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Antimicrobial Agents and Chemotherapy, March 2009, p. 1260-1263, Vol. 53, No. 3
0066-4804/09/$08.00+0 doi:10.1128/AAC.01453-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

JMI Laboratories, North Liberty, Iowa,1 Women's and Children's Hospital, North Adelaide, Australia2
Received 30 October 2008/ Returned for modification 19 December 2008/ Accepted 26 December 2008
Dalbavancin, a long-acting lipoglycopeptide, was evaluated against 81,673 isolates of staphylococci, enterococci, and streptococci collected from 33 countries during worldwide resistance surveillance (2002 to 2007). Regardless of susceptibility to oxacillin, comparable potencies for dalbavancin against Staphylococcus aureus and coagulase-negative staphylococci from all countries were noted (MIC90, 0.06 to 0.12 µg/ml). Vancomycin-susceptible Enterococcus spp. had dalbavancin MIC90s comparable to those for staphylococci, whereas vancomycin-resistant strains were more resistant (MIC50, >4 µg/ml). β-Hemolytic and viridians group streptococci were very susceptible to dalbavancin (MIC90,
0.03 µg/ml). Overall, dalbavancin was
16-fold more active than vancomycin against the monitored gram-positive species.
Published ahead of print on 5 January 2009.
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