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Combination therapy: a way to limit emergence of resistance?
Abstract:
The ability of antibiotic combinations to limit the emergence of resistance during therapy was evaluated in a murine model. Peritonitis was produced by injecting a mixture containing 10(8) colony-forming units of bacteria and sterilized talcum into the peritoneum. Two hours later, a single antibiotic dose was administered subcutaneously. The next day, peritoneal bacterial populations were analyzed on Szybalski's gradients. Acquired resistance was recorded when there was at least a fourfold increase in minimum inhibitory concentrations compared with untreated animals. No resistance emerged after amikacin monotherapy (15 mg/kg); however, resistance was frequently observed after monotherapy with ceftriaxone (50 mg/kg) or pefloxacin (25 mg/kg). Resistance to ceftriaxone and pefloxacin emerged, respectively, in 15 percent and 83 percent of animals with Klebsiella pneumoniae, 71 percent and 54 percent with Enterobacter cloacae, 0 percent and 83 percent with Serratia marcescens, 25 percent and 100 percent with Pseudomonas aeruginosa, and 0 percent with both Escherichia coli and Staphylococcus aureus. In mice with K. pneumoniae or E. cloacae infections, any dual combination of amikacin, pefloxacin, and ceftriaxone produced less acquired resistance than did monotherapy. In these animals, the combination of ceftriaxone and pefloxacin abolished all resistance, whereas the combinations of amikacin plus ceftriaxone or amikacin plus pefloxacin reduced the frequency of resistance by more than half. In animals with P. aeruginosa or S. marcescens infections, resistance to pefloxacin diminished or disappeared after treatment with the combinations of pefloxacin plus ceftriaxone or pefloxacin plus amikacin. However, combinations with ceftriaxone resulted in more frequent resistance to ceftriaxone than did ceftriaxone alone. This was the case in P. aeruginosa infections treated with ceftriaxone plus amikacin (p less than 0.01), and in S. marcescens infections treated with ceftriaxone plus pefloxacin (p less than 0.05). Despite these certain notable exceptions, our data confirm that in most cases combination therapy does limit the emergence of resistance.
Insights
Antibiotic combinations effectively limit the emergence of antimicrobial resistance compared to monotherapy. This study in mice shows dual therapies significantly reduce resistance development in bacterial infections.
Area of Science:
- Microbiology
- Pharmacology
- Infectious Diseases
Background:
- Antimicrobial resistance is a growing global health threat.
- Monotherapy can lead to the rapid emergence of resistant bacterial strains.
- Combination antibiotic therapy is a potential strategy to mitigate resistance development.
Purpose of the Study:
- To evaluate the efficacy of antibiotic combinations in preventing acquired resistance during therapy.
- To compare resistance emergence rates between antibiotic monotherapy and combination therapy in a murine model of peritonitis.
Main Methods:
- A murine model of peritonitis was established using a mixture of bacteria and talcum.
- Animals received single-dose subcutaneous antibiotic treatments (amikacin, ceftriaxone, pefloxacin) or combinations.
- Bacterial populations and minimum inhibitory concentrations (MICs) were analyzed to determine acquired resistance.
Main Results:
- Amikacin monotherapy did not induce resistance, while ceftriaxone and pefloxacin monotherapies frequently did.
- Combination therapies, particularly ceftriaxone/pefloxacin, significantly reduced resistance emergence compared to monotherapy for Klebsiella pneumoniae and Enterobacter cloacae.
- Some combinations showed increased resistance to ceftriaxone in Pseudomonas aeruginosa and Serratia marcescens infections, despite reducing pefloxacin resistance.
Conclusions:
- Antibiotic combination therapy generally limits the emergence of acquired resistance.
- The effectiveness of combinations varies depending on the specific antibiotics and bacterial species involved.
- Careful selection of antibiotic combinations is crucial to maximize efficacy and minimize resistance development.