Mutations in the two component regulator systems PmrAB and PhoPQ give rise to increased colistin resistance in

Matthew E Wand1, J Mark Sutton1

  • 1Public Health England, National Infection Service, Porton Down, Salisbury, Wiltshire, SP4 0JG, UK.

Insights

Colistin resistance can develop in Citrobacter and Enterobacter species with no loss of fitness. However, only certain strains adapt, indicating resistance acquisition depends on individual strain characteristics.

Area of Science:

  • Microbiology
  • Genetics
  • Antimicrobial Resistance

Background:

  • Colistin is a crucial last-resort antibiotic for carbapenem-resistant infections.
  • Mechanisms of colistin resistance are known in Klebsiella pneumoniae and Escherichia coli.
  • Resistance mechanisms in Citrobacter and Enterobacter species remain largely uncharacterized.

Purpose of the Study:

  • To identify mutations causing colistin resistance in Citrobacter and Enterobacter species.
  • To understand the genetic basis of colistin resistance in these Enterobacterales.

Main Methods:

  • Generation of colistin resistance through stepwise or direct exposure to colistin.
  • Whole-genome sequencing to identify resistance-associated mutations.
  • Assessment of growth rate and Galleria mellonella virulence in resistant mutants.

Main Results:

  • Colistin resistance was successfully generated in select Citrobacter and Enterobacter strains, increasing MIC 16-fold.
  • Mutations in PmrB (Citrobacter) and PhoP (Enterobacter) were identified as key drivers of resistance.
  • Resistant mutants exhibited minimal impact on growth rate and virulence, though strain-dependent variations exist.

Conclusions:

  • Stable colistin resistance can be acquired by Citrobacter and Enterobacter without compromising bacterial fitness.
  • The ability to acquire colistin resistance is strain-specific, influenced by inherent genetic characteristics.
  • Further research is needed to fully elucidate resistance mechanisms in all strains.

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