Dual-Targeting Approach Degrades Biofilm Matrix and Enhances Bacterial Killing

Author:

Ren Z.12,Kim D.2,Paula A.J.13ORCID,Hwang G.2,Liu Y.2,Li J.1,Daniell H.4,Koo H.2

Affiliation:

1. State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Cariology and Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, P.R. China

2. Biofilm Research Laboratories, Levy Center for Oral Health, Department of Orthodontics and Divisions of Pediatric Dentistry & Community Oral Health, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA

3. Solid-Biological Interface Group (SolBIN), Departamento de Física, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil

4. Department of Biochemistry, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA

Abstract

Biofilm formation is a key virulence factor responsible for a wide range of infectious diseases, including dental caries. Cariogenic biofilms are structured microbial communities embedded in an extracellular matrix that affords bacterial adhesion-cohesion and drug tolerance, making them difficult to treat using conventional antimicrobial monotherapy. Here, we investigated a multitargeted approach combining exopolysaccharide (EPS) matrix-degrading glucanohydrolases with a clinically used essential oils–based antimicrobial to potentiate antibiofilm efficacy. Our data showed that dextranase and mutanase can synergistically break down the EPS glucan matrix in preformed cariogenic biofilms, markedly enhancing bacterial killing by the antimicrobial agent (3-log increase versus antimicrobial alone). Further analyses revealed that an EPS-degrading/antimicrobial (EDA) approach disassembles the matrix scaffold, exposing the bacterial cells for efficient killing while concurrently causing cellular dispersion and “physical collapse” of the bacterial clusters. Unexpectedly, we found that the EDA approach can also selectively target the EPS-producing cariogenic bacteria Streptococcus mutans with higher killing specificity (versus other species) within mixed biofilms, disrupting their accumulation and promoting dominance of commensal bacteria. Together, these results demonstrate a dual-targeting approach that can enhance antibiofilm efficacy and precision by dismantling the EPS matrix and its protective microenvironment, amplifying the killing of pathogenic bacteria within.

Funder

National Natural Science Foundation of China

China Scholarship Council

National Key Technologies R&D Program of China during the 12th Five-Year Plan Period

Johnson&Johnson

Publisher

SAGE Publications

Subject

General Dentistry

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