E. coli ST11 (O157:H7) does not encode a functional AcrF efflux pump

Hannah L Pugh, Christopher Connor, Pauline Siasat, Alan McNally, Jessica M A Blair*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Escherichia coli is a facultative anaerobe found in a wide range of environments. Commonly described as the laboratory workhorse, E. coli is one of the best characterized bacterial species to date, however much of our understanding comes from studies involving the laboratory strain E. coli K-12. Resistance-nodulation-division efflux pumps are found in Gram-negative bacteria and can export a diverse range of substrates, including antibiotics. E. coli K-12 has six RND pumps; AcrB, AcrD, AcrF, CusA, MdtBC and MdtF, and it is frequently reported that all E. coli strains possess these six pumps. However, this is not true of E. coli ST11, a lineage of E. coli, which is primarily composed of the highly virulent important human pathogen, E. coli O157:H7. Here we show that acrF is absent from the pangenome of ST11 and that this lineage of E. coli has a highly conserved insertion within the acrF gene, which when translated encodes 13 amino acids and two stop codons. This insertion was found to be present in 97.59 % of 1787 ST11 genome assemblies. Non-function of AcrF in ST11 was confirmed in the laboratory as complementation with acrF from ST11 was unable to restore AcrF function in E. coli K-12 substr. MG1655 ΔacrB ΔacrF. This shows that the complement of RND efflux pumps present in laboratory bacterial strains may not reflect the situation in virulent strains of bacterial pathogens.

Original languageEnglish
Article number001324
JournalMicrobiology
Volume169
Issue number4
DOIs
Publication statusPublished - 19 Apr 2023

Keywords

  • Humans
  • Escherichia coli/genetics
  • Membrane Transport Proteins/genetics
  • Anti-Bacterial Agents/pharmacology
  • Escherichia coli Proteins/genetics
  • Multidrug Resistance-Associated Proteins/metabolism
  • Membrane Proteins/metabolism

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