Previous Article | Next Article 
Antimicrobial Agents and Chemotherapy, May 2003, p. 1689-1693, Vol. 47, No. 5
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.5.1689-1693.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Baseline Study To Determine In Vitro Activities of Daptomycin against Gram-Positive Pathogens Isolated in the United States in 2000-2001
Ian A. Critchley,1 Renée S. Blosser-Middleton,1 Mark E. Jones,2 Clyde Thornsberry,3 Daniel F. Sahm,1 and James A. Karlowsky1*
Focus Technologies, Inc., Herndon, Virginia,1
Focus Technologies, Hilversum, The Netherlands,2
Focus Technologies, Franklin, Tennessee3
Received 16 August 2002/
Returned for modification 11 February 2003/
Accepted 21 February 2002
The activity of daptomycin was assessed by using 6,973 gram-positive bacteria isolated at 50 United States hospitals in 2000 and 2001. Among the isolates of Streptococcus pneumoniae (n = 1,163) collected, the rate of penicillin resistance was 16.1%; rates of oxacillin resistance among Staphylococcus aureus isolates (n = 1,018) and vancomycin resistance among Enterococcus faecium isolates (n = 368) were 30.0 and 59.5%, respectively. Multidrug-resistant (MDR) phenotypes (isolates resistant to three or more different chemical classes of antimicrobial agents) accounted for 14.2% of S. pneumoniae isolates, 27.1% of S. aureus isolates, and 58.4% of E. faecium isolates. For all gram-positive species tested, MICs at which 90% of the isolates tested were inhibited (MIC90s) and MIC ranges for directed-spectrum agents (daptomycin, quinupristin-dalfopristin, and linezolid) were identical or highly similar for isolates susceptible or resistant to other agents or MDR. Daptomycin had a MIC90 of 0.12 µg/ml for both penicillin-susceptible and -resistant isolates of S. pneumoniae. Against oxacillin-resistant S. aureus daptomycin had a MIC90 of 0.5 µg/ml, and it had a MIC90 of 4 µg/ml against both vancomycin-susceptible and -resistant E. faecium. The MIC90s for daptomycin and other directed-spectrum agents were unaffected by the regional or anatomical origin of isolates or patient demographic parameters (patient age, gender, and inpatient or outpatient care). Our results confirm the gram-positive spectrum of activity of daptomycin and that its activity is independent of susceptibility or resistance to commonly prescribed and tested antimicrobial agents. This study may serve as a baseline to monitor future changes in the susceptibility of gram-positive species to daptomycin following its introduction into clinical use.
* Corresponding author. Mailing address: Focus Technologies, Inc., 13665 Dulles Technology Dr., Suite 200, Herndon, VA 20171. Phone: (703) 480-2500. Fax: (703) 480-2670. E-mail:
jkarlowsky{at}focusanswers.com.
Antimicrobial Agents and Chemotherapy, May 2003, p. 1689-1693, Vol. 47, No. 5
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.5.1689-1693.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Hidron, A. I., Schuetz, A. N., Nolte, F. S., Gould, C. V., Osborn, M. K.
(2008). Daptomycin resistance in Enterococcus faecalis prosthetic valve endocarditis. J Antimicrob Chemother
61: 1394-1396
[Full Text]
-
Cox, L. A. Jr., Popken, D. A., Carnevale, R.
(2007). Quantifying Human Health Risks from Animal Antimicrobials. Interfaces
37: 22-38
[Abstract]
-
French, G. L.
(2006). Bactericidal agents in the treatment of MRSA infections--the potential role of daptomycin. J Antimicrob Chemother
58: 1107-1117
[Abstract]
[Full Text]
-
Fowler, V. G. Jr., Boucher, H. W., Corey, G. R., Abrutyn, E., Karchmer, A. W., Rupp, M. E., Levine, D. P., Chambers, H. F., Tally, F. P., Vigliani, G. A., Cabell, C. H., Link, A. S., DeMeyer, I., Filler, S. G., Zervos, M., Cook, P., Parsonnet, J., Bernstein, J. M., Price, C. S., Forrest, G. N., Fatkenheuer, G., Gareca, M., Rehm, S. J., Brodt, H. R., Tice, A., Cosgrove, S. E., the S. aureus Endocarditis and Bacteremia Study Gr,
(2006). Daptomycin versus Standard Therapy for Bacteremia and Endocarditis Caused by Staphylococcus aureus.. NEJM
355: 653-665
[Abstract]
[Full Text]
-
D'Costa, V. M., McGrann, K. M., Hughes, D. W., Wright, G. D.
(2006). Sampling the Antibiotic Resistome. Science
311: 374-377
[Abstract]
[Full Text]
-
Pankey, G., Ashcraft, D., Patel, N.
(2005). In Vitro Synergy of Daptomycin plus Rifampin against Enterococcus faecium Resistant to both Linezolid and Vancomycin. Antimicrob. Agents Chemother.
49: 5166-5168
[Abstract]
[Full Text]
-
Schriever, C. A., Fernandez, C., Rodvold, K. A., Danziger, L. H.
(2005). Daptomycin: A novel cyclic lipopeptide antimicrobial. Am J Health Syst Pharm
62: 1145-1158
[Abstract]
[Full Text]
-
Streit, J. M., Steenbergen, J. N., Thorne, G. M., Alder, J., Jones, R. N.
(2005). Daptomycin tested against 915 bloodstream isolates of viridans group streptococci (eight species) and Streptococcus bovis. J Antimicrob Chemother
55: 574-578
[Abstract]
[Full Text]
-
Novais, C., Sousa, J. C., Coque, T. M., Peixe, L. V., on behalf of the Portuguese Resistance Study Group,
(2004). In vitro activity of daptomycin against enterococci from nosocomial and community environments in Portugal. J Antimicrob Chemother
54: 964-966
[Full Text]
-
Streit, J. M., Jones, R. N., Sader, H. S.
(2004). Daptomycin activity and spectrum: a worldwide sample of 6737 clinical Gram-positive organisms. J Antimicrob Chemother
53: 669-674
[Abstract]
[Full Text]