Cargando…

Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections

Biofilm describes a microbially-derived sessile community in which microbial cells are firmly attached to the substratum and embedded in extracellular polymeric matrix. Microbial biofilms account for up to 80% of all bacterial and fungal infections in humans. Biofilm-associated pathogens are particu...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Xiaoqing, Huang, Ying-Ying, Wang, Yuguang, Wang, Xiaoyuan, Hamblin, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030385/
https://www.ncbi.nlm.nih.gov/pubmed/29997579
http://dx.doi.org/10.3389/fmicb.2018.01299
_version_ 1783337141207564288
author Hu, Xiaoqing
Huang, Ying-Ying
Wang, Yuguang
Wang, Xiaoyuan
Hamblin, Michael R.
author_facet Hu, Xiaoqing
Huang, Ying-Ying
Wang, Yuguang
Wang, Xiaoyuan
Hamblin, Michael R.
author_sort Hu, Xiaoqing
collection PubMed
description Biofilm describes a microbially-derived sessile community in which microbial cells are firmly attached to the substratum and embedded in extracellular polymeric matrix. Microbial biofilms account for up to 80% of all bacterial and fungal infections in humans. Biofilm-associated pathogens are particularly resistant to antibiotic treatment, and thus novel antibiofilm approaches needed to be developed. Antimicrobial Photodynamic therapy (aPDT) had been recently proposed to combat clinically relevant biofilms such as dental biofilms, ventilator associated pneumonia, chronic wound infections, oral candidiasis, and chronic rhinosinusitis. aPDT uses non-toxic dyes called photosensitizers (PS), which can be excited by harmless visible light to produce reactive oxygen species (ROS). aPDT is a multi-stage process including topical PS administration, light irradiation, and interaction of the excited state with ambient oxygen. Numerous in vitro and in vivo aPDT studies have demonstrated biofilm-eradication or substantial reduction. ROS are produced upon photo-activation and attack adjacent targets, including proteins, lipids, and nucleic acids present within the biofilm matrix, on the cell surface and inside the microbial cells. Damage to non-specific targets leads to the destruction of both planktonic cells and biofilms. The review aims to summarize the progress of aPDT in destroying biofilms and the mechanisms mediated by ROS. Finally, a brief section provides suggestions for future research.
format Online
Article
Text
id pubmed-6030385
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-60303852018-07-11 Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections Hu, Xiaoqing Huang, Ying-Ying Wang, Yuguang Wang, Xiaoyuan Hamblin, Michael R. Front Microbiol Microbiology Biofilm describes a microbially-derived sessile community in which microbial cells are firmly attached to the substratum and embedded in extracellular polymeric matrix. Microbial biofilms account for up to 80% of all bacterial and fungal infections in humans. Biofilm-associated pathogens are particularly resistant to antibiotic treatment, and thus novel antibiofilm approaches needed to be developed. Antimicrobial Photodynamic therapy (aPDT) had been recently proposed to combat clinically relevant biofilms such as dental biofilms, ventilator associated pneumonia, chronic wound infections, oral candidiasis, and chronic rhinosinusitis. aPDT uses non-toxic dyes called photosensitizers (PS), which can be excited by harmless visible light to produce reactive oxygen species (ROS). aPDT is a multi-stage process including topical PS administration, light irradiation, and interaction of the excited state with ambient oxygen. Numerous in vitro and in vivo aPDT studies have demonstrated biofilm-eradication or substantial reduction. ROS are produced upon photo-activation and attack adjacent targets, including proteins, lipids, and nucleic acids present within the biofilm matrix, on the cell surface and inside the microbial cells. Damage to non-specific targets leads to the destruction of both planktonic cells and biofilms. The review aims to summarize the progress of aPDT in destroying biofilms and the mechanisms mediated by ROS. Finally, a brief section provides suggestions for future research. Frontiers Media S.A. 2018-06-27 /pmc/articles/PMC6030385/ /pubmed/29997579 http://dx.doi.org/10.3389/fmicb.2018.01299 Text en Copyright © 2018 Hu, Huang, Wang, Wang and Hamblin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Hu, Xiaoqing
Huang, Ying-Ying
Wang, Yuguang
Wang, Xiaoyuan
Hamblin, Michael R.
Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections
title Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections
title_full Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections
title_fullStr Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections
title_full_unstemmed Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections
title_short Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections
title_sort antimicrobial photodynamic therapy to control clinically relevant biofilm infections
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030385/
https://www.ncbi.nlm.nih.gov/pubmed/29997579
http://dx.doi.org/10.3389/fmicb.2018.01299
work_keys_str_mv AT huxiaoqing antimicrobialphotodynamictherapytocontrolclinicallyrelevantbiofilminfections
AT huangyingying antimicrobialphotodynamictherapytocontrolclinicallyrelevantbiofilminfections
AT wangyuguang antimicrobialphotodynamictherapytocontrolclinicallyrelevantbiofilminfections
AT wangxiaoyuan antimicrobialphotodynamictherapytocontrolclinicallyrelevantbiofilminfections
AT hamblinmichaelr antimicrobialphotodynamictherapytocontrolclinicallyrelevantbiofilminfections