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Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management

As we approach the end of the antibiotic era, newer therapeutic options, such as antimicrobial peptides (AMPs), are in urgent demand. AMP surface grafting onto biomaterials has been described as a good strategy to overcome problems associated with their in vivo stability. Helicobacter pylori is amon...

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Autores principales: Parreira, Paula, Monteiro, Claudia, Graça, Vanessa, Gomes, Joana, Maia, Sílvia, Gomes, Paula, Gonçalves, Inês C., Martins, M. Cristina L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890677/
https://www.ncbi.nlm.nih.gov/pubmed/31796755
http://dx.doi.org/10.1038/s41598-019-53918-4
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author Parreira, Paula
Monteiro, Claudia
Graça, Vanessa
Gomes, Joana
Maia, Sílvia
Gomes, Paula
Gonçalves, Inês C.
Martins, M. Cristina L.
author_facet Parreira, Paula
Monteiro, Claudia
Graça, Vanessa
Gomes, Joana
Maia, Sílvia
Gomes, Paula
Gonçalves, Inês C.
Martins, M. Cristina L.
author_sort Parreira, Paula
collection PubMed
description As we approach the end of the antibiotic era, newer therapeutic options, such as antimicrobial peptides (AMPs), are in urgent demand. AMP surface grafting onto biomaterials has been described as a good strategy to overcome problems associated with their in vivo stability. Helicobacter pylori is among the bacteria that pose greatest threat to human health, being MSI-78A one of the few bactericidal AMPs against this bacterium. Here, we report that MSI-78A grafted onto model surfaces (Self-Assembled Monolayers –SAMs), in a concentration of 30.3 ± 1.2 ng/cm(2) determined by quartz crystal microbalance with dissipation (QCM-D), was able to kill, by contact, 98% of planktonic H. pylori in only 2 h. This fact was not verified against the control bacteria (Staphylococcus epidermidis), although the minimal inhibitory concentration (MIC) of MSI-78A in solution is much lower for S. epidermidis (2 μg/mL) than for H. pylori (64 μg/mL). Our results also demonstrated that, in opposite to other bacteria, H. pylori cells were attracted to ethylene glycol terminated (antiadhesive) surfaces, which can explain the high bactericidal potential of grafted MSI-78A. This proof of concept study establishes the foundations for development of MSI-78A grafted nanoparticles for gastric infection management within a targeted nanomedicine concept.
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spelling pubmed-68906772019-12-10 Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management Parreira, Paula Monteiro, Claudia Graça, Vanessa Gomes, Joana Maia, Sílvia Gomes, Paula Gonçalves, Inês C. Martins, M. Cristina L. Sci Rep Article As we approach the end of the antibiotic era, newer therapeutic options, such as antimicrobial peptides (AMPs), are in urgent demand. AMP surface grafting onto biomaterials has been described as a good strategy to overcome problems associated with their in vivo stability. Helicobacter pylori is among the bacteria that pose greatest threat to human health, being MSI-78A one of the few bactericidal AMPs against this bacterium. Here, we report that MSI-78A grafted onto model surfaces (Self-Assembled Monolayers –SAMs), in a concentration of 30.3 ± 1.2 ng/cm(2) determined by quartz crystal microbalance with dissipation (QCM-D), was able to kill, by contact, 98% of planktonic H. pylori in only 2 h. This fact was not verified against the control bacteria (Staphylococcus epidermidis), although the minimal inhibitory concentration (MIC) of MSI-78A in solution is much lower for S. epidermidis (2 μg/mL) than for H. pylori (64 μg/mL). Our results also demonstrated that, in opposite to other bacteria, H. pylori cells were attracted to ethylene glycol terminated (antiadhesive) surfaces, which can explain the high bactericidal potential of grafted MSI-78A. This proof of concept study establishes the foundations for development of MSI-78A grafted nanoparticles for gastric infection management within a targeted nanomedicine concept. Nature Publishing Group UK 2019-12-03 /pmc/articles/PMC6890677/ /pubmed/31796755 http://dx.doi.org/10.1038/s41598-019-53918-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Parreira, Paula
Monteiro, Claudia
Graça, Vanessa
Gomes, Joana
Maia, Sílvia
Gomes, Paula
Gonçalves, Inês C.
Martins, M. Cristina L.
Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
title Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
title_full Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
title_fullStr Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
title_full_unstemmed Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
title_short Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
title_sort surface grafted msi-78a antimicrobial peptide has high potential for gastric infection management
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890677/
https://www.ncbi.nlm.nih.gov/pubmed/31796755
http://dx.doi.org/10.1038/s41598-019-53918-4
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