Prevalence and Microbiological Characteristics of qacA/B-Positive Methicillin-Resistant Staphylococcus aureus Isolates in a Surgical Intensive Care Unit

Microb Drug Resist. 2018 Apr;24(3):283-289. doi: 10.1089/mdr.2017.0072. Epub 2017 Aug 11.

Abstract

The increasing use of chlorhexidine for methicillin-resistant Staphylococcus aureus (MRSA) decolonization has raised concerns about the emergence of resistance to or tolerance of this antiseptic. We examined the frequency and characteristics of qacA/B chlorhexidine tolerance genes among MRSA isolates in a surgical intensive care unit (ICU) where MRSA-colonized patients are decolonized by chlorhexidine bathing. The MRSA isolates were evaluated for chlorhexidine susceptibility, mupirocin resistance, molecular typing, agr functionality, and the heterogeneous vancomycin-intermediate S. aureus (hVISA) phenotype according to the presence of the qacA/B genes. Overall, 119 MRSA isolates were obtained from active surveillance cultures (93, 78.2%) and clinical cultures (26, 21.8%) between 2012 and 2014. Among these isolates, 39 (32.8%) carried the qacA/B genes, and 23 (19.3%) exhibited mupirocin resistance. Most qacA/B-positive isolates (36/39, 92.3%) were identified as ST5-SCCmecII (69.2%) and ST239-SCCmecIII (23.1%), which are common healthcare-associated (HA)-MRSA strains in Korea. Multivariate analysis found that qacA/B-positive MRSA isolates were associated with agr dysfunction (OR, 4.87; 95% CI, 1.71-13.87) and the hVISA phenotype (OR, 4.09; 95% CI, 1.48-11.34). In conclusion, our study showed that qacA/B carriage was common among MRSA isolates in an ICU where chlorhexidine is commonly used for decolonization. qacA/B carriage was significantly associated with agr dysfunction and the hVISA phenotype. These features may confer a selective advantage on HA-MRSA strains, including ST5-SCCmecII and ST239-SCCmecIII, in the ICU setting.

Keywords: Staphylococcus aureus; chlorhexidine; microbial drug resistance.

MeSH terms

  • Aged
  • Anti-Infective Agents, Local / pharmacology
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Chlorhexidine / pharmacology
  • Drug Resistance, Multiple, Bacterial / genetics*
  • Female
  • Gene Expression Regulation, Bacterial*
  • Humans
  • Intensive Care Units
  • Male
  • Membrane Transport Proteins / genetics*
  • Membrane Transport Proteins / metabolism
  • Methicillin-Resistant Staphylococcus aureus / classification
  • Methicillin-Resistant Staphylococcus aureus / drug effects
  • Methicillin-Resistant Staphylococcus aureus / genetics*
  • Methicillin-Resistant Staphylococcus aureus / isolation & purification
  • Middle Aged
  • Mupirocin / pharmacology
  • Prevalence
  • Republic of Korea / epidemiology
  • Retrospective Studies
  • Staphylococcal Infections / drug therapy
  • Staphylococcal Infections / epidemiology*
  • Staphylococcal Infections / microbiology
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Vancomycin / pharmacology

Substances

  • Agr protein, Staphylococcus aureus
  • Anti-Infective Agents, Local
  • Bacterial Proteins
  • Membrane Transport Proteins
  • QacB protein, Staphylococcus aureus
  • Trans-Activators
  • qacA protein, Staphylococcus aureus
  • Vancomycin
  • Mupirocin
  • Chlorhexidine