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Plasmid-Mediated Resistance to Vancomycin and Teicoplanin in Enterococcus Faecium

List of authors.
  • Roland Leclercq, M.D.,
  • Eliane Derlot,
  • Jean Duval, M.D.,
  • and Patrice Courvalin, M.D.

THE glycopeptide antibiotic agents vancomycin and teicoplanin are useful in the treatment of severe infections due to gram-positive bacteria.1 2 3 Staphylococci, streptococci, and enterococci are almost always susceptible to these agents, which constitute an alternative to the penicillins in cases of resistance or intolerance.Resistance to glycopeptides is extremely common in leuconostoc species4 and pediococcus species and also occurs in lactobacilli.5 , 6 These gram-positive bacteria rarely cause infections and are considered opportunistic pathogens. The emergence of strains of Staphylococcus haemolyticus that became resistant during vancomycin therapy has recently been reported.7 Resistance to vancomycin is rare in streptococci.8 Enterococcal isolates with minimal inhibitory . . .

Funding and Disclosures

Presented in part at the 27th Interscience Conference on Antimicrobial Agents and Chemotherapy, New York, October 4–7, 1987.

We are indebted to L. Devriese for help in identification of bacteria and to R. Williamson for determination of penicillin-binding protein patterns. Note added in proof: Since submission of this paper, we have obtained conjugal transfer of plasmid pIP817 to another E. faecium strain.

Author Affiliations

From the Service de Bactériologie–virologic Hygiène, Hôpital Henri Mondor, Université Paris XII, Créteil (R.L., J.D.), and Unité des Agents Antibactériens, Institut Pasteur, Paris (E.D., P.C.), France. Address reprint requests to Dr. Courvalin at the Unité des Agents Antibactériens, Institut Pasteur, 25 Rue du Dr. Roux, 75724 Paris Cedex 15, France.

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