Multidrug-Resistant Methicillin-Resistant Staphylococcus aureus Associated with Hospitalized Newborn Infants

Ching Hoong Chew1, Chew Chieng Yeo2, Ainal Mardziah Che Hamzah1

  • 1Faculty of Health Sciences, Universiti Sultan Zainal Abidin, Kuala Terengganu 21300, Malaysia.

Insights

Multidrug-resistant methicillin-resistant Staphylococcus aureus (MRSA) strains were found in hospital-associated newborn infants. These strains exhibited slime and biofilm production, with resistance genes located primarily on chromosomes.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genomics

Background:

  • Multidrug resistance (MDR) in healthcare settings poses a significant challenge.
  • Methicillin-resistant Staphylococcus aureus (MRSA) is a major cause of hospital-acquired infections.
  • Neonatal intensive care units are particularly vulnerable to MDR pathogen outbreaks.

Purpose of the Study:

  • To investigate the characteristics of hospital-associated MDR-MRSA strains isolated from newborn infants.
  • To determine the antimicrobial resistance profiles, virulence factors, and genetic makeup of these strains.
  • To identify potential sources and transmission routes of MDR-MRSA in neonatal populations.

Main Methods:

  • Phenotypic and genotypic analyses were performed on five MDR-MRSA isolates.
  • Whole genome sequencing (WGS) was utilized to identify antimicrobial resistance genes and genetic elements.
  • Analysis included antimicrobial susceptibility testing, slime and biofilm formation assays, SCCmec typing, spa typing, and virulence gene profiling.

Main Results:

  • All five MDR-MRSA strains produced slime and biofilms and harbored SCCmec type IV.
  • Antimicrobial resistance varied, with one strain resistant to seven classes of antibiotics.
  • WGS revealed that most antimicrobial resistance genes were chromosomally located, with one plasmid-borne gene (ermC).

Conclusions:

  • The presence of MDR-MRSA in neonates is a serious public health concern.
  • Multifaceted interventions are crucial to control the spread of these resistant strains.
  • Improved metadata collection is essential for future antimicrobial resistance investigations.

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