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               <dc:title>Virulence genes and subclone status as markers of experimental virulence in a murine sepsis model among Escherichia coli sequence type 131 clinical isolates from Spain</dc:title>
               <dc:creator>Merino, Irene</dc:creator>
               <dc:creator>Porter, Stephen B.</dc:creator>
               <dc:creator>Johnston, Brian D.</dc:creator>
               <dc:creator>Clabots, Connie</dc:creator>
               <dc:creator>Shaw Perujo, Evelyn</dc:creator>
               <dc:creator>Horcajada Gallego, Juan Pablo</dc:creator>
               <dc:creator>Cantón, Rafael</dc:creator>
               <dc:creator>Ruiz Garbajosa, Patricia</dc:creator>
               <dc:creator>Johnson, James R.</dc:creator>
               <dc:subject>Septicèmia</dc:subject>
               <dc:subject>Escheríchia coli</dc:subject>
               <dc:subject>Septicemia</dc:subject>
               <dc:subject>Escherichia coli</dc:subject>
               <dc:description>Objective: To assess experimental virulence among sequence type 131 (ST131) Escherichia coli bloodstream isolates in relation to virulence genotype and subclone. Methods: We analysed 48 Spanish ST131 bloodstream isolates (2010) by PCR for ST131 subclone status (H30Rx, H30 non-Rx, or non-H30), virulence genes (VGs), and O-type. Then we compared these traits with virulence in a murine sepsis model, as measured by illness severity score (ISS) and rapid lethality (mean ISS >= 4). Results: Of the 48 study isolates, 65% were H30Rx, 21% H30 non-Rx, and 15% non-H30; 44% produced ESBLs, 98% were O25b, and 83% qualified as extraintestinal pathogenic E. coli (ExPEC). Of 49 VGs, ibeA and iss were associated significantly with non-H30 isolates, and sat, iha and malX with H30 isolates. Median VG scores differed by subclone, i.e., 12 (H30Rx), 10 (H30 non-Rx), and 11 (non-H30) (p &lt; 0.01). Nearly 80% of isolates represented a described virotype. In mice, H30Rx and non-H30 isolates were more virulent than H30 non-Rx isolates (according to ISS [p = 0.03] and rapid lethality [p = 0.03]), as were ExPEC isolates compared with non-ExPEC isolates (median ISS, 4.3 vs. 2.7: p = 0.03). In contrast, most individual VGs, VG scores, VG profiles, and virotypes were not associated with mouse virulence. Conclusions: ST131 subclone and ExPEC status, but not individual VGs, VG scores or profiles, or virotypes, predicted mouse virulence. Given the lower virulence of non-Rx H30 isolates, hyper-virulence probably cannot explain the ST131-H30 clade's epidemic emergence.</dc:description>
               <dc:date>2018-07-27T12:25:30Z</dc:date>
               <dc:date>2018-07-27T12:25:30Z</dc:date>
               <dc:date>2017-11-30</dc:date>
               <dc:date>2018-07-24T11:55:22Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0188838</dc:relation>
               <dc:relation>PLoS One, 2017, vol. 12, num. 11,p. e0188838</dc:relation>
               <dc:relation>http://dx.doi.org/10.1371/journal.pone.0188838</dc:relation>
               <dc:rights>cc by (c) Merino et al., 2017</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Public Library of Science (PLoS)</dc:publisher>
               <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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