Cargando…

N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1

Nosocomial infections pose serious health concerns with over 2 million reported annually in the United States. Many of these infections are associated with bacterial resistance to antibiotics and hence, alternative treatments are critically needed. The objective of this study was to assess the antim...

Descripción completa

Detalles Bibliográficos
Autores principales: Young, Mikaeel, Ozcan, Ali, Lee, Briana, Maxwell, Tyler, Andl, Thomas, Rajasekaran, Parthiban, Beazley, Melanie J., Tetard, Laurene, Santra, Swadeshmukul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789799/
https://www.ncbi.nlm.nih.gov/pubmed/31374947
http://dx.doi.org/10.3390/pathogens8030120
_version_ 1783458696727101440
author Young, Mikaeel
Ozcan, Ali
Lee, Briana
Maxwell, Tyler
Andl, Thomas
Rajasekaran, Parthiban
Beazley, Melanie J.
Tetard, Laurene
Santra, Swadeshmukul
author_facet Young, Mikaeel
Ozcan, Ali
Lee, Briana
Maxwell, Tyler
Andl, Thomas
Rajasekaran, Parthiban
Beazley, Melanie J.
Tetard, Laurene
Santra, Swadeshmukul
author_sort Young, Mikaeel
collection PubMed
description Nosocomial infections pose serious health concerns with over 2 million reported annually in the United States. Many of these infections are associated with bacterial resistance to antibiotics and hence, alternative treatments are critically needed. The objective of this study was to assess the antimicrobial efficacy of a gallium (Ga)-based particle coated with N-Acetyl Cysteine (Ga-NAC) against Pseudomonas aeruginosa PAO1. Our studies showed the Minimum Inhibitory Concentration (MIC) of PAO1 treated with Ga-NAC was 1 µg/mL. Cytotoxicity of Ga-NAC against multiple cell lines was determined with no cytotoxicity observed up to concentrations of 2000 µg/mL (metal concentration), indicating a high therapeutic window. To elucidate potential antibacterial modes of action, Inductively Coupled Plasma—Mass Spectrometry (ICP-MS), infrared spectroscopy, and atomic force microscopy (AFM) were used. The results suggest improved Ga(3+) interaction with PAO1 through Ga-NAC particles. No significant change in cell membrane chemistry or roughening was detected. As cell membrane integrity remained intact, the antimicrobial mode of action was linked to cellular internalization of Ga and subsequent iron metabolic disruption. Furthermore, Ga-NAC inhibited and disrupted biofilms seen with crystal violet assay and microscopy. Our findings suggest the Ga-NAC particle can potentially be used as an alternative to antibiotics for treatment of Pseudomonas aeruginosa infections.
format Online
Article
Text
id pubmed-6789799
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-67897992019-10-16 N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1 Young, Mikaeel Ozcan, Ali Lee, Briana Maxwell, Tyler Andl, Thomas Rajasekaran, Parthiban Beazley, Melanie J. Tetard, Laurene Santra, Swadeshmukul Pathogens Article Nosocomial infections pose serious health concerns with over 2 million reported annually in the United States. Many of these infections are associated with bacterial resistance to antibiotics and hence, alternative treatments are critically needed. The objective of this study was to assess the antimicrobial efficacy of a gallium (Ga)-based particle coated with N-Acetyl Cysteine (Ga-NAC) against Pseudomonas aeruginosa PAO1. Our studies showed the Minimum Inhibitory Concentration (MIC) of PAO1 treated with Ga-NAC was 1 µg/mL. Cytotoxicity of Ga-NAC against multiple cell lines was determined with no cytotoxicity observed up to concentrations of 2000 µg/mL (metal concentration), indicating a high therapeutic window. To elucidate potential antibacterial modes of action, Inductively Coupled Plasma—Mass Spectrometry (ICP-MS), infrared spectroscopy, and atomic force microscopy (AFM) were used. The results suggest improved Ga(3+) interaction with PAO1 through Ga-NAC particles. No significant change in cell membrane chemistry or roughening was detected. As cell membrane integrity remained intact, the antimicrobial mode of action was linked to cellular internalization of Ga and subsequent iron metabolic disruption. Furthermore, Ga-NAC inhibited and disrupted biofilms seen with crystal violet assay and microscopy. Our findings suggest the Ga-NAC particle can potentially be used as an alternative to antibiotics for treatment of Pseudomonas aeruginosa infections. MDPI 2019-08-01 /pmc/articles/PMC6789799/ /pubmed/31374947 http://dx.doi.org/10.3390/pathogens8030120 Text en © 2019 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
Young, Mikaeel
Ozcan, Ali
Lee, Briana
Maxwell, Tyler
Andl, Thomas
Rajasekaran, Parthiban
Beazley, Melanie J.
Tetard, Laurene
Santra, Swadeshmukul
N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1
title N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1
title_full N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1
title_fullStr N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1
title_full_unstemmed N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1
title_short N-acetyl Cysteine Coated Gallium Particles Demonstrate High Potency against Pseudomonas aeruginosa PAO1
title_sort n-acetyl cysteine coated gallium particles demonstrate high potency against pseudomonas aeruginosa pao1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789799/
https://www.ncbi.nlm.nih.gov/pubmed/31374947
http://dx.doi.org/10.3390/pathogens8030120
work_keys_str_mv AT youngmikaeel nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT ozcanali nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT leebriana nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT maxwelltyler nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT andlthomas nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT rajasekaranparthiban nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT beazleymelaniej nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT tetardlaurene nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1
AT santraswadeshmukul nacetylcysteinecoatedgalliumparticlesdemonstratehighpotencyagainstpseudomonasaeruginosapao1