Potential unreliability of nitrofurantoin disks in susceptibility testing

Insights

Variations in nitrofurantoin disk diffusion tests can lead to inaccurate antimicrobial susceptibility results for Proteus mirabilis. Higher pH in some disks caused falsely larger inhibition zones, misclassifying bacteria as sensitive.

Area of Science:

  • Microbiology
  • Clinical Diagnostics
  • Antimicrobial Resistance

Background:

  • The Kirby-Bauer disk diffusion method is a standard for antimicrobial susceptibility testing (AST).
  • Accurate AST is crucial for guiding antibiotic therapy and combating antimicrobial resistance.
  • Nitrofurantoin is a key antibiotic for treating urinary tract infections, often caused by Proteus species.

Purpose of the Study:

  • To evaluate lot-to-lot variability in commercial nitrofurantoin disks used in Kirby-Bauer testing.
  • To investigate the cause of discrepancies in zone diameters observed with different nitrofurantoin disk lots.
  • To assess the impact of disk variability on the accurate susceptibility categorization of Proteus mirabilis.

Main Methods:

  • Utilized 50 strains of Proteus mirabilis for susceptibility testing.
  • Employed three distinct lots of commercial nitrofurantoin disks.
  • Measured zone diameters and analyzed antimicrobial content and eluate pH for each disk lot.

Main Results:

  • One lot of nitrofurantoin disks produced zone diameters 3–6 mm larger than the other two lots.
  • This discrepancy led to a significant number of Proteus mirabilis strains being incorrectly classified as susceptible.
  • Differences in antimicrobial content did not explain the observed variability; higher eluate pH from the unreliable disks correlated with larger zones.

Conclusions:

  • Lot variability in nitrofurantoin disks can compromise the accuracy of Kirby-Bauer antimicrobial susceptibility testing.
  • Higher eluate pH from certain disk lots promotes faster nitrofurantoin diffusion, leading to erroneously large inhibition zones.
  • Standardization of nitrofurantoin disk manufacturing is essential to ensure reliable AST results and appropriate patient treatment.