HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Persistent bacteremia due to methicillin-resistant Staphylococcus aureus infection is associated with agr dysfunction and low-level in vitro resistance to thrombin-induced platelet microbicidal protein.

AbstractBACKGROUND:
The causes of persistent bacteremia (PB) due to methicillin-resistant Staphylococcus aureus (MRSA) are poorly understood. This investigation examined potential associations between PB with key clinical features and several in vitro bacterial genotypic and phenotypic characteristics, in isolates from 1 institution.
METHODS:
Pulsed-field gel electrophoresis (PFGE) relatedness, thrombin-induced platelet microbicidal protein (tPMP)-susceptibility phenotype, accessory gene regulator (agr) genotype and functionality (via delta-lysin production), and autolysis phenotypes were assessed in MRSA isolates from the bloodstream of 21 prospectively identified patients with PB (blood cultures positive after > or =7 days of therapy) and of 18 patients with resolving bacteremia (RB) (sterile blood cultures within the first 2-4 days of therapy) due to MRSA.
RESULTS:
The 2 groups had comparable baseline characteristics but differed in their clinical courses (e.g., endocarditis was more frequent in patients with PB than in those with RB [43% vs. 0%, respectively; P=.0016]); isolates from patients with PB exhibited higher rates of (1) survival in vitro after exposure to tPMP (22.4+/-14.8% vs. 11.6+/-6.5%, respectively; P=.005); (2) defective delta-lysin production (71.4% vs. 38.9%, respectively; P=.057); (3) non-agr genotype II profile (100% vs. 77.8%, respectively; P=.037); and (4) overrepresentation of a specific PFGE genotype (85.7% vs. 44.4%, respectively; P=.015).
CONCLUSIONS:
Isolates from patients with PB differed from those in patients with RB, in several in vitro characteristics. Further studies will be necessary to define how these factors might affect clinical outcome.
AuthorsVance G Fowler Jr, George Sakoulas, Lauren M McIntyre, Venkata G Meka, Robert D Arbeit, Christopher H Cabell, Martin E Stryjewski, George M Eliopoulos, L Barth Reller, G Ralph Corey, Tiffanny Jones, Natalie Lucindo, Michael R Yeaman, Arnold S Bayer
JournalThe Journal of infectious diseases (J Infect Dis) Vol. 190 Issue 6 Pg. 1140-9 (Sep 15 2004) ISSN: 0022-1899 [Print] United States
PMID15319865 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Agr protein, Staphylococcus aureus
  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Chemokines
  • DNA, Bacterial
  • Hemolysin Proteins
  • PPBP protein, human
  • Trans-Activators
  • beta-Thromboglobulin
  • CCCGGG-specific type II deoxyribonucleases
  • Deoxyribonucleases, Type II Site-Specific
Topics
  • Anti-Bacterial Agents (immunology, pharmacology)
  • Bacteremia (immunology, microbiology)
  • Bacterial Proteins (genetics, physiology)
  • Bacterial Typing Techniques
  • Chemokines (immunology, pharmacology)
  • DNA Fingerprinting
  • DNA, Bacterial (analysis, isolation & purification, metabolism)
  • Deoxyribonucleases, Type II Site-Specific (metabolism)
  • Electrophoresis, Gel, Pulsed-Field
  • Female
  • Genotype
  • Hemolysin Proteins (metabolism)
  • Humans
  • Male
  • Methicillin Resistance
  • Phenotype
  • Polymorphism, Restriction Fragment Length
  • Staphylococcal Infections (immunology, microbiology)
  • Staphylococcus aureus (drug effects, genetics, isolation & purification)
  • Trans-Activators (genetics, physiology)
  • beta-Thromboglobulin

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: