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D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation
OBJECTIVE: Pseudomonas aeruginosa, a known biofilm‐forming organism, is an opportunistic pathogen that plays an important role in chronic otitis media, tracheitis, cholesteatoma, chronic wounds, and implant infections. Eradication of biofilm infections has been a challenge because the biofilm phenot...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324625/ https://www.ncbi.nlm.nih.gov/pubmed/28286870 http://dx.doi.org/10.1002/lio2.34 |
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author | Kao, Wee Tin K Frye, Mitchell Gagnon, Patricia Vogel, Joseph P. Chole, Richard |
author_facet | Kao, Wee Tin K Frye, Mitchell Gagnon, Patricia Vogel, Joseph P. Chole, Richard |
author_sort | Kao, Wee Tin K |
collection | PubMed |
description | OBJECTIVE: Pseudomonas aeruginosa, a known biofilm‐forming organism, is an opportunistic pathogen that plays an important role in chronic otitis media, tracheitis, cholesteatoma, chronic wounds, and implant infections. Eradication of biofilm infections has been a challenge because the biofilm phenotype provides bacteria with a protective environment from the immune system and antibiotics; thus, there has been great interest in adjunctive molecules that may inhibit biofilm formation or cause biofilm dispersal. There are reports that D‐amino acids may inhibit biofilms. In this study, we test the ability of various D‐amino acids to inhibit P. aeruginosa biofilm formation in vitro. STUDY DESIGN: We evaluated the effect of D‐alanine (10 mM), D‐leucine (10 mM), D‐methionine (10 mM), D‐tryptophan (10 mM), and D‐tyrosine (10 uM and 1 mM) on biofilm formation in two commonly studied laboratory strains of P. aeruginosa: PAO1 and PA14. METHODS: Biofilms were grown in 24‐well and 96‐well tissue culture plates, documented photographically and stained with 0.1% crystal violet and solubilized in 33% glacial acetic acid for quantification. RESULTS: In strains PAO1 and PA14, the addition of D‐amino acids did not result in an inhibitory effect on biofilm growth in 24‐well plates. Repeating the study in 96‐well plates confirmed our findings that D‐amino acids do not inhibit biofilm formation of P. aeruginosa. CONCLUSION: We conclude that D‐amino acids only slow the production of biofilms rather than completely prevent biofilm formation; therefore, D‐amino acids represent a poor option for potential clinically therapeutic interventions. LEVEL OF EVIDENCE: N/A. |
format | Online Article Text |
id | pubmed-5324625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53246252017-03-08 D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation Kao, Wee Tin K Frye, Mitchell Gagnon, Patricia Vogel, Joseph P. Chole, Richard Laryngoscope Investig Otolaryngol General Otolaryngology OBJECTIVE: Pseudomonas aeruginosa, a known biofilm‐forming organism, is an opportunistic pathogen that plays an important role in chronic otitis media, tracheitis, cholesteatoma, chronic wounds, and implant infections. Eradication of biofilm infections has been a challenge because the biofilm phenotype provides bacteria with a protective environment from the immune system and antibiotics; thus, there has been great interest in adjunctive molecules that may inhibit biofilm formation or cause biofilm dispersal. There are reports that D‐amino acids may inhibit biofilms. In this study, we test the ability of various D‐amino acids to inhibit P. aeruginosa biofilm formation in vitro. STUDY DESIGN: We evaluated the effect of D‐alanine (10 mM), D‐leucine (10 mM), D‐methionine (10 mM), D‐tryptophan (10 mM), and D‐tyrosine (10 uM and 1 mM) on biofilm formation in two commonly studied laboratory strains of P. aeruginosa: PAO1 and PA14. METHODS: Biofilms were grown in 24‐well and 96‐well tissue culture plates, documented photographically and stained with 0.1% crystal violet and solubilized in 33% glacial acetic acid for quantification. RESULTS: In strains PAO1 and PA14, the addition of D‐amino acids did not result in an inhibitory effect on biofilm growth in 24‐well plates. Repeating the study in 96‐well plates confirmed our findings that D‐amino acids do not inhibit biofilm formation of P. aeruginosa. CONCLUSION: We conclude that D‐amino acids only slow the production of biofilms rather than completely prevent biofilm formation; therefore, D‐amino acids represent a poor option for potential clinically therapeutic interventions. LEVEL OF EVIDENCE: N/A. John Wiley and Sons Inc. 2016-12-23 /pmc/articles/PMC5324625/ /pubmed/28286870 http://dx.doi.org/10.1002/lio2.34 Text en © 2016 The Authors Laryngoscope Investigative Otolaryngology published by Wiley Periodicals, Inc. on behalf of The Triological Society This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | General Otolaryngology Kao, Wee Tin K Frye, Mitchell Gagnon, Patricia Vogel, Joseph P. Chole, Richard D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation |
title | D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation |
title_full | D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation |
title_fullStr | D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation |
title_full_unstemmed | D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation |
title_short | D‐amino acids do not inhibit Pseudomonas aeruginosa biofilm formation |
title_sort | d‐amino acids do not inhibit pseudomonas aeruginosa biofilm formation |
topic | General Otolaryngology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324625/ https://www.ncbi.nlm.nih.gov/pubmed/28286870 http://dx.doi.org/10.1002/lio2.34 |
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