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Published on: July 7, 2020
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.
Abstract:
Introduction. Colistin is a last resort antibiotic for treating infections caused by carbapenem-resistant isolates. Mechanisms of resistance to colistin have been widely described in Klebsiella pneumoniae and Escherichia coli but have yet to be characterized in Citrobacter and Enterobacter species.Aim. To identify the causative mutations leading to generation of colistin resistance in Citrobacter and Enterobacter spp.Methodology. Colistin resistance was generated by culturing in increasing concentrations of colistin or by direct culture in a lethal (above MIC) concentration. Whole-genome sequencing was used to identify mutations. Fitness of resistant strains was determined by changes in growth rate, and virulence in Galleria mellonella.Results. We were able to generate colistin resistance upon exposure to sub-MIC levels of colistin, in several but not all strains of Citrobacter and Enterobacter resulting in a 16-fold increase in colistin MIC values for both species. The same individual strains also developed resistance to colistin after a single exposure at 10× MIC, with a similar increase in MIC. Genetic analysis revealed that this increased resistance was attributed to mutations in PmrB for Citrobacter and PhoP in Enterobacter, although we were not able to identify causative mutations in all strains. Colistin-resistant mutants showed little difference in growth rate, and virulence in G. mellonella, although there were strain-to-strain differences.Conclusions. Stable colistin resistance may be acquired with no loss of fitness in these species. However, only select strains were able to adapt suggesting that acquisition of colistin resistance is dependent upon individual strain characteristics.
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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