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Antimicrobial Synergy Testing by the Inkjet Printer-assisted Automated Checkerboard Array and the Manual Time-kill Method
Published on: April 18, 2019
In Vitro Synergism of Penicillin and Ceftriaxone against Enterococcus faecalis
Lara Thieme1,2, Simon Briggs3, Eamon Duffy3
1Institute for Infectious Diseases and Infection Control, Jena University Hospital, Friedrich Schiller University, 07747 Jena, Germany.
Abstract:
Enterococcus faecalis infective endocarditis is commonly treated with intravenous ampicillin/ceftriaxone combination therapy. Ampicillin, however, is unsuitable for outpatient parenteral antibiotic therapy (OPAT) regimens due to its instability in 24 h continuous infusors, and has been successfully replaced by benzylpenicillin used together with ceftriaxone in a few small case series. Since in vitro synergy data of penicillin/ceftriaxone against E. faecalis are still lacking, checkerboard assays were performed for 28 clinical E. faecalis isolates and one laboratory standard strain. Synergistic effects (both lowest and median FICI) were observed for penicillin/ceftriaxone in 15/29 isolates, while ampicillin/ceftriaxone exhibited synergism in 22/29 isolates. For isolates with ceftriaxone MICs ≤ 256 mg/L, the addition of free ceftriaxone trough concentrations to penicillin or ampicillin resulted in comparable synergistic effects for both combinations. In contrast, for isolates with ceftriaxone MICs ≥ 512 mg/L free ceftriaxone trough concentrations were only sufficient to exhibit synergistic effects in combination with ampicillin, but not penicillin. This study suggests that benzylpenicillin/ceftriaxone would be expected to be suitable for the OPAT treatment of enterococcal endocarditis for E. faecalis isolates with ceftriaxone MICs ≤ 256 mg/L. However, combination therapy would be expected to provide no advantage over benzylpenicillin monotherapy for isolates with ceftriaxone MICs ≥ 512 mg/L. Further investigation is required to analyse the relationship between ceftriaxone susceptibility and penicillin/ceftriaxone synergy, especially for isolates with ceftriaxone MICs of 64 to 512 mg/L.
Insights
Benzylpenicillin/ceftriaxone shows promise for outpatient treatment of Enterococcus faecalis endocarditis, particularly for isolates with lower ceftriaxone resistance. Ampicillin/ceftriaxone remains more effective for highly resistant strains.
Area of Science:
- Infectious Diseases
- Pharmacology
- Microbiology
Background:
- Enterococcus faecalis infective endocarditis (IE) is typically treated with intravenous ampicillin/ceftriaxone.
- Ampicillin's instability in continuous infusion limits its use in outpatient parenteral antibiotic therapy (OPAT).
- Benzylpenicillin has been proposed as an alternative to ampicillin in OPAT for IE.
Purpose of the Study:
- To evaluate the in vitro synergy of benzylpenicillin/ceftriaxone against clinical isolates of Enterococcus faecalis.
- To compare the synergistic effects of benzylpenicillin/ceftriaxone with ampicillin/ceftriaxone.
- To determine the influence of ceftriaxone minimum inhibitory concentrations (MICs) on the synergy of these combinations.
Main Methods:
- Checkerboard assays were performed on 28 clinical Enterococcus faecalis isolates and one laboratory strain.
- Fractional Inhibitory Concentration Index (FICI) was used to assess synergistic effects.
- Isolates were categorized based on ceftriaxone MICs (≤ 256 mg/L and ≥ 512 mg/L).
Main Results:
- Benzylpenicillin/ceftriaxone demonstrated synergy in 15/29 isolates, while ampicillin/ceftriaxone showed synergy in 22/29 isolates.
- For isolates with ceftriaxone MICs ≤ 256 mg/L, both combinations yielded comparable synergistic effects.
- For isolates with ceftriaxone MICs ≥ 512 mg/L, only ampicillin/ceftriaxone exhibited synergistic effects.
Conclusions:
- Benzylpenicillin/ceftriaxone may be suitable for OPAT of E. faecalis IE with ceftriaxone MICs ≤ 256 mg/L.
- For isolates with ceftriaxone MICs ≥ 512 mg/L, benzylpenicillin/ceftriaxone offers no advantage over benzylpenicillin monotherapy.
- Further research is needed to clarify the relationship between ceftriaxone susceptibility and penicillin/ceftriaxone synergy.
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