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Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study

BACKGROUND: Candida albicans is the most common pathogenic fungus isolated in bloodstream infections in hospitalized patients, and candidiasis represents the fourth most common infection in United States hospitals, mostly due to the increasing numbers of immune- and medically-compromised patients. C...

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Autores principales: Lara, Humberto H., Romero-Urbina, Dulce G., Pierce, Christopher, Lopez-Ribot, Jose L., Arellano-Jiménez, M. Josefina, Jose-Yacaman, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678641/
https://www.ncbi.nlm.nih.gov/pubmed/26666378
http://dx.doi.org/10.1186/s12951-015-0147-8
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author Lara, Humberto H.
Romero-Urbina, Dulce G.
Pierce, Christopher
Lopez-Ribot, Jose L.
Arellano-Jiménez, M. Josefina
Jose-Yacaman, Miguel
author_facet Lara, Humberto H.
Romero-Urbina, Dulce G.
Pierce, Christopher
Lopez-Ribot, Jose L.
Arellano-Jiménez, M. Josefina
Jose-Yacaman, Miguel
author_sort Lara, Humberto H.
collection PubMed
description BACKGROUND: Candida albicans is the most common pathogenic fungus isolated in bloodstream infections in hospitalized patients, and candidiasis represents the fourth most common infection in United States hospitals, mostly due to the increasing numbers of immune- and medically-compromised patients. C. albicans has the ability to form biofilms and morphogenetic conversions between yeast and hyphal morphologies contribute to biofilm development and represent an essential virulence factor. Moreover, these attached communities of cells are surrounded by a protective exopolymeric matrix that effectively shelters Candida against the action of antifungals. Because of dismal outcomes, novel antifungal strategies, and in particular those targeting biofilms are urgently required. As fungi are eukaryotic, research and development of new antifungal agents has been difficult due to the limited number of selective targets, also leading to toxicity. RESULTS: By microwave-assisted techniques we obtained pure 1 nm spherical silver nanoparticles ideal for their potential biological applications without adding contaminants. A phenotypic assay of C. albicans demonstrated a potent dose-dependent inhibitory effect of silver nanoparticles on biofilm formation, with an IC(50) of 0.089 ppm. Also silver nanoparticles demonstrated efficacy when tested against pre-formed C. albicans biofilms resulting in an IC(50) of 0.48 ppm. The cytotoxicity assay resulted in a CC(50) of 7.03 ppm. The ultrastructural differences visualized under SEM with silver nanoparticles treatment were changes in the surface appearance of the yeast from smooth to rough thus indicating outer cell wall damage. On the fungal pre-formed biofilm true hyphae was mostly absent, as filamentation was inhibited. TEM measurement of the cell-wall width of C. albicans after treatment resulted in significant enlargement (206  ±  11 nm) demonstrating membrane permeabilization. CONCLUSIONS: Our results demonstrate that silver nanoparticles are potent inhibitors of C. albicans biofilm formation. SEM observations are consistent with an overall loss of structure of biofilms mostly due to disruption of the outer cell membrane/wall and inhibition of filamentation.TEM indicates the permeabilization of the cell wall and subsequent disruption of the structural layers of the outer fungal cell wall. The anti-biofilm effects are via cell wall disruption. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-015-0147-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-46786412015-12-16 Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study Lara, Humberto H. Romero-Urbina, Dulce G. Pierce, Christopher Lopez-Ribot, Jose L. Arellano-Jiménez, M. Josefina Jose-Yacaman, Miguel J Nanobiotechnology Research BACKGROUND: Candida albicans is the most common pathogenic fungus isolated in bloodstream infections in hospitalized patients, and candidiasis represents the fourth most common infection in United States hospitals, mostly due to the increasing numbers of immune- and medically-compromised patients. C. albicans has the ability to form biofilms and morphogenetic conversions between yeast and hyphal morphologies contribute to biofilm development and represent an essential virulence factor. Moreover, these attached communities of cells are surrounded by a protective exopolymeric matrix that effectively shelters Candida against the action of antifungals. Because of dismal outcomes, novel antifungal strategies, and in particular those targeting biofilms are urgently required. As fungi are eukaryotic, research and development of new antifungal agents has been difficult due to the limited number of selective targets, also leading to toxicity. RESULTS: By microwave-assisted techniques we obtained pure 1 nm spherical silver nanoparticles ideal for their potential biological applications without adding contaminants. A phenotypic assay of C. albicans demonstrated a potent dose-dependent inhibitory effect of silver nanoparticles on biofilm formation, with an IC(50) of 0.089 ppm. Also silver nanoparticles demonstrated efficacy when tested against pre-formed C. albicans biofilms resulting in an IC(50) of 0.48 ppm. The cytotoxicity assay resulted in a CC(50) of 7.03 ppm. The ultrastructural differences visualized under SEM with silver nanoparticles treatment were changes in the surface appearance of the yeast from smooth to rough thus indicating outer cell wall damage. On the fungal pre-formed biofilm true hyphae was mostly absent, as filamentation was inhibited. TEM measurement of the cell-wall width of C. albicans after treatment resulted in significant enlargement (206  ±  11 nm) demonstrating membrane permeabilization. CONCLUSIONS: Our results demonstrate that silver nanoparticles are potent inhibitors of C. albicans biofilm formation. SEM observations are consistent with an overall loss of structure of biofilms mostly due to disruption of the outer cell membrane/wall and inhibition of filamentation.TEM indicates the permeabilization of the cell wall and subsequent disruption of the structural layers of the outer fungal cell wall. The anti-biofilm effects are via cell wall disruption. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-015-0147-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-15 /pmc/articles/PMC4678641/ /pubmed/26666378 http://dx.doi.org/10.1186/s12951-015-0147-8 Text en © Lara et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lara, Humberto H.
Romero-Urbina, Dulce G.
Pierce, Christopher
Lopez-Ribot, Jose L.
Arellano-Jiménez, M. Josefina
Jose-Yacaman, Miguel
Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study
title Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study
title_full Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study
title_fullStr Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study
title_full_unstemmed Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study
title_short Effect of silver nanoparticles on Candida albicans biofilms: an ultrastructural study
title_sort effect of silver nanoparticles on candida albicans biofilms: an ultrastructural study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678641/
https://www.ncbi.nlm.nih.gov/pubmed/26666378
http://dx.doi.org/10.1186/s12951-015-0147-8
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