Cargando…

The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa

Targeting the iron requirement of Pseudomonas aeruginosa may be an effective adjunctive for conventional antibiotic treatment against biofilm-dwelling P. aeruginosa. We, therefore, assessed the anti-biofilm activity of N,N’-bis (2-hydroxybenzyl) ethylenediamine-N,N’-diacetic acid (HBED), which is a...

Descripción completa

Detalles Bibliográficos
Autores principales: Mettrick, Karla, Hassan, Karl, Lamont, Iain, Reid, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235823/
https://www.ncbi.nlm.nih.gov/pubmed/32230813
http://dx.doi.org/10.3390/antibiotics9040144
_version_ 1783536043996217344
author Mettrick, Karla
Hassan, Karl
Lamont, Iain
Reid, David
author_facet Mettrick, Karla
Hassan, Karl
Lamont, Iain
Reid, David
author_sort Mettrick, Karla
collection PubMed
description Targeting the iron requirement of Pseudomonas aeruginosa may be an effective adjunctive for conventional antibiotic treatment against biofilm-dwelling P. aeruginosa. We, therefore, assessed the anti-biofilm activity of N,N’-bis (2-hydroxybenzyl) ethylenediamine-N,N’-diacetic acid (HBED), which is a synthetic hexadentate iron chelator. The effect of HBED was studied using short-term (microtitre plate) and longer-term (flow-cell) biofilm models, under aerobic, anaerobic, and microaerobic (flow-cell) conditions and in combination with the polymyxin antibiotic colistimethate sodium (colistin). HBED was assessed against strains of P. aeruginosa from patients with cystic fibrosis and the reference strain PAO1. HBED inhibited growth and biofilm formation of all clinical strains under aerobic and anaerobic conditions, but inhibitory effects against PAO1 were predominantly exerted under anaerobic conditions. PA605, which is a clinical strain with a robust biofilm-forming phenotype, was selected for flow-cell studies. HBED significantly reduced biomass and surface coverage of PA605, and, combined with colistin, HBED significantly enhanced the microcolony killing effects of colistin to result in almost complete removal of the biofilm. HBED combined with colistin is highly effective in vitro against biofilms formed by clinical strains of P. aeruginosa.
format Online
Article
Text
id pubmed-7235823
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-72358232020-05-22 The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa Mettrick, Karla Hassan, Karl Lamont, Iain Reid, David Antibiotics (Basel) Article Targeting the iron requirement of Pseudomonas aeruginosa may be an effective adjunctive for conventional antibiotic treatment against biofilm-dwelling P. aeruginosa. We, therefore, assessed the anti-biofilm activity of N,N’-bis (2-hydroxybenzyl) ethylenediamine-N,N’-diacetic acid (HBED), which is a synthetic hexadentate iron chelator. The effect of HBED was studied using short-term (microtitre plate) and longer-term (flow-cell) biofilm models, under aerobic, anaerobic, and microaerobic (flow-cell) conditions and in combination with the polymyxin antibiotic colistimethate sodium (colistin). HBED was assessed against strains of P. aeruginosa from patients with cystic fibrosis and the reference strain PAO1. HBED inhibited growth and biofilm formation of all clinical strains under aerobic and anaerobic conditions, but inhibitory effects against PAO1 were predominantly exerted under anaerobic conditions. PA605, which is a clinical strain with a robust biofilm-forming phenotype, was selected for flow-cell studies. HBED significantly reduced biomass and surface coverage of PA605, and, combined with colistin, HBED significantly enhanced the microcolony killing effects of colistin to result in almost complete removal of the biofilm. HBED combined with colistin is highly effective in vitro against biofilms formed by clinical strains of P. aeruginosa. MDPI 2020-03-27 /pmc/articles/PMC7235823/ /pubmed/32230813 http://dx.doi.org/10.3390/antibiotics9040144 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mettrick, Karla
Hassan, Karl
Lamont, Iain
Reid, David
The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa
title The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa
title_full The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa
title_fullStr The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa
title_full_unstemmed The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa
title_short The Iron-chelator, N,N’-bis (2-hydroxybenzyl) Ethylenediamine-N,N’-diacetic acid is an Effective Colistin Adjunct against Clinical Strains of Biofilm-Dwelling Pseudomonas aeruginosa
title_sort iron-chelator, n,n’-bis (2-hydroxybenzyl) ethylenediamine-n,n’-diacetic acid is an effective colistin adjunct against clinical strains of biofilm-dwelling pseudomonas aeruginosa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235823/
https://www.ncbi.nlm.nih.gov/pubmed/32230813
http://dx.doi.org/10.3390/antibiotics9040144
work_keys_str_mv AT mettrickkarla theironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa
AT hassankarl theironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa
AT lamontiain theironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa
AT reiddavid theironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa
AT mettrickkarla ironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa
AT hassankarl ironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa
AT lamontiain ironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa
AT reiddavid ironchelatornnbis2hydroxybenzylethylenediaminenndiaceticacidisaneffectivecolistinadjunctagainstclinicalstrainsofbiofilmdwellingpseudomonasaeruginosa