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Practical disk diffusion method for detection of inducible clindamycin resistance in Staphylococcus aureus and

K R Fiebelkorn1, S A Crawford, M L McElmeel

  • 1Department of Pathology, University of Texas Health Science Center, San Antonio, Texas 78229-3750, USA. fiebelkorn@uthscsa.edu

Insights

Standard disk placement reliably detects inducible macrolide-lincosamide-streptogramin B (MLSB) resistance in Staphylococcus strains. This method accurately identifies inducible MLSB resistance in Staphylococcus aureus and coagulase-negative staphylococci (CNS).

Area of Science:

  • Clinical Microbiology
  • Antimicrobial Resistance

Background:

  • Staphylococcal resistance to macrolides arises from active efflux (msrA) or ribosomal target modification (macrolide-lincosamide-streptogramin B [MLSB] resistance; ermA, ermC).
  • MLSB resistance can be constitutive or inducible, with induction detected by observing the flattening of the clindamycin zone adjacent to an erythromycin disk.
  • The reliability of standard disk dispenser distances (26-28 mm) for detecting inducible MLSB resistance requires reassessment.

Purpose of the Study:

  • To evaluate the effectiveness of standard disk approximation (26-28 mm) for detecting inducible MLSB resistance in Staphylococcus aureus and coagulase-negative staphylococci (CNS).
  • To compare the standard disk distance with closer approximations (15 or 20 mm) in identifying inducible resistance.

Main Methods:

  • Disk approximation tests were performed on 130 Staphylococcus aureus and 100 erythromycin-resistant coagulase-negative staphylococci (CNS) isolates.
  • PCR was used to detect ermA, ermC, and msrA genes in CNS isolates and a subset of S. aureus isolates.
  • Inducible resistance was assessed using erythromycin and clindamycin disks placed at standard (26-28 mm) and closer (15, 20 mm) distances.

Main Results:

  • Standard disk placement detected inducible MLSB resistance in 97% of S. aureus and 100% of CNS strains.
  • Only one S. aureus isolate showed unclear induction at the 26 mm distance.
  • No inducible resistance was detected in isolates with only the msrA gene or in erythromycin-susceptible strains.

Conclusions:

  • Simple placement of erythromycin and clindamycin disks using a standard disk dispenser is a reliable method for detecting inducible MLSB resistance in staphylococci.
  • This standard method effectively identifies inducible MLSB resistance in both S. aureus and CNS, simplifying routine laboratory diagnostics.

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