Detection of Vancomycin Resistance among Methicillin-Resistant Staphylococcus aureus Strains Recovered from Children

Lorena Pardo1,2, María Inés Mota1,3, Andrés Parnizari1

  • 1Bacteriology and Virology Academic Unit, Facultad de Medicina, Universidad de la República, Montevideo 11600, Uruguay.

PubMed

Insights

Detecting methicillin-resistant Staphylococcus aureus (MRSA) with decreased vancomycin susceptibility (DSG) is challenging. A rare heterogeneously vancomycin-intermediate Staphylococcus aureus (hVISA) strain was identified in children, emphasizing diagnostic difficulties in clinical microbiology labs.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Clinical Diagnostics

Background:

  • Vancomycin is crucial for treating MRSA infections.
  • Therapeutic failures arise from MRSA with decreased glycopeptide susceptibility (DSG).
  • Early detection of DSG is vital for effective treatment.

Purpose of the Study:

  • To detect and characterize DSG in MRSA from pediatric invasive diseases.
  • To evaluate screening methods for DSG detection.
  • To investigate the prevalence of hVISA in a pediatric hospital setting.

Main Methods:

  • Screening MRSA strains using agar plates (BHI-3, BHI-4), VITEK2, and E-tests.
  • Confirming heterogeneously vancomycin-intermediate Staphylococcus aureus (hVISA) via population analysis profiling-area under the curve (PAP-AUC).
  • Analyzing bacterial cell wall thickness using transmission electron microscopy.

Main Results:

  • No vancomycin-resistant (VRSA) or vancomycin-intermediate (VISA) strains were detected.
  • One MRSA strain (1.9%) was confirmed as hVISA by PAP-AUC.
  • The confirmed hVISA strain, belonging to ST30 with SCCmec IV, exhibited increased cell wall thickness but was missed by initial screening methods.

Conclusions:

  • Heterogeneously vancomycin-intermediate Staphylococcus aureus (hVISA) is rare in pediatric invasive infections.
  • Standard screening methods may fail to detect hVISA.
  • Accurate hVISA detection poses a significant challenge for clinical microbiology laboratories.

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