Expression of multidrug resistance efflux pump genes in clinical and environmental isolates of Staphylococcus aureus

Christos Kosmidis1, Bryan D Schindler, Pauline L Jacinto

  • 1Department of Medicine, Division of Infectious Diseases, Wayne State University School of Medicine, Detroit, MI 48201, USA.

Insights

Multidrug resistance efflux pump gene overexpression in Staphylococcus aureus varies by time and location, impacting hospital environments. Identifying these strains early is crucial for infection control.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genetics

Background:

  • Multidrug resistance efflux pump (MDR-EP) genes are frequently overexpressed in clinical Staphylococcus aureus isolates.
  • The temporal and geographic variability of MDR-EP gene expression and its role in hospital contamination remain largely unknown.

Purpose of the Study:

  • To investigate the temporal and geographic variability of MDR-EP gene expression in Staphylococcus aureus.
  • To determine the prevalence of MDR-EP overexpressing strains in clinical and environmental settings.
  • To identify associations between MDR-EP gene overexpression, specific clones, and antimicrobial resistance.

Main Methods:

  • Analysis of nearly 700 clinical and 91 environmental Staphylococcus aureus isolates.
  • Determination of ethidium bromide (EtBr) minimum inhibitory concentration (MIC).
  • Quantitative expression analysis of chromosomal MDR-EP genes, qacA/B, and smr.
  • spa typing for norA- and/or mepA-overexpressing strains.

Main Results:

  • MDR-EP gene overexpression demonstrated significant temporal and geographic variation.
  • Overexpressing strains were detected in the hospital environment.
  • Increased norA expression correlated with methicillin resistance and spa type t002, suggesting clonal spread of a specific MRSA clone.
  • Clonal spread was also implicated in mepA-overexpressing, methicillin-susceptible strains with spa type t008.
  • An EtBr MIC ≤12.5 μg/mL showed high specificity (>90%) for identifying strains lacking MDR-EP gene overexpression.

Conclusions:

  • MDR-EP gene expression in Staphylococcus aureus is dynamic and geographically influenced, posing potential infection control challenges.
  • Specific clones, such as a norA-overexpressing MRSA clone (spa type t002) and a mepA-overexpressing MSSA clone (spa type t008), are associated with MDR-EP overexpression.
  • EtBr MIC serves as a reliable indicator for detecting strains with reduced MDR-EP gene expression.

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