Burden of Rifampicin- and Methicillin-Resistant Staphylococcus aureus in Italy

Dafne Bongiorno1, Gino Mongelli1, Stefania Stefani1

  • 1Medical Molecular Microbiology and Antibiotic Resistance Laboratory (MMAR Lab), Department of Biomedical and Biotechnological Sciences (BIOMETEC), University of Catania , Catania, Italy .

Microbial Drug Resistance (Larchmont, N.Y.)
|November 30, 2017
PubMed

Insights

Rifampicin resistance in MRSA is rising in Italy, linked to specific bacterial clones and mutations. This complex resistance poses a significant challenge for treating infections, even with newer antibiotics.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background:

  • Methicillin-resistant Staphylococcus aureus (MRSA) infections are a significant healthcare concern.
  • Rifampicin is a key antibiotic for MRSA treatment, but rifampicin resistance (RIF-R) is increasing globally.
  • Italy shows a higher prevalence of RIF-R in multidrug-resistant MRSA (16.4%) compared to Europe (5.7%).

Purpose of the Study:

  • To investigate the relationship between bacterial clones, rpoB gene mutations, and antimicrobial susceptibility profiles in RIF-R MRSA isolates from hospitalized patients in Italy.
  • To understand the genetic and phenotypic characteristics of RIF-R MRSA strains.
  • To assess the clinical implications of RIF-R MRSA in a healthcare setting.

Main Methods:

  • Antimicrobial susceptibility testing using broth microdilution.
  • Bacterial isolate characterization via MLST, SCCmec, and spa-typing.
  • Analysis of the rpoB gene through PCR and sequence analysis.

Main Results:

  • RIF-R MRSA isolates exhibited high rates of heterogeneous vancomycin-intermediate S. aureus (hVISA) (60%) and daptomycin nonsusceptibility (22%).
  • Dominant MRSA clones included ST228-SCCmec I (44%), ST8-SCCmec IV (18%), ST239-SCCmec III (16%), ST5-SCCmec II (14%), and ST22-SCCmec IVh (4%).
  • Thirteen distinct RpoB amino acid substitutions were identified, with H481N being common for low-level resistance, while other single or multiple mutations conferred high-level resistance.

Conclusions:

  • The study identified ST228 as a prevalent clone in Italy, strongly associated with reduced susceptibility to glycopeptides (hVISA).
  • The increasing prevalence of RIF-R MRSA strains with complex resistance mechanisms poses a serious threat to patient treatment.
  • These findings highlight the difficulty in treating infections caused by these multidrug-resistant strains, even with novel antibiotics.