<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Kieffer, Nicolas</dc:creator>
  <dc:creator>Royer, Guilhem</dc:creator>
  <dc:creator>Decousser, Jean-Winoc</dc:creator>
  <dc:creator>Bourrel, Anne-Sophie</dc:creator>
  <dc:creator>Palmieri, Mattia</dc:creator>
  <dc:creator>Ortiz de la Rosa, José Manuel</dc:creator>
  <dc:creator>Jacquier, Hervé</dc:creator>
  <dc:creator>Denamur, Erick</dc:creator>
  <dc:creator>Nordmann, Patrice</dc:creator>
  <dc:creator>Poirel, Laurent</dc:creator>
  <dc:date>2019-09-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The plasmid-located mcr-9 gene, encoding a putative phosphoethanolamine  transferase, was identified in a colistin-resistant human fecal Escherichia coli strain  belonging to a very rare phylogroup, the D-ST69-O15:H6 clone. This MCR-9 protein  shares 33% to 65% identity with the other plasmid-encoded MCR-type enzymes  identified (MCR-1 to -8) that have been found as sources of acquired resistance to  polymyxins in Enterobacteriaceae. Analysis of the lipopolysaccharide of the MCR-9- producing isolate revealed a function similar to that of MCR-1 by adding a  phosphoethanolamine group to lipid A and subsequently modifying the structure of the  lipopolysaccharide. However, a minor impact on susceptibility to polymyxins was  noticed once the mcr-9 gene was cloned and produced in an E. coli K-12-derived  strain. Nevertheless, we showed here that subinhibitory concentrations of colistin  induced the expression of the mcr-9 gene, leading to increased MIC levels. This  inducible expression was mediated by a two-component regulatory system encoded  by the qseC and qseB genes located downstream of mcr-9. Genetic analysis showed  that the mcr-9 gene was carried by an IncHI2 plasmid. In silico analysis revealed that  the plasmid-encoded MCR-9 shared significant amino acid identity (ca. 80%) with the  chromosomally encoded MCR-like proteins from Buttiauxella spp. In particular,  Buttiauxella gaviniae was found to harbor a gene encoding MCR-BG, sharing 84%  identity with MCR-9. That gene was neither expressed nor inducible in its original  host, which was fully susceptible to polymyxins. This work showed that mcr genes  may circulate silently and remain undetected unless induced by colistin.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/308225</dc:identifier>
  <dc:identifier>https://sonar.ch/documents/308225/files/nor_mig.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1128/AAC.00965-19</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Antimicrobial Agents and Chemotherapy. - 2019, vol. 63, no. 9, p. 10.1128/aac.00965-19</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">mcr-9, An inducible gene encoding an acquired phosphoethanolamine transferase in Escherichia coli, and its origin</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
