<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Butters A</submitter><funding>Beef Cattle Research Council (BCRC)</funding><funding>Beef Cattle Research Council</funding><funding>Canadian Government | Natural Sciences and Engineering Research Council of Canada (NSERC)</funding><funding>Results Driven Agricultural Research</funding><funding>Alberta Beef Producers</funding><funding>Alberta Beef Producers (ABP)</funding><funding>Canadian Government | Natural Sciences and Engineering Research Council of Canada</funding><pagination>e0053224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11451601</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(10)</volume><pubmed_abstract>Colistin resistance in &lt;i>Escherichia coli&lt;/i> is of public health significance for its use to treat multidrug-resistant Gram-negative infections. Amino acid variations in PmrB have been implicated in colistin resistance in &lt;i>E. coli&lt;/i>. In this cross-sectional study, 288 generic &lt;i>E. coli&lt;/i> isolates from surveillance of broiler chicken and feedlot cattle feces, retail meat, wastewater, and well water were whole-genome sequenced. Phylogroup designation and screening for two amino acid substitutions in PmrB putatively linked to colistin resistance (Y358N, E123D) were performed &lt;i>in silico&lt;/i>. Three additional data sets of publicly available &lt;i>E. coli&lt;/i> assemblies were similarly scrutinized: (i) &lt;i>E. coli&lt;/i> isolates from studies identifying the Y358N or E123D substitutions, (ii)</pubmed_abstract><journal>Microbiology spectrum</journal><pubmed_title>PmrB Y358N, E123D amino acid substitutions are not associated with colistin resistance but with phylogeny in &lt;i>Escherichia coli&lt;/i>.</pubmed_title><pmcid>PMC11451601</pmcid><funding_grant_id>RGPIN/05307-2019</funding_grant_id><funding_grant_id>ANH.29.20</funding_grant_id><funding_grant_id>2021R098R</funding_grant_id><funding_grant_id>2021R098RC</funding_grant_id><pubmed_authors>Checkley SL</pubmed_authors><pubmed_authors>Liljebjelke K</pubmed_authors><pubmed_authors>Butters A</pubmed_authors><pubmed_authors>Jovel J</pubmed_authors><pubmed_authors>Waldner C</pubmed_authors><pubmed_authors>Gow S</pubmed_authors></additional><is_claimable>false</is_claimable><name>PmrB Y358N, E123D amino acid substitutions are not associated with colistin resistance but with phylogeny in &lt;i>Escherichia coli&lt;/i>.</name><description>Colistin resistance in &lt;i>Escherichia coli&lt;/i> is of public health significance for its use to treat multidrug-resistant Gram-negative infections. Amino acid variations in PmrB have been implicated in colistin resistance in &lt;i>E. coli&lt;/i>. In this cross-sectional study, 288 generic &lt;i>E. coli&lt;/i> isolates from surveillance of broiler chicken and feedlot cattle feces, retail meat, wastewater, and well water were whole-genome sequenced. Phylogroup designation and screening for two amino acid substitutions in PmrB putatively linked to colistin resistance (Y358N, E123D) were performed &lt;i>in silico&lt;/i>. Three additional data sets of publicly available &lt;i>E. coli&lt;/i> assemblies were similarly scrutinized: (i) &lt;i>E. coli&lt;/i> isolates from studies identifying the Y358N or E123D substitutions, (ii)</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-06-08T03:31:24.137Z</modification><creation>2025-04-04T00:34:04.761Z</creation></dates><accession>S-EPMC11451601</accession><cross_references><pubmed>39162501</pubmed><doi>10.1128/spectrum.00532-24</doi></cross_references></HashMap>