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Genomic study of European Clostridioides difficile ribotype 002/ sequence type 8

dc.contributor.authorDost, Ines
dc.contributor.authorAbdel-Glil, Mostafa
dc.contributor.authorPersson, Soren
dc.contributor.authorConza, Karen
dc.contributor.authorOleastro, Mónica
dc.contributor.authorAlves, Frederico
dc.contributor.authorMaurischat, Sven
dc.contributor.authorScholtzek, Anissa
dc.contributor.authorSeyboldt, Christian
dc.date.accessioned2025-04-02T14:03:40Z
dc.date.available2025-04-02T14:03:40Z
dc.date.issued2024-07-25
dc.description.abstractClostridioides difficile has significant clinical importance as a leading cause of healthcare-associated infections, with symptoms ranging from mild diarrhoea to severe colitis, and possible life-threatening complications. C. difficile ribotype (RT) 002, mainly associated with MLST sequence type (ST) 8, is one of the most common RTs found in humans. This study aimed at investigating the genetic characteristics of 537 C. difficile genomes of ST8/RT002. To this end, we sequenced 298 C. difficile strains representing a new European genome collection, with strains from Germany, Denmark, France and Portugal. These sequences were analysed against a global dataset consisting of 1,437 ST8 genomes available through Enterobase. Our results showed close genetic relatedness among the studied ST8 genomes, a diverse array of antimicrobial resistance (AMR) genes and the presence of multiple mobile elements. Notably, the pangenome analysis revealed an open genomic structure. ST8 shows relatively low overall variation. Thus, clonal isolates were found across different One Health sectors (humans, animals, environment and food), time periods, and geographical locations, suggesting the lineage's stability and a universal environmental source. Importantly, this stability did not hinder the acquisition of AMR genes, emphasizing the adaptability of this bacterium to different selective pressures. Although only 2.4 % (41/1,735) of the studied genomes originated from non-human sources, such as animals, food, or the environment, we identified 9 cross-sectoral core genome multilocus sequence typing (cgMLST) clusters. Our study highlights the importance of ST8 as a prominent lineage of C. difficile with critical implications in the context of One Health. In addition, these findings strongly support the need for continued surveillance and investigation of non-human samples to gain a more comprehensive understanding of the epidemiology of C. difficile.eng
dc.description.sponsorshipThis work was supported by funding from the European Union’s Horizon 2020 Research and Innovation programme under grant agreement no. 773830: One Health European Joint Programme.
dc.identifier.citationMicrob Genom. 2024 Jul;10(7):001270. doi: 10.1099/mgen.0.001270
dc.identifier.doi10.1099/mgen.0.001270
dc.identifier.eissn2057-5858
dc.identifier.pmid39051872
dc.identifier.urihttp://hdl.handle.net/10400.18/10468
dc.language.isoeng
dc.peerreviewedyes
dc.publisherMicrobiology Society
dc.relationPromoting One Health in Europe through joint actions on foodborne zoonoses, antimicrobial resistance and emerging microbiological hazards.
dc.relation.hasversionhttps://www.microbiologyresearch.org/content/journal/mgen/10.1099/mgen.0.001270
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectClostridioides difficile
dc.subjectRibotype 002/ST8
dc.subjectGenomics
dc.subjectOne Health
dc.subjectGenomes
dc.subjectPhylogenetic Analysis
dc.subjectZoonotic Pathogen
dc.subjectAMR
dc.subjectInfecções Gastrointestinais
dc.titleGenomic study of European Clostridioides difficile ribotype 002/ sequence type 8por
dc.typeclinical study
dspace.entity.typePublication
oaire.awardTitlePromoting One Health in Europe through joint actions on foodborne zoonoses, antimicrobial resistance and emerging microbiological hazards.
oaire.awardURIinfo:eu-repo/grantAgreement/EC/H2020/773830/EU
oaire.citation.issue7
oaire.citation.startPage001270
oaire.citation.titleMicrobial Genomics
oaire.citation.volume10
oaire.fundingStreamH2020
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85
project.funder.identifierhttp://doi.org/10.13039/501100008530
project.funder.nameEuropean Commission
relation.isProjectOfPublication94d118fb-33ce-49fa-b1ed-d5bddf63581d
relation.isProjectOfPublication.latestForDiscovery94d118fb-33ce-49fa-b1ed-d5bddf63581d

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