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dc.contributor.authorButler, J
dc.contributor.authorKelly, SD
dc.contributor.authorMuddiman, KJ
dc.contributor.authorBesinis, A
dc.contributor.authorUpton, M
dc.date.accessioned2022-10-20T13:31:40Z
dc.date.issued2022-02-03
dc.date.updated2022-10-20T12:59:29Z
dc.description.abstractIntroduction. Cupriavidus pauculus is historically found in soil and water but has more recently been reported to cause human infection and death. Hospital sink traps can serve as a niche for bacterial persistence and a platform for horizontal gene transfer, with evidence of dissemination of pathogens in hospital plumbing systems driving nosocomial infection.Gap Statement. This paper presents the first C. pauculus strain isolated from a hospital sink trap. There are only six genome assemblies available on NCBI for C. pauculus; two of these are PacBio/Illumina hybrids. This paper presents the first ONT/Illumina hybrid assembly, with five contigs. The other assemblies available consist of 37, 38, 111 and 227 contigs. This paper also presents data on biofilm formation and lethal dose in Galleria mellonella; there is little published information describing these aspects of virulence.Aim. The aims were to identify the isolate found in a hospital sink trap, characterize its genome, and assess whether it could pose a risk to human health.Methodology. The genome was sequenced, and a hybrid assembly of short and long reads produced. Antimicrobial susceptibility was determined by the broth microdilution method. Virulence was assessed by measuring in vitro biofilm formation compared to Pseudomonas aeruginosa and in vivo lethality in Galleria mellonella larvae.Results. The isolate was confirmed to be a strain of C. pauculus, with a 6.8 Mb genome consisting of 6468 coding sequences and an overall G+C content of 63.9 mol%. The genome was found to contain 12 antibiotic resistance genes, 8 virulence factor genes and 33 metal resistance genes. The isolate can be categorized as resistant to meropenem, amoxicillin, amikacin, gentamicin and colistin, but susceptible to cefotaxime, cefepime, imipenem and ciprofloxacin. Clear biofilm formation was seen in all conditions over 72 h and exceeded that of P. aeruginosa when measured at 37 °C in R2A broth. Lethality in G. mellonella larvae over 48 h was relatively low.Conclusion. The appearance of a multidrug-resistant strain of C. pauculus in a known pathogen reservoir within a clinical setting should be considered concerning. Further work should be completed to compare biofilm formation and in vivo virulence between clinical and environmental strains, to determine how easily environmental strains may establish human infection. Infection control teams and clinicians should be aware of the emerging nature of this pathogen and further work is needed to minimize the impact of contaminated hospital plumbing systems on patient outcomes.en_GB
dc.format.extent001501-
dc.format.mediumPrint
dc.identifier.citationVol. 71(2), article 001501en_GB
dc.identifier.doihttps://doi.org/10.1099/jmm.0.001501
dc.identifier.urihttp://hdl.handle.net/10871/131349
dc.identifierORCID: 0000-0003-1998-1219 (Butler, James)
dc.language.isoenen_GB
dc.publisherMicrobiology Societyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/35113779en_GB
dc.rights© 2022 The Authors This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/en_GB
dc.subjectCupriavidus pauculusen_GB
dc.subjectGalleria mellonellaen_GB
dc.subjectMF1en_GB
dc.subjectSink trapen_GB
dc.subjectbiofilmen_GB
dc.subjectwhole genome sequencingen_GB
dc.titleHospital sink traps as a potential source of the emerging multidrug-resistant pathogen Cupriavidus pauculus: characterization and draft genome sequence of strain MF1en_GB
dc.typeArticleen_GB
dc.date.available2022-10-20T13:31:40Z
dc.identifier.issn0022-2615
exeter.article-numberARTN 001501
exeter.place-of-publicationEngland
dc.descriptionThis is the final version. Available on open access from the Microbiology Society via the DOI in this recorden_GB
dc.descriptionData availability: This project has been deposited at DDBJ/ENA/GenBank under the accession JAIQWY000000000 within BioProject PRJNA762702. The version described in this paper is version JAIQWY010000000. The contig sequences can be found under accession numbers JAIQWY010000001–JAIQWY010000005. Raw sequence data have been deposited under accession numbers SRX13365403 and SRX13365404. Four supplementary tables are available with the online version of this article.en_GB
dc.identifier.eissn1473-5644
dc.identifier.journalJournal of Medical Microbiologyen_GB
dc.relation.ispartofJ Med Microbiol, 71(2)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2021-12-29
dc.rights.licenseCC BY
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2022-02-03
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-10-20T13:28:20Z
refterms.versionFCDVoR
refterms.dateFOA2022-10-20T13:31:45Z
refterms.panelAen_GB


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© 2022 The Authors This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/
Except where otherwise noted, this item's licence is described as © 2022 The Authors This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/