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Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 2004 Apr;48(4):1384–1396. doi: 10.1128/AAC.48.4.1384-1396.2004

In Vitro Antimicrobial Activity of Doripenem, a New Carbapenem

Yigong Ge 1, Matthew A Wikler 1, Daniel F Sahm 2, Renée S Blosser-Middleton 2, James A Karlowsky 2,*
PMCID: PMC375337  PMID: 15047550

Abstract

The doripenem MICs at which 90% of the tested strains were inhibited ranged from 0.03 to 1 μg/ml for 10 species of Enterobacteriaceae (n = 351), from 0.03 to 0.12 μg/ml for oxacillin-susceptible staphylococci (n = 119), from 4 to 32 μg/ml for oxacillin-resistant staphylococci (n = 64), from ≤0.008 to 0.06 μg/ml for penicillin-susceptible streptococci (n = 132), and from 1 to 4 μg/ml for penicillin-resistant streptococci (n = 51). Overall, doripenem demonstrated in vitro activity similar to that of meropenem against gram-negative pathogens and to that of imipenem against gram-positive pathogens.


The synthesis of new carbapenems remains an area of intense research because of the broad-spectrum antibacterial activity of this chemical class (6-9, 11, 12). Doripenem (formerly S-4661) is an investigational parenteral 1β-methlycarbapenem, originally discovered by Shionogi & Co., Ltd. (Osaka, Japan) (1), that is currently being developed in the United States by Peninsula Pharmaceuticals, Inc. (Alameda, Calif.) for the treatment of hospitalized patients with serious systemic bacterial infections. Preliminary reports indicate that doripenem has activity against a broad spectrum of bacterial pathogens (6, 9, 11; R. N. Jones, H. Huynh, and D. J. Biedenbach, Abstr. 43rd Intersci. Conf. Antimicrob. Agents Chemother., abstr. F-527, 2003), that it has favorable pharmacokinetic properties (K. Shiba, M. Nakashima, H. Tanimura, H. Okada, J. Shimada, Abstr. 37th Intersci. Conf. Antimicrob. Agents Chemother., abstr. F-217, 1997; D. A. Thye, T. Kilfoil, A. Leighton, and M. Wikler, Abstr. 43rd Intersci. Conf. Antimicrob. Agents Chemother., abstr. A-21, 2003), that it is safe and well tolerated in humans (D. A. Thye et al., 43rd ICAAC), that it is not hydrolyzed by renal dehydropeptidase I like imipenem (2), and that it does not promote the release of endotoxin (10). The objectives of the present study were to investigate the in vitro activity of doripenem against a collection of clinically relevant gram-negative and gram-positive pathogens and to compare the activity of doripenem with the activities of other carbapenems, broad-spectrum cephalosporins, and piperacillin-tazobactam.

(Part of this research was presented at the 43rd Interscience Conference on Antimicrobial Agents and Chemotherapy, Chicago, Ill., 14 to 17 September 2003.)

Isolates tested in the present study were selected from the isolate repository maintained by Focus Technologies (Herndon, Va.) based upon the isolates' species or group identity and their antimicrobial susceptibility testing phenotype; isolates were chosen irrespective of the age of the patient (<1 to 98 years), the specimen source (respiratory, wound, urine, or blood) from which they were isolated, or any other patient demographic parameter. All isolates tested in the present study were collected in U.S. clinical microbiology laboratories from 1999 to 2003. In total, 815 isolates were tested, of which 381 were gram-negative isolates and 434 were gram-positive isolates. Each isolate was taken from frozen stock (−70°C) and subcultured twice onto sheep blood agar; the identity of each isolate was confirmed by using standard clinical laboratory methods applicable to each species or organism group (3).

Antimicrobial susceptibility testing was performed in accordance with the recommended procedures of the National Committee for Clinical Laboratory Standards (NCCLS) (4) by using frozen broth microdilution panels prepared by TREK Diagnostics (Cleveland, Ohio). All isolates were tested against cefepime, ceftriaxone, doripenem, ertapenem, imipenem, meropenem, and piperacillin-tazobactam. Additional antimicrobial agents were tested to confirm antimicrobial susceptibility testing phenotypes and for reference. These agents varied with bacterial species or organism group as follows: gram-negative bacteria were also tested against ampicillin, amoxicillin-clavulanate, aztreonam, ceftazidime, and ciprofloxacin; staphylococci and enterococci were also tested against oxacillin, levofloxacin, and vancomycin; and streptococci were also tested against penicillin, azithromycin, and levofloxacin. Isolates were defined as susceptible, intermediate, or resistant to antimicrobial agents according to NCCLS standard M100-S13 (5). Extended-spectrum β-lactamase (ESBL) confirmatory testing was performed by using the NCCLS recommended method for isolates of Escherichia coli, Klebsiella pneumoniae, and Klebsiella oxytoca (5).

The doripenem MICs at which 90% of the strains were inhibited (MIC90) ranged from 0.03 to 0.5 μg/ml for all Enterobacteriaceae tested, with the exception of Proteus mirabilis (MIC90, 1 μg/ml) (Table 1). The MICs of doripenem for the isolates of Enterobacteriaceae tested were similar to the MICs of ertapenem and meropenem, while imipenem MICs were approximately 2 to 4 doubling dilutions higher than the MICs of the other three carbapenems (Fig. 1). The MICs at which 50% of the strains were inhibited, MIC90s, modal MICs, and MIC ranges of doripenem for ESBL-negative and ESBL-positive E. coli and K. pneumoniae were similar; the MICs of doripenem for ceftazidime-intermediate and -resistant isolates of other Enterobacteriaceae were identical or 1 to 2 doubling dilutions higher than for ceftazidime-susceptible isolates. Generally, the differences in the MICs of ertapenem for ceftazidime-susceptible and ceftazidime-intermediate and -resistant isolates of Enterobacteriaceae were greater (2 to 6 doubling dilutions for all species tested except Providencia spp.) than the differences in those of doripenem, imipenem, and meropenem (Table 1). Against the isolates of Acinetobacter baumannii tested, doripenem demonstrated better activity against ceftazidime-susceptible isolates (MIC90, 1 μg/ml) than against ceftazidime-intermediate and -resistant isolates (MIC90, >16 μg/ml).

TABLE 1.

In vitro MICs of doripenem and comparative β-lactams for A. baumannii, 10 species of Enterobacteriaeae, enterococci, staphylococci, and streptococcia

Organism, antimicrobial agent, and isolate phenotype No. of isolates tested MIC (μg/ml)
Range Mode MIC50 MIC90
Acinetobacter baumannii
    Aztreonam
        Ceftazidime-susceptible 20 8->32 16 32 >32
        Ceftazidime-intermediate or resistant 10 16->32 >32 >32 >32
    Cefepime
        Ceftazidime-susceptible 20 ≤0.5-16 4 4 8
        Ceftazidime-intermediate or resistant 10 8->32 >32 >32 >32
    Ceftriaxone
        Ceftazidime-susceptible 20 4-32 16 16 32
        Ceftazidime-intermediate or resistant 10 32->64 >64 >64 >64
    Doripenem
        Ceftazidime-susceptible 20 0.12-1 0.12 0.25 1
        Ceftazidime-intermediate or resistant 10 0.25->16 1 1 >16
    Ertapenem
        Ceftazidime-susceptible 20 0.5-16 2 2 8
        Ceftazidime-intermediate or resistant 10 2->16 8 8 >16
    Imipenem
        Ceftazidime-susceptible 20 0.06-0.5 0.25 0.25 0.25
        Ceftazidime-intermediate or resistant 10 0.25->16 1 1 8
    Meropenem
        Ceftazidime-susceptible 20 0.12-2 0.25 0.25 1
        Ceftazidime-intermediate or resistant 10 0.25->16 2 2 16
    Piperacillin-tazobactam
        Ceftazidime-susceptible 20 ≤1-32 ≤1 4 32
        Ceftazidime-intermediate or resistant 10 32->128 >128 128 >128
Citrobacter freundii
    Aztreonam
        Ceftazidime-susceptible 21 ≤1-8 ≤1 ≤1 ≤1
        Ceftazidime-intermediate or resistant 20 4->32 16 16 >32
    Cefepime
        Ceftazidime-susceptible 21 ≤0.5 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 20 ≤0.5-16 ≤0.5 1 4
    Ceftriaxone
        Ceftazidime-susceptible 21 ≤0.5-2 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 20 8->64 32 32 >64
    Doripenem
        Ceftazidime-susceptible 21 ≤0.015-0.06 0.03 0.03 0.03
        Ceftazidime-intermediate or resistant 20 0.03-0.25 0.06 0.06 0.12
    Ertapenem
        Ceftazidime-susceptible 21 ≤0.015-0.03 ≤0.015 ≤0.015 ≤0.015
        Ceftazidime-intermediate or resistant 20 0.03-0.5 0.12 0.12 0.5
    Imipenem
        Ceftazidime-susceptible 21 0.12-1 1 1 1
        Ceftazidime-intermediate or resistant 20 0.5-2 0.5 0.5 1
    Meropenem
        Ceftazidime-susceptible 21 ≤0.015-0.03 ≤0.015 ≤0.015 0.03
        Ceftazidime-intermediate or resistant 20 ≤0.015-0.12 0.06 0.06 0.06
    Piperacillin-tazobactam
        Ceftazidime-susceptible 21 ≤1-8 ≤1 ≤1 4
        Ceftazidime-intermediate or resistant 20 4->128 128 64 >128/PICK>
Enterobacter aerogenes
    Aztreonam
        Ceftazidime-susceptible 23 ≤1-8 ≤1 ≤1 2
        Ceftazidime-intermediate or resistant 20 8->32 16 16 >32
    Cefepime
        Ceftazidime-susceptible 23 ≤0.5-1 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 20 ≤0.5->32 ≤0.5 ≤0.5 4
    Ceftriaxone
        Ceftazidime-susceptible 23 ≤0.5-4 ≤0.5 ≤0.5 1
        Ceftazidime-intermediate or resistant 20 4->64 32 32 >64
    Doripenem
        Ceftazidime-susceptible 23 0.03-0.12 0.06 0.06 0.12
        Ceftazidime-intermediate or resistant 20 0.06-0.12 0.12 0.12 0.12
    Ertapenem
        Ceftazidime-susceptible 23 ≤0.015-0.25 ≤0.015 ≤0.015 0.06
        Ceftazidime-intermediate or resistant 20 0.06-1 0.12 0.25 0.5
    Imipenem
        Ceftazidime-susceptible 23 0.5-2 2 2 2
        Ceftazidime-intermediate or resistant 20 0.5-2 0.5 0.5 1
    Meropenem
        Ceftazidime-susceptible 23 ≤0.015-0.06 0.03 0.03 0.06
        Ceftazidime-intermediate or resistant 20 0.03-0.12 0.06 0.06 0.12
    Piperacillin-tazobactam
        Ceftazidime-susceptible 23 ≤1-32 2 2 4
        Ceftazidime-intermediate or resistant 20 16->128 64 64 >128
Enterobacter cloacae
    Aztreonam
        Ceftazidime-susceptible 23 ≤1-8 ≤1 ≤1 2
        Ceftazidime-intermediate or resistant 19 16->32 >32 >32 >32
    Cefepime
        Ceftazidime-susceptible 23 ≤0.5 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 19 ≤0.5-16 1 2 8
    Ceftriaxone
        Ceftazidime-susceptible 23 ≤0.5-4 ≤0.5 ≤0.5 1
        Ceftazidime-intermediate or resistant 19 16->64 >64 >64 >64
    Doripenem
        Ceftazidime-susceptible 23 0.03-0.12 0.03 0.03 0.06
        Ceftazidime-intermediate or resistant 19 0.06-0.25 0.12 0.12 0.25
    Ertapenem
        Ceftazidime-susceptible 23 ≤0.015-0.5 ≤0.015 ≤0.015 0.06
        Ceftazidime-intermediate or resistant 19 0.06-1 0.5 0.5 1
    Imipenem
        Ceftazidime-susceptible 23 0.06-4 0.5 0.5 2
        Ceftazidime-intermediate or resistant 19 0.5-2 0.5 0.5 1
    Meropenem
        Ceftazidime-susceptible 23 ≤0.015-0.25 0.03 0.03 0.06
        Ceftazidime-intermediate or resistant 19 0.06-0.25 0.06 0.06 0.25
    Piperacillin-tazobactam
        Ceftazidime-susceptible 23 ≤1-16 2 2 8
        Ceftazidime-intermediate or resistant 19 8->128 128 128 >128
Escherichia coli
    Aztreonam
        ESBL-negative 22 ≤1-8 ≤1 ≤1 ≤1
        ESBL-positive 18 4->32 >32 >32 >32
    Cefepime
    Ertapenem
        ESBL-negative 20 ≤0.015-0.25 ≤0.015 ≤0.015 ≤0.015
        ESBL-positive 20 ≤0.015-0.5 0.12 0.06 0.25
    Imipenem
        ESBL-negative 20 0.12-1 0.25 0.25 1
        ESBL-positive 20 0.06-1 0.5 0.5 1
    Meropenem
        ESBL-negative 20 ≤0.015-0.25 0.03 0.03 0.03
        ESBL-positive 20 ≤0.015-0.12 0.06 0.03 0.06
    Piperacillin-tazobactam
        ESBL-negative 20 ≤1-8 2 2 4
        ESBL-positive 20 4->128 >128 >128 >128
Morganella morganii
    Aztreonam
        Ceftazidime-susceptible 20 ≤1 ≤1 ≤1 ≤1
        Ceftazidime-intermediate or resistant 1 2
    Cefepime
        Ceftazidime-susceptible 20 ≤0.5-1 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 1 ≤0.5
    Ceftriaxone
        Ceftazidime-susceptible 20 ≤0.5 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 1 ≤0.5
    Doripenem
        Ceftazidime-susceptible 20 0.06-0.5 0.25 0.25 0.5
        Ceftazidime-intermediate or resistant 1 0.5
    Ertapenem
        Ceftazidime-susceptible 20 ≤0.015-0.06 ≤0.015 ≤0.015 0.03
        Ceftazidime-intermediate or resistant 1 0.06
    Imipenem
        Ceftazidime-susceptible 20 0.5-4 4 4 4
        Ceftazidime-intermediate or resistant 1 4
    Meropenem
        Ceftazidime-susceptible 20 0.03-0.25 0.12 0.06 0.12
        Ceftazidime-intermediate or resistant 1 0.12
    Piperacillin-tazobactam
        Ceftazidime-susceptible 20 ≤1-4 ≤1 ≤1 ≤1
        Ceftazidime-intermediate or resistant 1 32
Proteus mirabilis
    Aztreonam
        Ceftazidime-susceptible 22 ≤1->32 ≤1 ≤1 ≤1
        Ceftazidime-intermediate or resistant 19 ≤1->32 >32 >32 >32
    Cefepime
        Ceftazidime-susceptible 22 ≤0.5 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 19 ≤0.5->32 >32 >32 >32
    Ceftriaxone
        Ceftazidime-susceptible 22 ≤0.5 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 19 ≤0.5->64 ≤0.5 8 64
    Doripenem
        Ceftazidime-susceptible 22 0.12-2 0.25 0.5 1
        Ceftazidime-intermediate or resistant 19 0.25-2 1 1 2
    Ertapenem
        Ceftazidime-susceptible 22 ≤0.015-0.25 ≤0.015 ≤0.015 0.06
        Ceftazidime-intermediate or resistant 19 ≤0.015-0.5 0.06 0.06 0.5
    Imipenem
        Ceftazidime-susceptible 22 1-4 4 4 4
        Ceftazidime-intermediate or resistant 19 4-8 4 4 8
    Meropenem
        Ceftazidime-susceptible 22 0.03-0.25 0.06 0.06 0.25
        Ceftazidime-intermediate or resistant 19 0.06-0.25 0.12 0.12 0.25
    Piperacillin-tazobactam
        Ceftazidime-susceptible 22 ≤1-2 ≤1 ≤1 ≤1
        Ceftazidime-intermediate or resistant 19 ≤1-4 ≤1 ≤1 2
Providencia spp.
    Aztreonam
        Ceftazidime-susceptible 20 ≤1-2 ≤1 ≤1 ≤1
        Ceftazidime-intermediate or resistant 3 ≤1-16
    Cefepime
        Ceftazidime-susceptible 20 ≤0.5-2 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 3 ≤0.5-2
    Ceftriaxone
        Ceftazidime-susceptible 20 ≤0.5-2 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 3 ≤0.5-8
    Doripenem
        Ceftazidime-susceptible 20 0.12-0.5 0.25 0.25 0.5
        Ceftazidime-intermediate or resistant 3 0.25
    Ertapenem
        Ceftazidime-susceptible 20 ≤0.015-0.12 ≤0.015 ≤0.015 0.06
        Ceftazidime-intermediate or resistant 3 ≤0.015-0.03
    Imipenem
        Ceftazidime-susceptible 20 0.5-4 2 2 2
        Ceftazidime-intermediate or resistant 3 1-4
    Meropenem
        Ceftazidime-susceptible 20 0.03-0.12 0.06 0.06 0.12
        Ceftazidime-intermediate or resistant 3 0.06-0.12
    Piperacillin-tazobactam
        Ceftazidime-susceptible 20 ≤1-16 ≤1 ≤1 4
        Ceftazidime-intermediate or resistant 3 2-8
Serratia marcescens
    Aztreonam
        Ceftazidime-susceptible 21 ≤1->32 ≤1 ≤1 ≤1
        Ceftazidime-intermediate or resistant 19 2->32 >32 >32 >32
    Cefepime
        Ceftazidime-susceptible 21 ≤0.5-2 ≤0.5 ≤0.5 ≤0.5
        Ceftazidime-intermediate or resistant 19 1->32 32 8 >32
    Ceftriaxone
        Ceftazidime-susceptible 21 ≤0.5-64 ≤0.5 ≤0.5 2
        Ceftazidime-intermediate or resistant 19 4->64 >64 >64 >64
    Doripenem
        Ceftazidime-susceptible 21 0.06-0.5 0.12 0.12 0.25
        Ceftazidime-intermediate or resistant 19 0.12-0.25 0.12 0.12 0.25
    Ertapenem
        Ceftazidime-susceptible 21 ≤0.015-0.25 ≤0.015 0.03 0.12
        Ceftazidime-intermediate or resistant 19 ≤0.015-0.5 0.12 0.12 0.5
    Imipenem
        Ceftazidime-susceptible 21 0.25-4 1 1 2
        Ceftazidime-intermediate or resistant 19 0.5-4 1 1 2
    Meropenem
        Ceftazidime-susceptible 21 0.03-0.12 0.06 0.06 0.06
        Ceftazidime-intermediate or resistant 19 0.03-0.12 0.06 0.06 0.12
    Piperacillin-tazobactam
        Ceftazidime-susceptible 21 ≤1-16 2 2 4
        Ceftazidime-intermediate or resistant 19 4->128 >128 16 >128
Enterococcus faecalis
    Cefepime
        Vancomycin-susceptible 11 32->32 >32 >32 >32
        Vancomycin-intermediate 2 >32
        Vancomycin-resistant 7 32->32
    Ceftriaxone
        Vancomycin-susceptible 11 >64 >64 >64 >64
        Vancomycin-intermediate 2 >64
        Vancomycin-resistant 7 >64
    Doripenem
        Vancomycin-susceptible 11 1-8 8 4 8
        Vancomycin-intermediate 2 4
        Vancomycin-resistant 7 2-8
    Ertapenem
        Vancomycin-susceptible 11 4-32 8 8 16
        Vancomycin-intermediate 2 8-16
        Vancomycin-resistant 7 4-32
    Imipenem
        Vancomycin-susceptible 11 1-2 1 1 2
        Vancomycin-intermediate 2 1-2
        Vancomycin-resistant 7 1-4
    Meropenem
        Vancomycin-susceptible 11 2-32 8 8 16
        Vancomycin-intermediate 2 8
        Vancomycin-resistant 7 2-16
    Piperacillin-tazobactam
        Vancomycin-susceptible 11 2-4 4 4 4
        Vancomycin-intermediate 2 2
        Vancomycin-resistant 7 ≤1-4
Enterococcus faecium
    Cefepime
        Vancomycin-susceptible 10 >32 >32 >32 >32
        Vancomycin-resistant 11 >32 >32 >32 >32
    Ceftriaxone
        Vancomycin-susceptible 10 16->64 >64 >64 >64
        Vancomycin-resistant 11 >64 >64 >64 >64
    Doripenem
        Vancomycin-susceptible 10 2->32 >32 32 >32
        Vancomycin-resistant 11 >32 >32 >32 >32
    Ertapenem
        Vancomycin-susceptible 10 16->32 >32 >32 >32
        Vancomycin-resistant 11 >32 >32 >32 >32
    Imipenem
        Vancomycin-susceptible 10 2->32 >32 16 >32
        Vancomycin-resistant 11 >32 >32 >32 >32
    Meropenem
        Vancomycin-susceptible 10 4->32 >32 >32 >32
        Vancomycin-resistant 11 >32 >32 >32 >32
    Piperacillin-tazobactam
        Vancomycin-susceptible 10 4->64 >64 >64 >64
        Vancomycin-resistant 11 64->64 >64 >64 >64
Staphylococcus aureus
    Cefepime
        Oxacillin-susceptible 42 2-4 2 2 4
        Oxacillin-resistant 23 8->32 >32 >32 >32
    Ceftriaxone
        Oxacillin-susceptible 42 ≤1-4 2 2 4
        Oxacillin-resistant 23 16->64 >64 >64 >64
    Doripenem
        Oxacillin-susceptible 42 ≤0.015-0.06 0.03 0.03 0.06
        Oxacillin-resistant 23 0.25->32 32 4 32
    Ertapenem
        Oxacillin-susceptible 42 0.06-0.25 0.12 0.12 0.25
        Oxacillin-resistant 23 0.5->32 >32 8 >32
    Imipenem
        Oxacillin-susceptible 42 ≤0.015-0.03 0.03 ≤0.015 0.03
        Oxacillin-resistant 23 0.06->32 >32 1 >32
    Meropenem
        Oxacillin-susceptible 42 0.03-0.25 0.06 0.06 0.12
        Oxacillin-resistant 23 0.5->32 >32 4 >32
    Piperacillin-tazobactam
        Oxacillin-susceptible 42 ≤1-2 ≤1 ≤1 2
        Oxacillin-resistant 23 4->64 >64 32 >64
Staphylococcus epidermidis
    Cefepime
        Oxacillin-susceptible 39 ≤1 ≤1 ≤1 ≤1
        Oxacillin-resistant 17 ≤1-16 4 4 16
    Ceftriaxone
        Oxacillin-susceptible 39 ≤1-2 ≤1 ≤1 2
        Oxacillin-resistant 17 2-32 4 4 32
    Doripenem
        Oxacillin-susceptible 39 ≤0.015-0.06 0.03 0.03 0.03
        Oxacillin-resistant 17 ≤0.015-4 0.5 1 4
    Ertapenem
        Oxacillin-susceptible 39 0.12-0.5 0.25 0.25 0.25
        Oxacillin-resistant 17 0.25-32 2 2 16
    Imipenem
        Oxacillin-susceptible 39 ≤0.015 ≤0.015 ≤0.015 ≤0.015
        Oxacillin-resistant 17 0.03-4 0.06 0.12 2
    Meropenem
        Oxacillin-susceptible 39 0.03-0.12 0.06 0.06 0.06
        Oxacillin-resistant 17 0.06-16 1 1 8
    Piperacillin-tazobactam
        Oxacillin-susceptible 39 ≤1 ≤1 ≤1 ≤1
        Oxacillin-resistant 17 ≤1-4 ≤1 ≤1 4
Coagulase-negative staphylococci (non-S. epidermidis)
    Cefepime
        Oxacillin-susceptible 38 ≤1-4 ≤1 ≤1 2
        Oxacillin-resistant 24 ≤1->32 2 4 >32
    Ceftriaxone
        Oxacillin-susceptible 38 ≤1-16 ≤1 2 4
        Oxacillin-resistant 24 2->64 2 8 >64
    Doripenem
        Oxacillin-susceptible 38 ≤0.015-0.5 0.03 0.03 0.12
        Oxacillin-resistant 24 0.03-32 0.06 0.5 16
    Ertapenem
        Oxacillin-susceptible 38 0.06-2 0.25 0.25 0.5
        Oxacillin-resistant 24 0.12->32 >32 2 >32
    Imipenem
        Oxacillin-susceptible 38 ≤0.015-0.06 ≤0.015 ≤0.015 0.03
        Oxacillin-resistant 24 ≤0.015-32 0.03 0.06 8
    Meropenem
        Oxacillin-susceptible 38 ≤0.015-1 0.06 0.06 0.25
        Oxacillin-resistant 24 0.06->32 0.5 1 32
    Piperacillin-tazobactam
        Oxacillin-susceptible 38 ≤1-2 ≤1 ≤1 ≤1
        Oxacillin-resistant 24 ≤1->64 ≤1 2 64
Streptococcus pyogenes
    Penicillin
        Macrolide-susceptible 10 ≤0.06 ≤0.06 ≤0.06 ≤0.06
    Cefepime
        Macrolide-susceptible 10 ≤0.06 ≤0.06 ≤0.06 ≤0.06
    Ceftriaxone
        Macrolide-susceptible 10 ≤0.03 ≤0.03 ≤0.03 ≤0.03
    Doripenem
        Macrolide-susceptible 10 ≤0.008 ≤0.008 ≤0.008 ≤0.008
    Ertapenem
        Macrolide-susceptible 10 ≤0.008-0.015 ≤0.008 ≤0.008 ≤0.008
    Imipenem
        Macrolide-susceptible 10 ≤0.008 ≤0.008 ≤0.008 ≤0.008
    Meropenem
        Macrolide-susceptible 10 ≤0.008 ≤0.008 ≤0.008 ≤0.008
    Piperacillin-tazobactam
        Macrolide-susceptible 10 ≤0.06 ≤0.06 ≤0.06 ≤0.06
Streptococcus agalactiae
    Penicillin
        Macrolide-susceptible 20 ≤0.06 ≤0.06 ≤0.06 ≤0.06
        Macrolide-resistant 20 ≤0.06 ≤0.06 ≤0.06 ≤0.06
    Cefepime
        Macrolide-susceptible 20 ≤0.06-0.12 ≤0.06 ≤0.06 ≤0.06
        Macrolide-resistant 20 ≤0.06-0.12 ≤0.06 ≤0.06 0.12
    Ceftriaxone
        Macrolide-susceptible 20 ≤0.03-0.06 0.06 0.06 0.06
        Macrolide-resistant 20 ≤0.03-0.12 0.06 0.06 0.06
    Doripenem
        Macrolide-susceptible 20 ≤0.008-0.015 0.015 0.015 0.015
        Macrolide-resistant 20 0.015-0.03 0.015 0.015 0.015
    Ertapenem
        Macrolide-susceptible 20 0.03-0.06 0.03 0.03 0.06
        Macrolide-resistant 20 0.03-0.06 0.06 0.06 0.06
    Imipenem
        Macrolide-susceptible 20 ≤0.008-0.015 0.015 0.015 0.015
        Macrolide-resistant 20 ≤0.008-0.03 0.015 0.015 0.015
    Meropenem
        Macrolide-susceptible 20 0.03 0.03 0.03 0.03
        Macrolide-resistant 20 0.03-0.06 0.03 0.03 0.06
    Piperacillin-tazobactam
        Macrolide-susceptible 20 0.25-0.5 0.25 0.25 0.25
        Macrolide-resistant 20 0.25-0.5 0.25 0.25 0.5
Streptococcus pneumoniae
    Cefepime
        Penicillin-susceptible 44 ≤0.06 ≤0.06 ≤0.06 ≤0.06
        Penicillin-intermediate 23 ≤0.06-1 0.5 0.25 1
        Penicillin-resistant 33 0.5-4 1 1 2
    Ceftriaxone
        Penicillin-susceptible 44 ≤0.03 ≤0.03 ≤0.03 ≤0.03
        Penicillin-intermediate 23 ≤0.03-0.5 0.5 0.25 0.5
        Penicillin-resistant 33 0.5-8 1 1 4
    Doripenem
        Penicillin-susceptible 44 ≤0.008-0.015 ≤0.008 ≤0.008 ≤0.008
        Penicillin-intermediate 23 0.015-0.5 0.25 0.12 0.25
        Penicillin-resistant 33 0.25-1 1 0.5 1
    Ertapenem
        Penicillin-susceptible 44 ≤0.008-0.03 0.015 0.015 0.015
        Penicillin-intermediate 23 0.03-1 0.03 0.25 1
        Penicillin-resistant 33 0.5-4 0.5 1 2
    Imipenem
        Penicillin-susceptible 44 ≤0.008-0.015 ≤0.008 ≤0.008 ≤0.008
        Penicillin-intermediate 23 ≤0.008-0.25 0.12 0.06 0.12
        Penicillin-resistant 33 0.12-1 0.5 0.5 1
    Meropenem
        Penicillin-susceptible 44 ≤0.008-0.03 ≤0.008 ≤0.008 ≤0.008
        Penicillin-intermediate 23 0.015-0.5 0.25 0.12 0.5
        Penicillin-resistant 33 0.25-2 0.5 0.5 1
    Piperacillin-tazobactam
        Penicillin-susceptible 44 ≤0.06-0.12 ≤0.06 ≤0.06 ≤0.06
        Penicillin-intermediate 23 ≤0.06-4 2 1 4
        Penicillin-resistant 33 2->8 4 4 8
Viridans group streptococci
    Cefepime
        Penicillin-susceptible 38 ≤0.06-0.5 ≤0.06 0.12 0.5
        Penicillin-intermediate 4 0.25-1
        Penicillin-resistant 18 0.5->4 2 2 >4
    Ceftriaxone
        Penicillin-susceptible 38 ≤0.03-0.5 0.06 0.06 0.25
        Penicillin-intermediate 4 0.25-1
        Penicillin-resistant 18 1->8 4 4 4
    Doripenem
        Penicillin-susceptible 38 ≤0.008-0.06 0.03 0.03 0.06
        Penicillin-intermediate 4 0.03-1
        Penicillin-resistant 18 0.25-4 1 1 4
    Ertapenem
        Penicillin-susceptible 38 0.03-0.5 0.06 0.06 0.25
        Penicillin-intermediate 4 0.12-2
        Penicillin-resistant 18 1->8 4 4 8
    Imipenem
        Penicillin-susceptible 38 ≤0.008-0.06 0.015 0.015 0.06
        Penicillin-intermediate 4 0.03-1
        Penicillin-resistant 18 0.12-4 2 2 2
    Meropenem
        Penicillin-susceptible 38 ≤0.008-0.12 0.03 0.03 0.06
        Penicillin-intermediate 4 0.06-1
        Penicillin-resistant 18 0.25-4 2 2 4
    Piperacillin-tazobactam
        Penicillin-susceptible 38 ≤0.06-2 0.12 0.12 1
        Penicillin-intermediate 4 0.25-8
        Penicillin-resistant 18 0.5->8 >8 8 >8
a

MIC50, the MIC at which 50% of the isolates are inhibited by an antimicrobial agent. The mode, MIC50, and MIC90 were not calculated for phenotype groups of <10 isolates.

FIG. 1.

FIG. 1.

MIC distributions of doripenem, ertapenem, imipenem, and meropenem against 211 isolates of ESBL-negative or ceftazidime-susceptible Enterobacteriaceae (A) and 140 isolates of ESBL-positive or ceftazidime-intermediate or ceftazidime-resistant Enterobacteriaceae (B).

As demonstrated for ertapenem, imipenem, and meropenem, doripenem showed limited activity against enterococci (Table 1). Doripenem was more active against both vancomycin-resistant and vancomycin-susceptible isolates of Enterococcus faecalis (MIC90, 8 μg/ml) than against Enterococcus faecium (MIC90, >32 μg/ml).

Doripenem was more active against oxacillin-susceptible isolates (MIC90s, 0.03 to 0.12 μg/ml) than against oxacillin-resistant isolates (MIC90s, 4 to 32 μg/ml) of Staphylococcus aureus, Staphylococcus epidermidis, and coagulase-negative staphylococci other than S. epidermidis (Table 1). The MICs of doripenem for staphylococci were similar to those of imipenem and lower than those of ertapenem and meropenem. The MICs of all of the carbapenems including doripenem (Fig. 2) and the other β-lactams tested were higher for oxacillin-resistant staphylococci than for oxacillin-susceptible staphylococci.

FIG. 2.

FIG. 2.

MIC distributions of doripenem, ertapenem, imipenem, and meropenem against 42 isolates of oxacillin-susceptible S. aureus (A) and 23 isolates of oxacillin-resistant S. aureus (B).

Doripenem, ertapenem, imipenem, and meropenem MIC90s were all ≤0.008 μg/ml for Streptococcus pyogenes (Table 1). For Streptococcus agalactiae, the MIC90s of doripenem (0.015 μg/ml) and imipenem (0.015 μg/ml) were lower than those of ertapenem (0.06 μg/ml) and meropenem (0.03 to 0.06 μg/ml). For penicillin-susceptible Streptococcus pneumoniae, the MIC90s of doripenem, meropenem, imipenem, and ertapenem were ≤0.015 μg/ml; for penicillin-resistant S. pneumoniae, the MIC90s of all four carbapenems were 1 to 2 μg/ml (Table 1). The MIC distributions of doripenem, ertapenem, and imipenem were similar for penicillin-susceptible, penicillin-intermediate, and penicillin-resistant S. pneumoniae (Fig. 3); however, the MICs of ertapenem and meropenem were higher for all three subgroups of S. pneumoniae. For penicillin-susceptible and penicillin-resistant isolates belonging to the viridans group streptococci, the MIC90s of doripenem (penicillin-susceptible, 0.06 μg/ml; penicillin-resistant, 4 μg/ml), imipenem (0.06 μg/ml; 2 μg/ml), and meropenem (0.06 μg/ml; 4 μg/ml) were lower than those of ertapenem (0.25 μg/ml; 8 μg/ml). Expanded-spectrum cephalosporins and piperacillin-tazobactam were not as potent as doripenem, imipenem, and meropenem against both penicillin-susceptible and penicillin-resistant isolates.

FIG. 3.

FIG. 3.

MIC distributions of doripenem, ertapenem, imipenem, and meropenem against 44 isolates of penicillin-susceptible S. pneumoniae (A), 23 isolates of penicillin-intermediate S. pneumoniae (B), and 33 isolates of penicillin-resistant S. pneumoniae (C).

Overall, doripenem demonstrated in vitro activity similar to that of meropenem against gram-negative isolates and similar to that of imipenem against gram-positive isolates, confirming results reported by other investigators (6, 9, 11) (Table 1). Isolates of Enterobacteriaceae harboring ESBLs and/or inducible or derepressed AmpC β-lactamases are not associated with increased MICs of doripenem, imipenem, and meropenem relative to β-lactamase-free control isolates (S. Mushtaq, Y. Ge, and D. M. Livermore, Abstr. 43rd Intersci. Conf. Antimicrob. Agents Chemother., abstr. F-529, 2003; H. Huynh, P. R. Rhomberg, and R. N. Jones, Abstr. 43rd Intersci. Conf. Antimicrob. Agents Chemother., abstr. F-528, 2003) (Table 1). Doripenem, like all known carbapenems, is inactive against isolates of Enterobacteriaceae containing carbapenemases (S. Mushtaq et al., 43rd ICAAC; H. Huynh et al., 43rd ICAAC). Other preliminary studies have reported that doripenem has potent in vitro activity against Haemophilus influenzae, Moraxella catarrhalis, Aeromonas spp., Bacillus spp., Bordetella pertussis, and common gram-positive and gram-negative anaerobic bacteria and less or no activity in vitro against Cornynebacterium spp. and Stenotrophomonas maltophilia (6, 9, 11; R. N. Jones et al., 43rd ICAAC). Doripenem has also been reported to demonstrate activity against P. aeruginosa that is as potent as, or slightly more potent than, that of meropenem and imipenem (6, 9, 11; R. N. Jones et al., 43rd ICAAC).

Very limited animal study and clinical trial data have been published on doripenem (9; A. Saito, T. Inamatsu, and J. Shimada, Abstr. 37th Intersci. Conf. Antimicrob. Agents Chemother., abstr. F-219, 1997; D. A. Thye et al., 43rd ICAAC). In humans, approximately 60 to 75% of doripenem administered intravenously was recovered in the urine within 24 h (11; K. Shiba et al., 37th ICAAC; D. A. Thye et al., 43rd ICAAC) and maximum concentrations in serum of approximately 50 μg/ml were achieved following a 1,000-mg dose of doripenem given as an infusion over 1 h (D. A. Thye et al., 43rd ICAAC). Doripenem has not demonstrated the adverse effects associated with other carbapenems (renal toxicity and neurotoxicity) in two animal models (9) and in humans (D. A. Thye et al., 43rd ICAAC). Doripenem has also been reported to have a weaker neurological side-effect profile than imipenem and meropenem in an animal model (S. Hori, J. Sato, M. Kawamura, and J. Shimada, Abstr. 37th Intersci. Conf. Antimicrob. Agents Chemother., abstr. F-220, 1997).

Based upon the data generated in the present study, as well as on published data in other preliminary studies (6, 9, 11), further investigation of doripenem as a broad-spectrum parenteral agent is warranted.

Acknowledgments

This study was funded by Peninsula Pharmaceuticals, Inc., Alameda, Calif.

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