Abstract

Biofilms are an emerging target for new therapeutics in the effort to address the continued increase in resistance and tolerance to traditional antimicrobials. In particular, the distinct nature of the biofilm growth state often means that traditional antimcirobials, developed to combat planktonic cells, are ineffective. Biofilm treatments are designed to both reduce pathogen load at an infection site and decrease the development of resistance by rendering the embedded organisms more susceptible to treatment at lower antimicrobial concentrations. In this work, we developed a new antimicrobial treatment modality using engineered lactic acid bacteria (LAB). We first characterized the natural capacity of two lactobacilli, L. plantarum and L. rhamnosus, to inhibit P. aeruginosa growth, biofilm formation, and biofilm viability, which we found to be dependent upon the low pH generated during culture of the LAB. We further engineered these LAB to secrete enzymes known to degrade P. aeruginosa biofilms and show that our best performing engineered LAB, secreting a pathogen-derived enzyme (PelAh), degrades up to 85% of P. aeruginosa biofilm.

Highlights

  • As an important virulence factor for pathogenic microbes, biofilms are associated with an expanding array of pathologies, including various airway, gastrointestinal, and ocular infections, endocarditis, periodontitis, osteomyelitis, cystitis, and chronic wounds[1,2,3,4,5,6,7]

  • Workflow for c and d is shown: The lactic acid bacteria (LAB) supernatants were inoculated with PA14, which were serially diluted into fresh PA14 cultures

  • LAB effect their antimicrobial activity though a variety of mechanisms, including the production of antimicrobial proteins/ peptides, inhibitory metabolites, and organic acids

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Summary

Introduction

As an important virulence factor for pathogenic microbes, biofilms are associated with an expanding array of pathologies, including various airway, gastrointestinal, and ocular infections, endocarditis, periodontitis, osteomyelitis, cystitis, and chronic wounds[1,2,3,4,5,6,7]. Isogenic cells exhibit phenotypic diversity that is driven by the discrete microenvironments created by metabolite, ion, gas, and antimicrobial gradients within the biofilm. This phenotypic diversity manifests as distinct tolerances or resistances to traditional antimicrobials as well as the host immune system[9,10]. Clearance of mature biofilms is an essential component for the successful resolution of numerous infections, especially those that are chronic or recurrent in nature

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