Abstract

Bacterial biofilms represent a major concern at a worldwide level due to the high demand for implantable medical devices and the rising numbers of bacterial resistance. The complex structure of the extracellular polymeric substances (EPS) matrix plays a major role in this phenomenon, since it protects bacteria from antibiotics, avoiding drug penetration at bactericidal concentrations. Besides, this structure promotes bacterial cells to adopt a dormant lifestyle, becoming less susceptible to antibacterial agents. Currently, the available treatment for biofilm-related infections consists in the administration of conventional antibiotics at high doses for a long-term period. However, this treatment lacks efficiency against mature biofilms and for implant-associated biofilms it may be necessary to remove the medical device. Thus, biofilm-related infections represent an economical burden for the healthcare systems. New strategies focusing on the matrix are being highlighted as alternative therapies to eradicate biofilms. Here, we outline reported matrix disruptive agents, nanocarriers, and technologies, such as application of magnetic fields, photodynamic therapy, and ultrasounds, that have been under investigation to disrupt the EPS matrix of clinically relevant bacterial biofilms. In an ideal therapy, a synergistic effect between antibiotics and the explored innovated strategies is aimed to completely eradicate biofilms and avoid antimicrobial resistance phenomena.

Highlights

  • A post-antibiotic era is emerging due to the increasing figures of antimicrobial resistance cases at a worldwide level

  • Biofilms are formed when bacterial cells attach to a substratum or to other cells embedded in a protective polymeric extracellular matrix (Pinto et al, 2019)

  • This review provides an overview of the characteristics of the extracellular polymeric substances (EPS) matrix and its role in antibiotic resistance

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Summary

Introduction

A post-antibiotic era is emerging due to the increasing figures of antimicrobial resistance cases at a worldwide level. With the purpose to combine antibacterial and antibiofilm agents in a nanocarrier, Tan et al developed positively charged chitosan NPs co-encapsulating oxacillin and DNase I to eradicate 24 h-old S. aureus mature biofilms.

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