataen_GB
dc.subjectC. dubliniensisen_GB
dc.subjectMLSTen_GB
dc.subjectstrain typeen_GB
dc.subjectclonal evolutionen_GB
dc.titleClonal evolution of Candida albicans, Candida glabrata and Candida dubliniensis at oral niche level in health and diseaseen_GB
dc.typeArticleen_GB
dc.date.available2021-05-21T07:05:02Z
dc.descriptionThis is the final version. Available on open access from Taylor & Francis via the DOI in this recorden_GB
dc.identifier.eissn2000-2297
dc.identifier.journalJournal of Oral Microbiologyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2021-02-19
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2021-03-15
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2021-05-21T07:01:20Z
refterms.versionFCDVoR
refterms.dateFOA2021-05-21T07:05:53Z
refterms.panelAen_GB
refterms.depositExceptionpublishedGoldOA


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© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's licence is described as © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.