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Occurrence of cfr -Positive Linezolid-Susceptible Staphylococcus aureus and Non- aureus Staphylococcal Isolates from Pig Farms.

Gi Yong LeeSoo Jin Yang
Published in: Antibiotics (Basel, Switzerland) (2023)
The emergence and spread of cfr -mediated resistance to linezolid in staphylococci have become a serious global concern. The acquisition of cfr confers multidrug resistance to phenicols, lincosamides, oxazolidinones, pleuromutilins, and streptogramin A (PhLOPS A phenotype). However, occurrence of cfr -positive and linezolid-susceptible staphylococci has been identified. To investigate the mechanism underlying linezolid susceptibility in cfr -positive Staphylococcus aureus and non- aureus staphylococci (NAS) isolates from pig farms in Korea. Eleven cfr -positive and linezolid-susceptible staphylococci were analyzed for mutations in domain V of 23S rRNA, ribosomal proteins (L3, L4, and L22), cfr open reading frames (ORFs), and cfr promoter regions. The effect of the cfr mutation (Q148K) on the PhLOPS A phenotype was determined using plasmid constructs expressing either the mutated ( cfr Q148K ) or nonmutated cfr genes. All 11 (six S. aureus and five NAS) cfr -positive and linezolid-susceptible isolates had a point mutation at position 442 in cfr ORFs (C to A) that resulted in the Q148K mutation. No mutations were detected in 23S rRNA, L3, L4, or L22. The Q148K mutation in Cfr is responsible for phenotypes susceptible to PhLOPS A antimicrobial agents. To our knowledge, this is the first study to report the causal role of a single nucleotide mutation (Q148K) in cfr of S. aureus and NAS isolates in PhLOPS A resistance. Continued nationwide surveillance is necessary to monitor the occurrence and dissemination of mutations in cfr that affect resistance phenotypes in staphylococci of human and animal origin.
Keyphrases
  • staphylococcus aureus
  • methicillin resistant staphylococcus aureus
  • risk assessment
  • healthcare
  • gene expression
  • escherichia coli
  • public health
  • endothelial cells
  • crispr cas
  • cystic fibrosis