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Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli

Vibrio cholerae and enterotoxic Escherichia coli (ETEC) remain two dominant bacterial causes of severe secretory diarrhea and still a significant cause of death, especially in developing countries. In order to investigate new effective and inexpensive therapeutic approaches, we analyzed nanoparticle...

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Autores principales: Salem, Wesam, Leitner, Deborah R., Zingl, Franz G., Schratter, Gebhart, Prassl, Ruth, Goessler, Walter, Reidl, Joachim, Schild, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Urban & Fischer Verlag 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300426/
https://www.ncbi.nlm.nih.gov/pubmed/25466205
http://dx.doi.org/10.1016/j.ijmm.2014.11.005
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author Salem, Wesam
Leitner, Deborah R.
Zingl, Franz G.
Schratter, Gebhart
Prassl, Ruth
Goessler, Walter
Reidl, Joachim
Schild, Stefan
author_facet Salem, Wesam
Leitner, Deborah R.
Zingl, Franz G.
Schratter, Gebhart
Prassl, Ruth
Goessler, Walter
Reidl, Joachim
Schild, Stefan
author_sort Salem, Wesam
collection PubMed
description Vibrio cholerae and enterotoxic Escherichia coli (ETEC) remain two dominant bacterial causes of severe secretory diarrhea and still a significant cause of death, especially in developing countries. In order to investigate new effective and inexpensive therapeutic approaches, we analyzed nanoparticles synthesized by a green approach using corresponding salt (silver or zinc nitrate) with aqueous extract of Caltropis procera fruit or leaves. We characterized the quantity and quality of nanoparticles by UV–visible wavelength scans and nanoparticle tracking analysis. Nanoparticles could be synthesized in reproducible yields of approximately 10(8) particles/ml with mode particles sizes of approx. 90–100 nm. Antibacterial activity against two pathogens was assessed by minimal inhibitory concentration assays and survival curves. Both pathogens exhibited similar resistance profiles with minimal inhibitory concentrations ranging between 5 × 10(5) and 10(7) particles/ml. Interestingly, zinc nanoparticles showed a slightly higher efficacy, but sublethal concentrations caused adverse effects and resulted in increased biofilm formation of V. cholerae. Using the expression levels of the outer membrane porin OmpT as an indicator for cAMP levels, our results suggest that zinc nanoparticles inhibit adenylyl cyclase activity. This consequently deceases the levels of this second messenger, which is a known inhibitor of biofilm formation. Finally, we demonstrated that a single oral administration of silver nanoparticles to infant mice colonized with V. cholerae or ETEC significantly reduces the colonization rates of the pathogens by 75- or 100-fold, respectively.
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spelling pubmed-43004262015-01-23 Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli Salem, Wesam Leitner, Deborah R. Zingl, Franz G. Schratter, Gebhart Prassl, Ruth Goessler, Walter Reidl, Joachim Schild, Stefan Int J Med Microbiol Article Vibrio cholerae and enterotoxic Escherichia coli (ETEC) remain two dominant bacterial causes of severe secretory diarrhea and still a significant cause of death, especially in developing countries. In order to investigate new effective and inexpensive therapeutic approaches, we analyzed nanoparticles synthesized by a green approach using corresponding salt (silver or zinc nitrate) with aqueous extract of Caltropis procera fruit or leaves. We characterized the quantity and quality of nanoparticles by UV–visible wavelength scans and nanoparticle tracking analysis. Nanoparticles could be synthesized in reproducible yields of approximately 10(8) particles/ml with mode particles sizes of approx. 90–100 nm. Antibacterial activity against two pathogens was assessed by minimal inhibitory concentration assays and survival curves. Both pathogens exhibited similar resistance profiles with minimal inhibitory concentrations ranging between 5 × 10(5) and 10(7) particles/ml. Interestingly, zinc nanoparticles showed a slightly higher efficacy, but sublethal concentrations caused adverse effects and resulted in increased biofilm formation of V. cholerae. Using the expression levels of the outer membrane porin OmpT as an indicator for cAMP levels, our results suggest that zinc nanoparticles inhibit adenylyl cyclase activity. This consequently deceases the levels of this second messenger, which is a known inhibitor of biofilm formation. Finally, we demonstrated that a single oral administration of silver nanoparticles to infant mice colonized with V. cholerae or ETEC significantly reduces the colonization rates of the pathogens by 75- or 100-fold, respectively. Urban & Fischer Verlag 2015-01 /pmc/articles/PMC4300426/ /pubmed/25466205 http://dx.doi.org/10.1016/j.ijmm.2014.11.005 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Salem, Wesam
Leitner, Deborah R.
Zingl, Franz G.
Schratter, Gebhart
Prassl, Ruth
Goessler, Walter
Reidl, Joachim
Schild, Stefan
Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli
title Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli
title_full Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli
title_fullStr Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli
title_full_unstemmed Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli
title_short Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli
title_sort antibacterial activity of silver and zinc nanoparticles against vibrio cholerae and enterotoxic escherichia coli
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300426/
https://www.ncbi.nlm.nih.gov/pubmed/25466205
http://dx.doi.org/10.1016/j.ijmm.2014.11.005
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