Bacteriophage therapy reduces Staphylococcus aureus in a porcine and human ex vivo burn wound infection model

Author:

Molendijk Michèle M.12ORCID,Boekema Bouke K. H. L.3,Lattwein Kirby R.4,Vlig Marcel3,Bode Lonneke G. M.1,Koopmans Marion P. G.2,Verbon Annelies15,de Graaf Miranda2ORCID,van Wamel Willem J. B.1ORCID

Affiliation:

1. Department Medical Microbiology and Infectious Diseases, Erasmus MC, Rotterdam, the Netherlands

2. Department of Viroscience, Erasmus MC, Rotterdam, the Netherlands

3. Association of Dutch Burn Centres, Beverwijk, the Netherlands

4. Department of Cardiology, Erasmus MC, Rotterdam, the Netherlands

5. Department of Internal Medicine, UMC Utrecht, Utrecht, the Netherlands

Abstract

ABSTRACT Burn wounds are a major burden, with high mortality rates due to infections. Staphylococcus aureus is a major causative agent of burn wound infections, which can be difficult to treat because of antibiotic resistance and biofilm formation. An alternative to antibiotics is the use of bacteriophages, viruses that infect and kill bacteria. We investigated the efficacy of bacteriophage therapy for burn wound infections, in both a porcine and a newly developed human ex vivo skin model. In both models, the efficacy of a reference antibiotic treatment (fusidic acid) and bacteriophage treatment was determined for a single treatment, successive treatment, and prophylaxis. Both models showed a reduction in bacterial load after a single bacteriophage treatment. Increasing the frequency of bacteriophage treatments increased bacteriophage efficacy in the human ex vivo skin model, but not in the porcine model. In both models, prophylaxis with bacteriophages increased treatment efficacy. In all cases, bacteriophage treatment outperformed fusidic acid treatment. Both models allowed investigation of bacteriophage-bacteria dynamics in burn wounds. Overall, bacteriophage treatment outperformed antibiotic control underlining the potential of bacteriophage therapy for the treatment of burn wound infections, especially when used prophylactically.

Publisher

American Society for Microbiology

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