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Metabolic remodeling by RNA polymerase gene mutations is associated with reduced β-lactam susceptibility in oxacillin-susceptible MRSA.

Shinya WatanabeChijioke A NsoforKanate ThitiananpakornXin-Ee TanYoshifumi AibaRemi TakenouchiKotaro KigaTeppei SasaharaKazuhiko MiyanagaSrivani VeeranarayananYuzuki ShimamoriAdeline Yeo Syin LianThuy Minh NguyenHuong Minh NguyenOla AlessaGeoffrey Peterkins KumwendaSarangi JayathilakeJastin Edrian Cocuangco RevillezaPriyanka BaranwalYutaro NishikawaFeng-Yu LiTomofumi KawaguchiSowmiya SankaranarayananMahmoud ArbaahYuancheng Zhangnull ManiruzzamanYi LiuHossain SarahJunjie LiTakashi SuganoThi My Duyen HoAnujin BatboldTergel NayanjinLongzhu Cui
Published in: mBio (2024)
mutations caused RNAP transcription dysfunction, leading to an intracellular accumulation of ribonucleotides and precursors of peptidoglycan as well as wall teichoic acid. This, in turn, caused thickening of the cell wall and ultimately resulted in decreased susceptibility to β-lactam in OS-MRSA. These findings provide insights into the mechanisms of antibiotic resistance in OS-MRSA and highlight the importance of continued research in developing effective treatments to combat antibiotic resistance.
Keyphrases
  • cell wall
  • methicillin resistant staphylococcus aureus
  • staphylococcus aureus
  • gram negative
  • oxidative stress
  • sensitive detection
  • living cells
  • single molecule