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ClpP-independent function of ClpX interferes with telithromycin resistance conferred by Msr(A) in Staphylococcus aureus.

Vladimir VimbergJakub LenartJiri JanataGabriela Balikova Novotna
Published in: Antimicrobial agents and chemotherapy (2015)
The ABCF family protein Msr(A) confers high resistance to macrolides but only low resistance to ketolides in staphylococci. Mutations in conserved functional regions of ClpX as well as deletion of clpX significantly increased Msr(A)-mediated resistance to the ketolide antibiotic telithromycin. ClpX is the chaperone component of the ClpXP two-component proteolytic system. Nevertheless, no changes in resistance were observed in a clpP knockout strain expressing msr(A), demonstrating that ClpX affects Msr(A) independently of ClpP.
Keyphrases
  • staphylococcus aureus
  • escherichia coli
  • cystic fibrosis
  • small molecule
  • biofilm formation
  • amino acid
  • heat shock protein
  • heat stress
  • protein protein