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Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates
BACKGROUND: This article examines the use of a novel nano-system, gold nanoparticles coated with indolicidin (AuNPs–indolicidin), against pathogenic Candida albicans biofilms. Candida species cause frequent infections owing to their ability to form biofilms, primarily on implant devices. MATERIALS A...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037145/ https://www.ncbi.nlm.nih.gov/pubmed/30013374 http://dx.doi.org/10.2147/IDR.S164262 |
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author | de Alteriis, Elisabetta Maselli, Valeria Falanga, Annarita Galdiero, Stefania Di Lella, Federica Maria Gesuele, Renato Guida, Marco Galdiero, Emilia |
author_facet | de Alteriis, Elisabetta Maselli, Valeria Falanga, Annarita Galdiero, Stefania Di Lella, Federica Maria Gesuele, Renato Guida, Marco Galdiero, Emilia |
author_sort | de Alteriis, Elisabetta |
collection | PubMed |
description | BACKGROUND: This article examines the use of a novel nano-system, gold nanoparticles coated with indolicidin (AuNPs–indolicidin), against pathogenic Candida albicans biofilms. Candida species cause frequent infections owing to their ability to form biofilms, primarily on implant devices. MATERIALS AND METHODS: We used an integrated approach, evaluating the effect of AuNPs-indolicidin on prevention and eradication of Candida biofilms formed in multi-well polystyrene plates, with relative gene expression assays. Four biofilm-associated genes (FG1, HWP1, ALS1 and ALS3, and CDR1 and CDR2) involved in efflux pump were analyzed using reverse transcription polymerase chain reaction. RESULTS: Treatment with the nano-complex significantly inhibits the capacity of C. albicans to form biofilms and impairs preformed mature biofilms. Treatment with AuNPs–indolicidin results in an increase in the kinetics of Rhodamine 6G efflux and a reduction in the expression of biofilm-related genes. CONCLUSION: These data provide a chance to develop novel therapies against nosocomially acquired refractory C. albicans biofilms. |
format | Online Article Text |
id | pubmed-6037145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60371452018-07-16 Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates de Alteriis, Elisabetta Maselli, Valeria Falanga, Annarita Galdiero, Stefania Di Lella, Federica Maria Gesuele, Renato Guida, Marco Galdiero, Emilia Infect Drug Resist Original Research BACKGROUND: This article examines the use of a novel nano-system, gold nanoparticles coated with indolicidin (AuNPs–indolicidin), against pathogenic Candida albicans biofilms. Candida species cause frequent infections owing to their ability to form biofilms, primarily on implant devices. MATERIALS AND METHODS: We used an integrated approach, evaluating the effect of AuNPs-indolicidin on prevention and eradication of Candida biofilms formed in multi-well polystyrene plates, with relative gene expression assays. Four biofilm-associated genes (FG1, HWP1, ALS1 and ALS3, and CDR1 and CDR2) involved in efflux pump were analyzed using reverse transcription polymerase chain reaction. RESULTS: Treatment with the nano-complex significantly inhibits the capacity of C. albicans to form biofilms and impairs preformed mature biofilms. Treatment with AuNPs–indolicidin results in an increase in the kinetics of Rhodamine 6G efflux and a reduction in the expression of biofilm-related genes. CONCLUSION: These data provide a chance to develop novel therapies against nosocomially acquired refractory C. albicans biofilms. Dove Medical Press 2018-07-03 /pmc/articles/PMC6037145/ /pubmed/30013374 http://dx.doi.org/10.2147/IDR.S164262 Text en © 2018 de Altariis et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research de Alteriis, Elisabetta Maselli, Valeria Falanga, Annarita Galdiero, Stefania Di Lella, Federica Maria Gesuele, Renato Guida, Marco Galdiero, Emilia Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates |
title | Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates |
title_full | Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates |
title_fullStr | Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates |
title_full_unstemmed | Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates |
title_short | Efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of Candida spp. clinical isolates |
title_sort | efficiency of gold nanoparticles coated with the antimicrobial peptide indolicidin against biofilm formation and development of candida spp. clinical isolates |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037145/ https://www.ncbi.nlm.nih.gov/pubmed/30013374 http://dx.doi.org/10.2147/IDR.S164262 |
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