<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Jarocki VM</submitter><funding>Australian Research Council</funding><pubmed_abstract>Enterotoxigenic &lt;i>Escherichia coli&lt;/i> (ETEC) is the primary aetiologic agent of traveller's diarrhoea and a significant cause of diarrhoeal disease and death in developing countries. ETEC O169:H41 strains are known to cause both traveller's diarrhoea and foodborne outbreaks in developed countries and are cause for concern. Here, whole-genome sequencing (WGS) was used to assemble 46 O169:H41 (ST182) &lt;i>E. coli&lt;/i> draft genomes derived from two airplane waste samples sourced from a German international airport. The ST182 genomes were compared with all 84 publicly available, geographically diverse ST182 genomes to construct a core genome-based phylogenetic tree. ST182 isolates were all phylogroup E, the majority serotype O169:H41 (&lt;i>n&lt;/i> = 121, 93%) and formed five major clades. The airplane waste isolates differed by an average of 15 core SNPs (range 0-45) but their accessory genome content was diverse. While uncommon in other ST182 genomes, all airplane-derived ST182 isolates carried: (i) extended-spectrum β-lactamase gene &lt;i>bla&lt;/i> &lt;sub>CTX-M-&lt;/sub> &lt;sub>15&lt;/sub> notably lacking the typical adjacent IS&lt;i>Ecp1&lt;/i>; (ii) &lt;i>qnrS1&lt;/i> and the S83L mutation in &lt;i>gyrA&lt;/i>, both conferring resistance to fluoroquinolones; and (iii) a class 1 integron structure (IS&lt;i>26&lt;/i>-&lt;i>intI1&lt;/i> &lt;sub>Δ&lt;/sub> &lt;sub>648&lt;/sub>-&lt;i>dfrA17&lt;/i>-&lt;i>aadA5&lt;/i>-&lt;i>qacE&lt;/i>Δ&lt;i>1&lt;/i>-&lt;i>sul1&lt;/i>-ORF-&lt;i>srpC&lt;/i>-&lt;i>padR&lt;/i>-IS&lt;i>6100&lt;/i>-&lt;i>mphR&lt;/i>-&lt;i>mrx&lt;/i>-&lt;i>mphA&lt;/i>-IS&lt;i>26&lt;/i>) identified previously in major extraintestinal pathogenic &lt;i>E. coli&lt;/i> STs but not in ETEC. ST182 isolates carried ETEC-specific virulence factors STp + CS6. Adhesin/invasin &lt;i>tia&lt;/i> was identified in 89% of aircraft ST182 isolates (vs 23%) and was located on a putative genomic island within a hotspot region for various insertions including PAI I&lt;sub>536&lt;/sub> and plasmid-associated transposons. The most common plasmid replicons in this collection were IncFII (100%; F2:A-:B-) and IncB/O/K/Z (89%). Our data suggest that potentially through travel, &lt;i>E. coli&lt;/i> ST182 are evolving a multidrug-resistant profile through the acquisition of class 1 integrons and different plasmids.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>731050</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8454413</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multidrug-Resistant Lineage of Enterotoxigenic &lt;i>Escherichia coli&lt;/i> ST182 With Serotype O169:H41 in Airline Waste.</pubmed_title><pmcid>PMC8454413</pmcid><pubmed_authors>Heß S</pubmed_authors><pubmed_authors>Berendonk TU</pubmed_authors><pubmed_authors>Anantanawat K</pubmed_authors><pubmed_authors>Djordjevic SP</pubmed_authors><pubmed_authors>Jarocki VM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multidrug-Resistant Lineage of Enterotoxigenic &lt;i>Escherichia coli&lt;/i> ST182 With Serotype O169:H41 in Airline Waste.</name><description>Enterotoxigenic &lt;i>Escherichia coli&lt;/i> (ETEC) is the primary aetiologic agent of traveller's diarrhoea and a significant cause of diarrhoeal disease and death in developing countries. ETEC O169:H41 strains are known to cause both traveller's diarrhoea and foodborne outbreaks in developed countries and are cause for concern. Here, whole-genome sequencing (WGS) was used to assemble 46 O169:H41 (ST182) &lt;i>E. coli&lt;/i> draft genomes derived from two airplane waste samples sourced from a German international airport. The ST182 genomes were compared with all 84 publicly available, geographically diverse ST182 genomes to construct a core genome-based phylogenetic tree. ST182 isolates were all phylogroup E, the majority serotype O169:H41 (&lt;i>n&lt;/i> = 121, 93%) and formed five major clades. The airplane waste isolates differed by an average of 15 core SNPs (range 0-45) but their accessory genome content was diverse. While uncommon in other ST182 genomes, all airplane-derived ST182 isolates carried: (i) extended-spectrum β-lactamase gene &lt;i>bla&lt;/i> &lt;sub>CTX-M-&lt;/sub> &lt;sub>15&lt;/sub> notably lacking the typical adjacent IS&lt;i>Ecp1&lt;/i>; (ii) &lt;i>qnrS1&lt;/i> and the S83L mutation in &lt;i>gyrA&lt;/i>, both conferring resistance to fluoroquinolones; and (iii) a class 1 integron structure (IS&lt;i>26&lt;/i>-&lt;i>intI1&lt;/i> &lt;sub>Δ&lt;/sub> &lt;sub>648&lt;/sub>-&lt;i>dfrA17&lt;/i>-&lt;i>aadA5&lt;/i>-&lt;i>qacE&lt;/i>Δ&lt;i>1&lt;/i>-&lt;i>sul1&lt;/i>-ORF-&lt;i>srpC&lt;/i>-&lt;i>padR&lt;/i>-IS&lt;i>6100&lt;/i>-&lt;i>mphR&lt;/i>-&lt;i>mrx&lt;/i>-&lt;i>mphA&lt;/i>-IS&lt;i>26&lt;/i>) identified previously in major extraintestinal pathogenic &lt;i>E. coli&lt;/i> STs but not in ETEC. ST182 isolates carried ETEC-specific virulence factors STp + CS6. Adhesin/invasin &lt;i>tia&lt;/i> was identified in 89% of aircraft ST182 isolates (vs 23%) and was located on a putative genomic island within a hotspot region for various insertions including PAI I&lt;sub>536&lt;/sub> and plasmid-associated transposons. The most common plasmid replicons in this collection were IncFII (100%; F2:A-:B-) and IncB/O/K/Z (89%). Our data suggest that potentially through travel, &lt;i>E. coli&lt;/i> ST182 are evolving a multidrug-resistant profile through the acquisition of class 1 integrons and different plasmids.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2024-11-06T05:19:00.432Z</modification><creation>2022-02-11T11:19:13.01Z</creation></dates><accession>S-EPMC8454413</accession><cross_references><pubmed>34557175</pubmed><doi>10.3389/fmicb.2021.731050</doi></cross_references></HashMap>