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1000 Titel
  • The genetic relationship between human and pet isolates: a core genome multilocus sequence analysis of multidrug-resistant bacteria
1000 Autor/in
  1. Genath, Antonia |
  2. Hackmann, Carolin |
  3. Denkel, Luisa |
  4. Weber, Anna |
  5. Maechler, Friederike |
  6. Kola, Axel |
  7. Schwarz, Stefan |
  8. Gastmeier, Petra |
  9. Leistner, Rasmus |
1000 Verlag BioMed Central
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-09-20
1000 Erschienen in
1000 Quellenangabe
  • 13(1):107
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13756-024-01457-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11416027/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Introduction</jats:title> <jats:p>The global increase of multidrug-resistant organisms (MDROs) is one of the most urgent public health threats affecting both humans and animals. The One Health concept emphasizes the interconnectedness of human, animal and environmental health and highlights the need for integrated approaches to combat antimicrobial resistance (AMR). Although the sharing of environments and antimicrobial agents between companion animals and humans poses a risk for MDRO transmission, companion animals have been studied to a lesser extent than livestock animals. This study therefore used core genome multilocus sequence typing (cgMLST) to investigate the genetic relationships and putative transmission of MDROs between humans and pets.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>This descriptive integrated typing study included 252 human isolates, 53 dog isolates and 10 cat isolates collected from 2019 to 2022 at the Charité University Hospital in Berlin, Germany. CgMLST was performed to characterize methicillin-resistant <jats:italic>Staphylococcus aureus</jats:italic>, vancomycin-resistant enterococci and multidrug-resistant gram-negative bacteria. The genetic diversity of the MDROs of the different host populations was determined and compared based on sequence type and core genome complex type.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>Within this study the majority of samples from pets and humans was genetically distinct. However, for some isolates, the number of allelic differences identified by cgMLST was low. Two cases of putative household transmission or shared source of VR <jats:italic>E. faecium</jats:italic> and MDR <jats:italic>E. coli</jats:italic> between humans and pets were documented.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>The interaction between humans and their pets appears to play a minor role in the spread of the MDROs studied. However, further research is needed. This study emphasizes the importance of comprehensive molecular surveillance and a multidisciplinary One Health approach to understand and contain the spread of MDROs in human and animal populations.</jats:p> </jats:sec><jats:sec> <jats:title>Trial Registration</jats:title> <jats:p>The study is registered with the German Clinical Trials Register (DRKS00030009).</jats:p> </jats:sec>
1000 Sacherschließung
lokal Pets/microbiology [MeSH]
lokal Molecular typing
lokal Cats [MeSH]
lokal Humans [MeSH]
lokal One Health [MeSH]
lokal Genome, Bacterial [MeSH]
lokal Multidrug-resistance
lokal Vancomycin-Resistant Enterococci/genetics [MeSH]
lokal Animals [MeSH]
lokal Methicillin-Resistant Staphylococcus aureus/classification [MeSH]
lokal Dogs [MeSH]
lokal Methicillin-Resistant Staphylococcus aureus/genetics [MeSH]
lokal Research
lokal Anti-Bacterial Agents/pharmacology [MeSH]
lokal Germany [MeSH]
lokal Methicillin-Resistant Staphylococcus aureus/drug effects [MeSH]
lokal Multilocus Sequence Typing [MeSH]
lokal One Health
lokal Genetic Variation [MeSH]
lokal Microbial Sensitivity Tests [MeSH]
lokal cgMLST
lokal Drug Resistance, Multiple, Bacterial/genetics [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/R2VuYXRoLCBBbnRvbmlh|https://frl.publisso.de/adhoc/uri/SGFja21hbm4sIENhcm9saW4=|https://frl.publisso.de/adhoc/uri/RGVua2VsLCBMdWlzYQ==|https://frl.publisso.de/adhoc/uri/V2ViZXIsIEFubmE=|https://frl.publisso.de/adhoc/uri/TWFlY2hsZXIsIEZyaWVkZXJpa2U=|https://frl.publisso.de/adhoc/uri/S29sYSwgQXhlbA==|https://frl.publisso.de/adhoc/uri/U2Nod2FyeiwgU3RlZmFu|https://frl.publisso.de/adhoc/uri/R2FzdG1laWVyLCBQZXRyYQ==|https://frl.publisso.de/adhoc/uri/TGVpc3RuZXIsIFJhc211cw==
1000 Hinweis
  • DeepGreen-ID: 5ac6f827715148fab7f43fdf5b0d9df6 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Charité – Universitätsmedizin Berlin |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Charité – Universitätsmedizin Berlin |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6520379.rdf
1000 Erstellt am 2025-07-06T00:33:15.455+0200
1000 Erstellt von 322
1000 beschreibt frl:6520379
1000 Zuletzt bearbeitet 2025-08-07T08:57:29.839+0200
1000 Objekt bearb. Thu Aug 07 08:57:29 CEST 2025
1000 Vgl. frl:6520379
1000 Oai Id
  1. oai:frl.publisso.de:frl:6520379 |
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