{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T18:56:37Z","timestamp":1792004197028,"version":"4.4.0"},"reference-count":74,"publisher":"Microbiology Society","issue":"7","license":[{"start":{"date-parts":[[2019,7,1]],"date-time":"2019-07-01T00:00:00Z","timestamp":1561939200000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2019,7,1]]},"abstract":"<jats:p>\n                    <jats:italic>\n                      <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.11017\" xlink:type=\"simple\">Salmonella enterica<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    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\n                    <jats:italic>S.<\/jats:italic>\n                    <jats:italic>e<\/jats:italic>\n                    <jats:italic>nterica<\/jats:italic>\n                    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)\n                    <jats:italic>S.<\/jats:italic>\n                    <jats:italic>enterica<\/jats:italic>\n                    serotype Kentucky isolates belonged to a single lineage, which we estimate emerged circa 1989 following the acquisition of the AMR-associated\n                    <jats:italic>\n                      <jats:named-content content-type=\"genus\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.3291\" xlink:type=\"simple\">Salmonella<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    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 (\n                    <jats:italic>gyrA<\/jats:italic>\n                    ) and DNA topoisomerase IV (\n                    <jats:italic>parC<\/jats:italic>\n                    ), such that most strains carry three QRDR mutations which together confer resistance to ciprofloxacin. The majority of AMR genes in the\n                    <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:actuate=\"onRequest\" content-type=\"species\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.11017\" xlink:role=\"http:\/\/doi.org\/10.1601\/about\" xlink:show=\"new\" xlink:title=\"Salmonella enterica\" xlink:type=\"simple\">\n                      <jats:italic>S<\/jats:italic>\n                      .\n                      <jats:italic>e<\/jats:italic>\n                      <jats:italic>nterica<\/jats:italic>\n                    <\/jats:named-content>\n                    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 IS\n                    <jats:italic>26<\/jats:italic>\n                    -mediated insertions and deletions, which appear to have hampered previous attempts to trace the clone\u2019s 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\n                    <jats:named-content xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:actuate=\"onRequest\" content-type=\"species\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.11017\" xlink:role=\"http:\/\/doi.org\/10.1601\/about\" xlink:show=\"new\" xlink:title=\"Salmonella enterica\" xlink:type=\"simple\">\n                      <jats:italic>S<\/jats:italic>\n                      .\n                      <jats:italic>e<\/jats:italic>\n                      <jats:italic>nterica<\/jats:italic>\n                    <\/jats:named-content>\n                    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\n                    <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/microreact.org\/showcase\" xlink:type=\"simple\">Microreact<\/jats:ext-link>\n                    .\n                  <\/jats:p>","DOI":"10.1099\/mgen.0.000269","type":"journal-article","created":{"date-parts":[[2019,5,20]],"date-time":"2019-05-20T11:13:11Z","timestamp":1558350791000},"source":"Crossref","is-referenced-by-count":91,"title":["Global phylogenomics of multidrug-resistant Salmonella enterica serotype Kentucky ST198"],"prefix":"10.1099","volume":"5","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9661-5293","authenticated-orcid":false,"given":"Jane","family":"Hawkey","sequence":"first","affiliation":[{"name":"Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville, Victoria 3010, Australia"},{"name":"Department of Infectious Diseases, Central Clinical School, Monash University, Melbourne, Victoria 3004, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Simon","family":"Le Hello","sequence":"additional","affiliation":[{"name":"Unit\u00e9 des Bact\u00e9ries Pathog\u00e8nes Ent\u00e9riques, Centre National de R\u00e9f\u00e9rence des \nEscherichia coli, \nShigella\n et \nSalmonella\n, World Health Organization Collaborative Centre for the Typing and Antibiotic Resistance of \nSalmonella\n, Institut Pasteur, 75015 Paris, France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0531-0967","authenticated-orcid":false,"given":"Beno\u00eet","family":"Doublet","sequence":"additional","affiliation":[{"name":"ISP, Institut National de la Recherche Agronomique, Universit\u00e9 Fran\u00e7ois Rabelais de Tours, UMR 1282, Nouzilly, France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9676-2402","authenticated-orcid":false,"given":"Sophie A.","family":"Granier","sequence":"additional","affiliation":[{"name":"Laboratoire de s\u00e9curit\u00e9 des aliments, Agence Nationale de S\u00e9curit\u00e9 Sanitaire de l'Alimentation, de l'Environnement et du Travail (ANSES), Universit\u00e9 PARIS-EST, 94701 Maisons-Alfort, France"},{"name":"Laboratoire de Foug\u00e8res, Agence Nationale de S\u00e9curit\u00e9 Sanitaire de l'Alimentation, de l'Environnement et du Travail (ANSES), 35306 Foug\u00e8res, France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2934-8214","authenticated-orcid":false,"given":"Rene S.","family":"Hendriksen","sequence":"additional","affiliation":[{"name":"Research Group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1586-0962","authenticated-orcid":false,"given":"W. Florian","family":"Fricke","sequence":"additional","affiliation":[{"name":"Department of Microbiome Research and Applied Bioinformatics, University of Hohenheim, Stuttgart, Germany"},{"name":"Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7735-8316","authenticated-orcid":false,"given":"Pieter-Jan","family":"Ceyssens","sequence":"additional","affiliation":[{"name":"Bacterial Diseases Unit, Sciensano, Brussels, Belgium"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4393-0422","authenticated-orcid":false,"given":"Camille","family":"Gomart","sequence":"additional","affiliation":[{"name":"Unit\u00e9 des Bact\u00e9ries Pathog\u00e8nes Ent\u00e9riques, Centre National de R\u00e9f\u00e9rence des \nEscherichia coli, \nShigella\n et \nSalmonella\n, World Health Organization Collaborative Centre for the 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