In Vitro Activities of Ertapenem (MK-0826) against Recent Clinical Bacteria Collected in Europe and Australia

Author:

Livermore David M.1,Carter Michael W.1,Bagel Simone2,Wiedemann Bernd2,Baquero Fernando,Loza Elena3,Endtz Hubert P.4,van den Braak Nicole4,Fernandes Clarence J.5,Fernandes Lorna5,Frimodt-Moller Niels6,Rasmussen Laura S.6,Giamarellou Helen7,Giamarellos-Bourboulis Evangelos7,Jarlier Vincent8,Nguyen Jacqueline8,Nord Carl-Erik9,Struelens Marc J.10,Nonhoff Caire10,Turnidge John11,Bell Jan11,Zbinden Reinhard12,Pfister Stefan,Mixson Lori13,Shungu Daniel L.14

Affiliation:

1. Antibiotic Resistance Monitoring & Reference Laboratory, Central Public Health Laboratory, London, United Kingdom1;

2. Pharmazeutische Mikrobiologie, Bonn, Germany2;

3. Servicio de Microbiologia, Hospital Ramon y Cajal, Madrid, Spain3;

4. Afdeling Medische Microbiologir & Infectieziekten, Academisch Ziekenhuis Totterdam, Rotterdam, The Netherlands4;

5. Microbiology Department, Pacific Laboratory Medicine Services, Royal North Shore Hospital, St. Leonards, New South Wales5 and

6. Department of Clinical Microbiology, Statens Serum Institut, Copenhagen, Denmark6;

7. Department of Internal Medicine, Athens Medical School, Athens, Greece7;

8. Laboratoire de Bacteriologie, Faculte de Medecine, Pitie-Salpetriere, Paris, France8;

9. Department of Microbiology, Huddinge University Hospital, Huddinge, Sweden9;

10. Universite Libre de Bruxelles, Clinique Universitaire, Brussels, Belgium10;

11. Microbiology and Infectious Diseases, Women's and Children's Hospital, North Adelaide, South Australia,11 Australia;

12. Department of Medical Microbiology, University of Zurich, Zurich, Switzerland12; and

13. Biometrics Research,13 and

14. Infectious Diseases, Clinical Microbiology Services,14 Merck Research Laboratories, Rahway, New Jersey

Abstract

ABSTRACT Ertapenem (MK-0826, L-749,345) is a 1-β-methyl carbapenem with a long serum half-life. Its in vitro activity was determined by broth microdilution against 3,478 bacteria from 12 centers in Europe and Australia, with imipenem, cefepime, ceftriaxone, and piperacillin-tazobactam used as comparators. Ertapenem was the most active agent tested against members of the family Enterobacteriaceae , with MICs at which 90% of isolates are inhibited (MIC 90 s) of ≤1 μg/ml for all species. Ertapenem also was more active than imipenem against fastidious gram-negative bacteria and Moraxella spp.; on the other hand, ertapenem was slightly less active than imipenem against streptococci, methicillin-susceptible staphylococci, and anaerobes, but its MIC 90 s for these groups remained ≤0.5 μg/ml. Acinetobacter spp. and Pseudomonas aeruginosa were also much less susceptible to ertapenem than imipenem, and most Enterococcus faecalis strains were resistant. Ertapenem resistance, based on a provisional NCCLS MIC breakpoint of ≥16 μg/ml, was seen in only 3 of 1,611 strains of the family Enterobacteriaceae tested, all of them Enterobacter aerogenes . Resistance was also seen in 2 of 135 anaerobes, comprising 1 Bacteroides fragilis strain and 1 Clostridium difficile strain. Ertapenem breakpoints for streptococci have not been established, but an unofficial susceptibility breakpoint of ≤2 μg/ml was adopted for clinical trials to generate corresponding clinical response data for isolates for which MICs were as high as 2 μg/ml. Of 234 Streptococcus pneumoniae strains tested, 2 required ertapenem MICs of 2 μg/ml and one required an MIC of 4 μg/ml, among 67 non- Streptococcus pyogenes , non- Streptococcus pneumoniae streptococci, single isolates required ertapenem MICs of 2 and 16 μg/ml. These streptococci also had diminished susceptibilities to other β-lactams, including imipenem as well as ertapenem. The Etest and disk diffusion gave susceptibility test results in good agreement with those of the broth microdilution method for ertapenem.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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