Previous Article | Next Article ![]()
Antimicrobial Agents and Chemotherapy, January 1999, p. 166-168, Vol. 43, No. 1
Department of Pathology, Hershey Medical
Center, Hershey, Pennsylvania 17033,1 and
Department of Pathology, Case Western Reserve University,
Cleveland, Ohio 441062
Received 26 May 1998/Returned for modification 25 August
1998/Accepted 12 October 1998
Agar dilution was used to test the activities of HMR 3647, erythromycin A, azithromycin, clarithromycin, roxithromycin,
clindamycin, and quinupristin-dalfopristin against 235 strains of
Enterococcus faecalis. HMR 3647 was the most active
compound (MICs at which 50 and 90% of the isolates are inhibited
[MIC50 and MIC90, respectively] of 0.06 and
4.0 µg/ml, respectively). The MIC50 and MIC90
(with the MIC50 given first and the MIC90 given
second; both in micrograms per milliliter) for other compounds were as
follows: 4.0 and >32.0 for erythromycin A, 16.0 and >32.0 for
azithromycin, 2.0 and >32 for clarithromycin, 32.0 and >32.0 for
roxithromycin, 32.0 and >32.0 for clindamycin, and 8.0 and 16.0 for
quinupristin-dalfopristin. All compounds were only bacteriostatic.
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Activity of HMR 3647 Compared to Those of Six
Compounds against 235 Strains of Enterococcus
faecalis
*
Corresponding author. Mailing address: Department of
Pathology, Hershey Medical Center, 500 University Dr., Hershey,
PA 17033. Phone: (717) 531-5113. Fax: (717) 531-7953. E-mail:
pappelbaum{at}psghs.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»