{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T00:07:19Z","timestamp":1791158839289,"version":"4.1.0"},"reference-count":38,"publisher":"American Society for Microbiology","issue":"6","license":[{"start":{"date-parts":[[2013,6,1]],"date-time":"2013-06-01T00:00:00Z","timestamp":1370044800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Clin Microbiol"],"published-print":{"date-parts":[[2013,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            We report the characteristics of 115 extended-spectrum beta-lactamase (ESBL)-producing\n            <jats:named-content content-type=\"genus-species\">Escherichia coli<\/jats:named-content>\n            clinical isolates, from 115 unique Danish patients, over a 1-year study interval (1 October 2008 to 30 September 2009). Forty-four (38%) of the ESBL isolates represented sequence type 131 (ST13)1, from phylogenetic group B2. The remaining 71 isolates were from phylogenetic groups D (27%), A (22%), B1 (10%), and B2 (3%). Serogroup O25 ST131 isolates (\n            <jats:italic>n<\/jats:italic>\n            = 42; 95% of ST131) comprised 7 different K antigens, whereas two ST131 isolates were O16:K100:H5. Compared to non-ST131 isolates, ST131 isolates were associated positively with CTX-M-15 and negatively with CTX-M-1 and CTX-M-14. They also were associated positively with 11 virulence genes, including\n            <jats:italic>afa<\/jats:italic>\n            and\n            <jats:italic>dra<\/jats:italic>\n            (Dr family adhesins), the F10\n            <jats:italic>papA<\/jats:italic>\n            allele (P fimbria variant),\n            <jats:italic>fimH<\/jats:italic>\n            (type 1 fimbriae),\n            <jats:italic>fyuA<\/jats:italic>\n            (yersiniabactin receptor),\n            <jats:italic>iha<\/jats:italic>\n            (adhesin siderophore),\n            <jats:italic>iutA<\/jats:italic>\n            (aerobactin receptor),\n            <jats:italic>kpsM<\/jats:italic>\n            II (group 2 capsules),\n            <jats:italic>malX<\/jats:italic>\n            (pathogenicity island marker),\n            <jats:italic>ompT<\/jats:italic>\n            (outer membrane protease),\n            <jats:italic>sat<\/jats:italic>\n            (secreted autotransporter toxin), and\n            <jats:italic>usp<\/jats:italic>\n            (uropathogenicity-specific protein) and negatively with\n            <jats:italic>hra<\/jats:italic>\n            (heat-resistant agglutinin) and\n            <jats:italic>iroN<\/jats:italic>\n            (salmochelin receptor). The consensus virulence gene profile (&gt;90% prevalence) of the ST131 isolates included\n            <jats:italic>fimH<\/jats:italic>\n            ,\n            <jats:italic>fyuA<\/jats:italic>\n            ,\n            <jats:italic>malX<\/jats:italic>\n            , and\n            <jats:italic>usp<\/jats:italic>\n            (100% each),\n            <jats:italic>ompT<\/jats:italic>\n            and the F10\n            <jats:italic>papA<\/jats:italic>\n            allele (95% each), and\n            <jats:italic>kpsM<\/jats:italic>\n            II and\n            <jats:italic>iutA<\/jats:italic>\n            (93% each). ST131 isolates were also positively associated with community acquisition, extraintestinal pathogenic\n            <jats:named-content content-type=\"genus-species\">E. coli<\/jats:named-content>\n            (ExPEC) status, and the O25, K100, and H4 antigens. Thus, among ESBL\n            <jats:named-content content-type=\"genus-species\">E. coli<\/jats:named-content>\n            isolates in Copenhagen, ST131 was the most prevalent clonal group, was community associated, and exhibited distinctive and comparatively extensive virulence profiles, plus a greater variety of capsular antigens than reported previously.\n          <\/jats:p>","DOI":"10.1128\/jcm.00346-13","type":"journal-article","created":{"date-parts":[[2013,4,4]],"date-time":"2013-04-04T06:34:49Z","timestamp":1365057289000},"page":"1779-1785","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":86,"title":["Prevalence and Characteristics of the Epidemic Multiresistant Escherichia coli ST131 Clonal Group among Extended-Spectrum Beta-Lactamase-Producing E. coli Isolates in Copenhagen, Denmark"],"prefix":"10.1128","volume":"51","author":[{"given":"Bente","family":"Olesen","sequence":"first","affiliation":[{"name":"Department of Clinical Microbiology, Hiller\u00f8d Hospital, Hiller\u00f8d, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dennis S.","family":"Hansen","sequence":"additional","affiliation":[{"name":"Department of Clinical Microbiology, Hiller\u00f8d Hospital, Hiller\u00f8d, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Frida","family":"Nilsson","sequence":"additional","affiliation":[{"name":"Department of Clinical Microbiology, Hiller\u00f8d Hospital, Hiller\u00f8d, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jakob","family":"Frimodt-M\u00f8ller","sequence":"additional","affiliation":[{"name":"Department of Clinical Microbiology, Hiller\u00f8d Hospital, Hiller\u00f8d, Denmark"},{"name":"Department of Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rikke Fleron","family":"Leihof","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carsten","family":"Struve","sequence":"additional","affiliation":[{"name":"WHO Collaborating Centre for Reference and Research on Escherichia and Klebsiella, Statens Serum Institut, Copenhagen, Denmark"},{"name":"Department of Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Flemming","family":"Scheutz","sequence":"additional","affiliation":[{"name":"WHO Collaborating Centre for Reference and Research on Escherichia and Klebsiella, Statens Serum Institut, Copenhagen, Denmark"},{"name":"Department of Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brian","family":"Johnston","sequence":"additional","affiliation":[{"name":"Veterans Affairs Medical Center and University of Minnesota, Minneapolis, Minnesota, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Karen A.","family":"Krogfelt","sequence":"additional","affiliation":[{"name":"WHO Collaborating Centre for Reference and Research on Escherichia and Klebsiella, Statens Serum Institut, Copenhagen, Denmark"},{"name":"Department of Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James R.","family":"Johnson","sequence":"additional","affiliation":[{"name":"Veterans Affairs Medical Center and University of Minnesota, Minneapolis, Minnesota, 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