Abstract

Bacterial secondary metabolites are naturally produced to prevail amongst competitors in a shared habitat and thus represent a valuable source for antibiotic discovery. The transformation of newly discovered antibiotic compounds into effective drugs often requires additional surfactant components for drug formulation. Nature may also provide blueprints in this respect: A cocktail of two compounds consisting of the antibacterial red pigment prodigiosin and the biosurfactant serrawettin W1 is naturally produced by the bacterium Serratia marcescens, which occurs in highly competitive habitats including soil. We show here a combinatorial antibacterial effect of these compounds, but also of prodigiosin mixed with other (bio)surfactants, against the soil-dwelling bacterium Corynebacterium glutamicum taken as a model target bacterium. Prodigiosin exerted a combinatorial inhibitory effect with all tested surfactants in a disk diffusion assay which was especially pronounced in combination with N-myristoyltyrosine. Minimal inhibitory and bactericidal concentrations (MIC and MBC) of the individual compounds were 2.56 μg/mL prodigiosin and 32 μg/mL N-myristoyltyrosine, and the MIC of prodigiosin was decreased by 3 orders of magnitude to 0.005 μg/mL in the presence of 16 μg/mL N-myristoyltyrosine, indicative of synergistic interaction. Investigation of bacterial survival revealed similar combinatorial effects; moreover, antagonistic effects were observed at higher compound concentrations. Finally, the investigation of microcolony formation under combined application of concentrations just below the MBC revealed heterogeneity of responses with cell death or delayed growth. In summary, this study describes the combinatorial antibacterial effects of microbial biomolecules, which may have ecological relevance by inhibiting cohabiting species, but shall furthermore inspire drug development in the combat of infectious disease.

Highlights

  • Bacterial chemical defense mechanisms—developed to prevail amongst competitors in a shared habitat—have provided an ample source of effective antibiotics for clinical use [1], and continue to offer new promising drug candidates [2,3]

  • Additional surfactant components are required in the formulation of an effective drug; their major function in pharmaceuticals is to improve the solubility of drugs, and enable penetration across biological interfaces [4,5]

  • The antibacterial activities of compound mixtures were compared to the effects of single compounds on growth of the soil bacterium C. glutamicum, which constitutes a model system for Corynebacteriales [50,51], using a disk diffusion assay which represents an established method for initial straightforward determination of antibacterial effects [52]

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Summary

Introduction

Bacterial chemical defense mechanisms—developed to prevail amongst competitors in a shared habitat—have provided an ample source of effective antibiotics for clinical use [1], and continue to offer new promising drug candidates [2,3]. Additional surfactant components are required in the formulation of an effective drug; their major function in pharmaceuticals is to improve the solubility of drugs, and enable penetration across biological interfaces [4,5]. Since the application of synthetic surfactants for pharmaceutical formulations evoked discussions regarding potentially toxic byproducts or issues regarding lack of biodegradability [6,7], novel bio-based solutions appear attractive. Some bacteria living in highly competitive environments produce mixtures of antimicrobial and surface active compounds. It may be suspected that the surface active compound likewise enhances effectivity of the antibiotic by improving delivery to the target. Pigmented strains of the ubiquitous bacterium Serratia marcescens produce an antibiotic-surfactant mixture consisting of the red pigment prodigiosin and the antimicrobial biosurfactant serrawettin W1

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