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Anti-Biofilm Molecules Targeting Functional Amyloids
The choice of an effective therapeutic strategy in the treatment of biofilm-related infections is a significant issue. Amyloids, which have been historically related to human diseases, are now considered to be prevailing structural components of the biofilm matrix in a wide range of bacteria. This a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300730/ https://www.ncbi.nlm.nih.gov/pubmed/34210036 http://dx.doi.org/10.3390/antibiotics10070795 |
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author | Matilla-Cuenca, Leticia Toledo-Arana, Alejandro Valle, Jaione |
author_facet | Matilla-Cuenca, Leticia Toledo-Arana, Alejandro Valle, Jaione |
author_sort | Matilla-Cuenca, Leticia |
collection | PubMed |
description | The choice of an effective therapeutic strategy in the treatment of biofilm-related infections is a significant issue. Amyloids, which have been historically related to human diseases, are now considered to be prevailing structural components of the biofilm matrix in a wide range of bacteria. This assumption creates the potential for an exciting research area, in which functional amyloids are considered to be attractive targets for drug development to dissemble biofilm structures. The present review describes the best-characterized bacterial functional amyloids and focuses on anti-biofilm agents that target intrinsic and facultative amyloids. This study provides a better understanding of the different modes of actions of the anti-amyloid molecules to inhibit biofilm formation. This information can be further exploited to improve the therapeutic strategies to combat biofilm-related infections. |
format | Online Article Text |
id | pubmed-8300730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83007302021-07-24 Anti-Biofilm Molecules Targeting Functional Amyloids Matilla-Cuenca, Leticia Toledo-Arana, Alejandro Valle, Jaione Antibiotics (Basel) Review The choice of an effective therapeutic strategy in the treatment of biofilm-related infections is a significant issue. Amyloids, which have been historically related to human diseases, are now considered to be prevailing structural components of the biofilm matrix in a wide range of bacteria. This assumption creates the potential for an exciting research area, in which functional amyloids are considered to be attractive targets for drug development to dissemble biofilm structures. The present review describes the best-characterized bacterial functional amyloids and focuses on anti-biofilm agents that target intrinsic and facultative amyloids. This study provides a better understanding of the different modes of actions of the anti-amyloid molecules to inhibit biofilm formation. This information can be further exploited to improve the therapeutic strategies to combat biofilm-related infections. MDPI 2021-06-29 /pmc/articles/PMC8300730/ /pubmed/34210036 http://dx.doi.org/10.3390/antibiotics10070795 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Matilla-Cuenca, Leticia Toledo-Arana, Alejandro Valle, Jaione Anti-Biofilm Molecules Targeting Functional Amyloids |
title | Anti-Biofilm Molecules Targeting Functional Amyloids |
title_full | Anti-Biofilm Molecules Targeting Functional Amyloids |
title_fullStr | Anti-Biofilm Molecules Targeting Functional Amyloids |
title_full_unstemmed | Anti-Biofilm Molecules Targeting Functional Amyloids |
title_short | Anti-Biofilm Molecules Targeting Functional Amyloids |
title_sort | anti-biofilm molecules targeting functional amyloids |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300730/ https://www.ncbi.nlm.nih.gov/pubmed/34210036 http://dx.doi.org/10.3390/antibiotics10070795 |
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