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In vivo development of heterogeneous glycopeptide-intermediate Staphylococcus aureus (hGISA), GISA and daptomycin resistance in a patient with meticillin-resistant S. aureus endocarditis.

Abstract
We report a patient who developed a meticillin-resistant Staphylococcus aureus (MRSA) central venous catheter infection complicated by infective endocarditis. The patient was initially treated with glycopeptides, which led to the development of heterogeneous glycopeptide resistance, the detection of which required the use of a macro Etest screening test. Subsequently, the causative strain, confirmed by PFGE as a UK epidemic MRSA-15, was treated with daptomycin, and again resistance developed in vivo. The development in vivo of resistance to both these agents suggests that the resistance mechanisms may be associated. We suggest that the clinician managing MRSA infection should anticipate daptomycin resistance when reduced glycopeptide susceptibility is detected.
AuthorsAndrew Kirby, Kavya Mohandas, Caroline Broughton, Timothy J Neal, Godfrey W Smith, Pearl Pai, Carlos Nistal de Paz
JournalJournal of medical microbiology (J Med Microbiol) Vol. 58 Issue Pt 3 Pg. 376-380 (Mar 2009) ISSN: 0022-2615 [Print] England
PMID19208891 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Anti-Bacterial Agents
  • Glycopeptides
  • Daptomycin
Topics
  • Adult
  • Anti-Bacterial Agents (pharmacology, therapeutic use)
  • Catheterization, Central Venous (adverse effects)
  • Catheters, Indwelling (microbiology)
  • Daptomycin (pharmacology, therapeutic use)
  • Drug Resistance, Multiple, Bacterial
  • Endocarditis, Bacterial (drug therapy, microbiology)
  • Glycopeptides (pharmacology, therapeutic use)
  • Heart Valve Prosthesis Implantation
  • Humans
  • Male
  • Methicillin-Resistant Staphylococcus aureus (drug effects, isolation & purification)
  • Microbial Sensitivity Tests
  • Mitral Valve (surgery)
  • Renal Dialysis (adverse effects, instrumentation)
  • Renal Insufficiency (complications, therapy)
  • Staphylococcal Infections (drug therapy, microbiology)

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