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Small-Molecule Inhibition of Bacterial Biofilm

[Image: see text] Antibiotic resistance is a massive and serious threat to human welfare and healthcare. Apart from being genetically resistant to antibiotics, the other important mechanism by which bacteria can evade antibiotics is multidrug tolerance. Here cells enter into a transiently nongrowing...

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Autores principales: Ghosh, Anirban, Jayaraman, Narayansaswamy, Chatterji, Dipankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045314/
https://www.ncbi.nlm.nih.gov/pubmed/32118127
http://dx.doi.org/10.1021/acsomega.9b03695
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author Ghosh, Anirban
Jayaraman, Narayansaswamy
Chatterji, Dipankar
author_facet Ghosh, Anirban
Jayaraman, Narayansaswamy
Chatterji, Dipankar
author_sort Ghosh, Anirban
collection PubMed
description [Image: see text] Antibiotic resistance is a massive and serious threat to human welfare and healthcare. Apart from being genetically resistant to antibiotics, the other important mechanism by which bacteria can evade antibiotics is multidrug tolerance. Here cells enter into a transiently nongrowing phase, and as a result, latent infection remains inside the host, causing disease recurrence. Biofilm-derived antibiotic tolerance and persister formation of the pathogenic bacteria inside the host remain a serious issue of treatment failure and recurrent chronic infection in the case of all major pathogens. As a result, new chemotherapeutic agents are sought that specifically inhibit biofilm formation or maturation as well as cause the dispersion of mature biofilms, thus allowing the conventional drugs to kill sensitive cells residing inside. This mini-review attempts to analyze different small-molecule-based chemical approaches that have been used to enable bacterial biofilm inhibition at different steps of maturation.
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spelling pubmed-70453142020-02-28 Small-Molecule Inhibition of Bacterial Biofilm Ghosh, Anirban Jayaraman, Narayansaswamy Chatterji, Dipankar ACS Omega [Image: see text] Antibiotic resistance is a massive and serious threat to human welfare and healthcare. Apart from being genetically resistant to antibiotics, the other important mechanism by which bacteria can evade antibiotics is multidrug tolerance. Here cells enter into a transiently nongrowing phase, and as a result, latent infection remains inside the host, causing disease recurrence. Biofilm-derived antibiotic tolerance and persister formation of the pathogenic bacteria inside the host remain a serious issue of treatment failure and recurrent chronic infection in the case of all major pathogens. As a result, new chemotherapeutic agents are sought that specifically inhibit biofilm formation or maturation as well as cause the dispersion of mature biofilms, thus allowing the conventional drugs to kill sensitive cells residing inside. This mini-review attempts to analyze different small-molecule-based chemical approaches that have been used to enable bacterial biofilm inhibition at different steps of maturation. American Chemical Society 2020-02-12 /pmc/articles/PMC7045314/ /pubmed/32118127 http://dx.doi.org/10.1021/acsomega.9b03695 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Ghosh, Anirban
Jayaraman, Narayansaswamy
Chatterji, Dipankar
Small-Molecule Inhibition of Bacterial Biofilm
title Small-Molecule Inhibition of Bacterial Biofilm
title_full Small-Molecule Inhibition of Bacterial Biofilm
title_fullStr Small-Molecule Inhibition of Bacterial Biofilm
title_full_unstemmed Small-Molecule Inhibition of Bacterial Biofilm
title_short Small-Molecule Inhibition of Bacterial Biofilm
title_sort small-molecule inhibition of bacterial biofilm
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045314/
https://www.ncbi.nlm.nih.gov/pubmed/32118127
http://dx.doi.org/10.1021/acsomega.9b03695
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