High diversity in SCCmec elements among multidrug-resistant Staphylococcus haemolyticus strains originating from

Farideh Hosseinkhani1, Matthias Tammes Buirs1, Fereshteh Jabalameli2

  • 1Department of Innovative Molecular Diagnostics, University of Applied Sciences Leiden, Leiden, the Netherlands.

Abstract

Insights

Multidrug-resistant Staphylococcus haemolyticus strains from children show diverse SCCmec types, including a novel composite island. This finding highlights the evolving nature of antimicrobial resistance in this pathogen.

Area of Science:

  • Clinical Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Staphylococcus haemolyticus is a significant healthcare-associated pathogen, particularly in neonatal intensive care units.
  • Increasing antimicrobial resistance in S. haemolyticus poses a threat to vulnerable patient populations.
  • Understanding the genetic basis of this resistance, specifically SCCmec types, is crucial for effective treatment and control.

Purpose of the Study:

  • To investigate the diversity and characteristics of SCCmec types among multidrug-resistant S. haemolyticus (MDR-SH) strains isolated from pediatric patients.
  • To identify novel genetic elements contributing to antimicrobial resistance in these strains.

Main Methods:

  • Isolation and characterization of 60 S. haemolyticus strains from pediatric patients.
  • Antibiotic resistance profiling using disk agar diffusion and micro-broth dilution methods.
  • Whole-genome sequencing (WGS) and PCR analysis for SCCmec typing.

Main Results:

  • All 60 S. haemolyticus isolates exhibited multidrug resistance.
  • WGS revealed diverse SCCmec types, including a novel composite island [SCCmec type V (Vd)+SCC cad/ars/cop] in 30% of strains.
  • SCCmec type V was found in 23% of isolates; 11 strains had an mecA gene complex with IS431 elements and lacked mecRI/ccr genes.

Conclusions:

  • A high degree of SCCmec element diversity was observed in MRSH strains, with a novel composite island being prevalent.
  • The study describes for the first time the structure of this composite island in MDR-SH strains, including a type III restriction-modification system.
  • The findings suggest that the mecA gene complex may integrate as a composite transposon independently of recombinase genes, facilitated by direct repeats.

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