Global phylogenomics of multidrug-resistant Salmonella enterica serotype Kentucky ST198

Research output: Contribution to journalJournal article – Annual report year: 2019Researchpeer-review

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  • Author: Hawkey, Jane

    Monash University, Australia

  • Author: Le Hello, Simon

    Institut Pasteur, France

  • Author: Doublet, Benoît

    Université de Tours, France

  • Author: Granier, Sophie A.

    Universite Paris-Est, France

  • Author: Hendriksen, Rene S.

    Research group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Kemitorvet, 2800, Kgs. Lyngby, Denmark

  • Author: Fricke, W Florian

    University of Hohenheim, Germany

  • Author: Ceyssens, Pieter-Jan

    Bacterial Diseases Unit, Belgium

  • Author: Gomart, Camille

    Institut Pasteur, France

  • Author: Billman-Jacobe, Helen

    University of Melbourne, Australia

  • Author: Holt, Kathryn E

    University of Melbourne, Australia

  • Author: Weill, Francois-Xavier

    Institut Pasteur, France

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Salmonella enterica serotype Kentucky can be a common causative agent of salmonellosis, usually associated with consumption of contaminated poultry. Antimicrobial resistance (AMR) to multiple drugs, including ciprofloxacin, is an emerging problem within this serotype. We used whole-genome sequencing (WGS) to investigate the phylogenetic structure and AMR content of 121 S.enterica serotype Kentucky sequence type 198 isolates from five continents. Population structure was inferred using phylogenomic analysis and whole genomes were compared to investigate changes in gene content, with a focus on acquired AMR genes. Our analysis showed that multidrug-resistant (MDR) S.enterica serotype Kentucky isolates belonged to a single lineage, which we estimate emerged circa 1989 following the acquisition of the AMR-associated Salmonella genomic island (SGI) 1 (variant SGI1-K) conferring resistance to ampicillin, streptomycin, gentamicin, sulfamethoxazole and tetracycline. Phylogeographical analysis indicates this clone emerged in Egypt before disseminating into Northern, Southern and Western Africa, then to the Middle East, Asia and the European Union. The MDR clone has since accumulated various substitution mutations in the quinolone-resistance-determining regions (QRDRs) of DNA gyrase (gyrA) and DNA topoisomerase IV (parC), such that most strains carry three QRDR mutations which together confer resistance to ciprofloxacin. The majority of AMR genes in the S. enterica serotype Kentucky genomes were carried either on plasmids or SGI structures. Remarkably, each genome of the MDR clone carried a different SGI1-K derivative structure; this variation could be attributed to IS26-mediated insertions and deletions, which appear to have hampered previous attempts to trace the clone's evolution using sub-WGS resolution approaches. Several different AMR plasmids were also identified, encoding resistance to chloramphenicol, third-generation cephalosporins, carbapenems and/or azithromycin. These results indicate that most MDR S. enterica serotype Kentucky circulating globally result from the clonal expansion of a single lineage that acquired chromosomal AMR genes 30 years ago, and has continued to diversify and accumulate additional resistances to last-line oral antimicrobials. This article contains data hosted by Microreact.
Original languageEnglish
JournalMicrobial Genomics
Volume5
Issue number7
Number of pages12
ISSN2057-5858
DOIs
Publication statusPublished - 2019
CitationsWeb of Science® Times Cited: No match on DOI

    Research areas

  • Salmonella, SGI, ST198, Phylogenomics, MDR, Kentucky

ID: 180023847