Multidrug-Resistant Methicillin-Resistant Staphylococcus aureus Associated with Hospitalized Newborn Infants.
Ching Hoong ChewChew Chieng YeoAinal Mardziah Che HamzahEsra'a I Al-TradSherry Usun JonesKek-Heng ChuaSuat Moi PuahPublished in: Diagnostics (Basel, Switzerland) (2023)
Multidrug resistance (MDR) is a significant challenge in healthcare management, and addressing it requires a comprehensive approach. In this study, we employed a combination of phenotypic and genotypic approaches, along with whole genome sequencing (WGS) to investigate five hospital-associated MDR methicillin-resistant Staphylococcus aureus (MRSA) strains that were isolated from newborn infants. Our analysis revealed the following for the MDR-MRSA strains: SauR31 was resistant to three antimicrobial classes; SauR12, SauR91 and SauR110 were resistant to four antimicrobial classes; and SauR23 exhibited resistance to seven classes. All the MDR-MRSA strains were capable of producing slime and biofilms, harbored SCC mec type IV, and belonged to different spa types (t022, t032, and t548), with varying profiles for microbial surface components recognizing adhesive matrix molecules (MSCRAMMs) and virulence genes. The WGS data for the MDR SauR23 and SauR91 strains revealed that most of the antimicrobial resistance genes were present in the chromosomes, including blaZ , mecA , norA , lmrS , and sdrM , with only the ermC gene found in a small (<3 kb) plasmid. The presence of MDR-MRSA strains among neonates raises public concern, hence implementation of multifaceted interventions is recommended to address this issue. In addition, metadata is needed to improve the investigation of antimicrobial resistance genes in MDR isolates.
Keyphrases
- methicillin resistant staphylococcus aureus
- multidrug resistant
- antimicrobial resistance
- staphylococcus aureus
- escherichia coli
- healthcare
- drug resistant
- gram negative
- acinetobacter baumannii
- genome wide
- klebsiella pneumoniae
- genome wide identification
- biofilm formation
- genome wide analysis
- primary care
- microbial community
- electronic health record
- dna methylation
- physical activity
- single cell
- acute care
- social media
- cystic fibrosis
- transcription factor
- health information
- adverse drug