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Vancomycin-resistant Enterococcus faecium: catheter colonization, esp gene, and decreased susceptibility to antibiotics in biofilm.

Abstract
To evaluate the molecular characteristics and antibiotic susceptibility in biofilm of vancomycin-resistant Enterococcus faecium (VREF) organisms that had caused catheter-related VREF bacteremia (VREF-CRB), we compared 22 isolates causing bacteremia obtained from patients with VREF-CRB with 30 isolates from control patients with gastrointestinal colonization by VREF. Using pulsed-field gel electrophoresis, we identified 17 unique strains among the 22 VREF-CRB isolates and 23 strains among the gastrointestinal isolates. The esp gene was detected in 53% (9 of 17) of the VREF-CRB and 61% (14 of 23) of the control strains (P = 0.6). VREF-CRB produced heavier biofilm colonization of silicone disks than did control organisms (P < 0.001). Daptomycin, minocycline, and quinupristin-dalfopristin were each independently more active than linezolid in reducing biofilm colonization by VREF-CRB (P < 0.01), with daptomycin being the most active, followed by minocycline. In conclusion, the esp gene in VREF is not associated with heavy biofilm colonization or catheter-related bacteremia. In biofilm, daptomycin and minocycline were the most active antibiotics against VREF, and linezolid was the least active.
AuthorsIssam I Raad, Hend A Hanna, Maha Boktour, Gassan Chaiban, Ray Y Hachem, Tanya Dvorak, Russell Lewis, Barbara E Murray
JournalAntimicrobial agents and chemotherapy (Antimicrob Agents Chemother) Vol. 49 Issue 12 Pg. 5046-50 (Dec 2005) ISSN: 0066-4804 [Print] United States
PMID16304171 (Publication Type: Journal Article)
Chemical References
  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Membrane Proteins
  • enterococcal surface protein, esp
Topics
  • Anti-Bacterial Agents (pharmacology, therapeutic use)
  • Bacteremia (drug therapy, microbiology)
  • Bacterial Proteins (physiology)
  • Biofilms (growth & development)
  • Catheterization (adverse effects)
  • Enterococcus faecium (drug effects, genetics, pathogenicity)
  • Gastrointestinal Tract (microbiology)
  • Humans
  • Membrane Proteins (physiology)
  • Microbial Sensitivity Tests
  • Vancomycin Resistance (physiology)

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