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Updated: Jan 11, 2026

Quadruple-Checkerboard: A Modification of the Three-Dimensional Checkerboard for Studying Drug Combinations
Published on: July 24, 2021
Synergistic but clinically unattainable: amoxicillin/ceftriaxone combination against ampicillin-susceptible
Ahmed Ashrin1, Clémence Hagenimana1,2, Hervé Jacquier1,2
1Unité de Bactériologie, Département de Prévention, Diagnostic et Traitement des Infections, Hôpitaux Universitaires Henri Mondor-Albert Chenevier, Assistance Publique-Hôpitaux de Paris (AP-HP), Créteil 94010, France.
Background:
Infective endocarditis (IE) is a severe infection requiring efficient, sometimes combined, antibiotic therapy. For β-lactam-susceptible Enteroccus spp., particularly Enterococcus faecalis (EFS), the combination of amoxicillin and ceftriaxone is currently recommended. However, limited data are available for ampicillin-susceptible E. faecium strains (EFM-S).
Objectives:
To characterize the in vitro synergy of amoxicillin/ceftriaxone combination against clinical isolates of EFM-S and evaluate its clinical relevance.
Methods:
Twenty-six EFM-S and 10 EFS clinical isolates from the Henri Mondor Hospital (Créteil, France) were tested. EFM-S clades were previously determined by whole-genome sequencing. Checkerboard assays were performed to assess the MICs and synergy across a range of amoxicillin and ceftriaxone concentrations. The fractional inhibitory concentration (FIC) index was computed for each combination, with synergy defined as ΣFIC ≤ 0.5.
Results:
Amoxicillin and ceftriaxone MIC distributions were comparable between EFM-S (amoxicillin, 0.06-2 mg/L; ceftriaxone, 1 to ≥1024 mg/L) and EFS (amoxicillin, 0.5-2 mg/L; ceftriaxone, 64 to ≥1024 mg/L). Synergy was observed in 21/26 EFM-S and all EFS strains. The five non-synergistic EFM-S strains had low ceftriaxone MICs (1-16 mg/L), probably limiting synergy detection. No difference was observed according to EFM clades. The minimal synergistic concentrations were consistently higher for EFM-S (median amoxicillin, 0.125 mg/L; ceftriaxone, 32 mg/L) compared to EFS (amoxicillin, 0.03 mg/L; ceftriaxone, 2 mg/L).
Conclusions:
Despite in vitro synergy, the amoxicillin/ceftriaxone combination is clinically irrelevant for EFM-S IE due to unachievable drug concentrations in vivo. These findings support clearer guidelines explicitly excluding this regimen for E. faecium, regardless of β-lactam susceptibility.
Insights
The amoxicillin/ceftriaxone combination shows in vitro synergy against ampicillin-susceptible Enterococcus faecium (EFM-S) but is clinically irrelevant for infective endocarditis (IE). This suggests excluding this regimen for E. faecium infections due to unachievable drug concentrations.
Area of Science:
- Infectious Diseases
- Microbiology
- Pharmacology
Background:
- Infective endocarditis (IE) necessitates effective antibiotic strategies, often involving combination therapy.
- While amoxicillin/ceftriaxone is recommended for β-lactam-susceptible Enterococcus faecalis (EFS), data for ampicillin-susceptible Enterococcus faecium (EFM-S) are limited.
Purpose of the Study:
- To investigate the in vitro synergy of amoxicillin/ceftriaxone against clinical EFM-S isolates.
- To assess the clinical relevance of this antibiotic combination for EFM-S IE.
Main Methods:
- Checkerboard assays were used to determine minimum inhibitory concentrations (MICs) and synergy (ΣFIC ≤ 0.5) for amoxicillin/ceftriaxone against 26 EFM-S and 10 EFS isolates.
- Whole-genome sequencing was previously performed to determine EFM-S clades.
Main Results:
- Synergy was observed in 21/26 EFM-S strains and all EFS strains.
- Minimal synergistic concentrations were higher for EFM-S compared to EFS.
- Five non-synergistic EFM-S strains exhibited low ceftriaxone MICs, potentially limiting synergy detection.
Conclusions:
- Despite observed in vitro synergy, the amoxicillin/ceftriaxone combination is clinically irrelevant for EFM-S IE.
- Unachievable in vivo drug concentrations render this regimen ineffective for E. faecium infections.
- Clearer guidelines are needed to exclude this combination for E. faecium, irrespective of β-lactam susceptibility.
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