Fosfomycin resistance mechanisms in Enterobacterales: an increasing threat

Vittoria Mattioni Marchetti1,2,3, Jaroslav Hrabak1,2, Ibrahim Bitar1,2

  • 1Department of Microbiology, Faculty of Medicine, University Hospital in Pilsen, Charles University, Pilsen, Czechia.

Insights

Fosfomycin resistance is rising in Gram-negative bacteria, particularly Enterobacterales, due to altered influx and resistance genes like FosA. Identifying resistance is challenging, impacting treatment options.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background:

  • Antimicrobial resistance (AMR) poses a global health threat, necessitating the re-evaluation of older antibiotics like fosfomycin (FOS).
  • Fosfomycin is regaining clinical interest for treating multi-drug resistant (MDR) bacterial infections.
  • Rising fosfomycin resistance (FOSR) in Gram-negative pathogens, especially Enterobacterales, compromises its effectiveness.

Purpose of the Study:

  • To review the mechanisms of FOS influx into bacterial cells.
  • To investigate mutations affecting FOS effectiveness.
  • To summarize the global epidemiology of FosA/C2/L1-2 enzymes in Enterobacterales.

Main Methods:

  • Literature review of studies on FOS influx mechanisms.
  • Analysis of mutations impacting FOS transport and efficacy.
  • Epidemiological summary of FosA/C2/L1-2 enzyme variants in Enterobacterales.

Main Results:

  • FOS effectiveness is reduced by altered FOS influx or acquired resistance genes.
  • Eleven variants of FosA enzymes have been reported globally.
  • FosA3 is the most prevalent acquired resistance mechanism in Enterobacterales, followed by FosA7 and FosA5.
  • Genes like fosA/C2 are transmitting in high-risk clones (e.g., E. coli ST131, K. pneumoniae ST11).
  • Rapid identification of FOSR in Enterobacterales is hindered by a lack of commercial tests.

Conclusions:

  • Understanding FOS influx mechanisms and resistance gene spread is crucial for combating AMR.
  • Fosfomycin remains valuable, especially in combination therapy, but resistance surveillance is needed.
  • Development of rapid diagnostic tools for FOS resistance is essential for effective clinical management.

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