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

Detalhes bibliográficos
Autor(a) principal: Parreira, P
Data de Publicação: 2019
Outros Autores: Monteiro, C, Graça, V, Gomes, J, Maia, S, Gomes, P, Gonçalves, IC, Martins, MCL
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/138981
Resumo: 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/cm2 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 Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection ManagementAs 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/cm2 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 Group20192019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/138981eng2045-232210.1038/s41598-019-53918-4Parreira, PMonteiro, CGraça, VGomes, JMaia, SGomes, PGonçalves, ICMartins, MCLinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T12:44:15Zoai:repositorio-aberto.up.pt:10216/138981Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:25:43.383927Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv 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
spellingShingle Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
Parreira, P
title_short 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_sort Surface Grafted MSI-78A Antimicrobial Peptide has High Potential for Gastric Infection Management
author Parreira, P
author_facet Parreira, P
Monteiro, C
Graça, V
Gomes, J
Maia, S
Gomes, P
Gonçalves, IC
Martins, MCL
author_role author
author2 Monteiro, C
Graça, V
Gomes, J
Maia, S
Gomes, P
Gonçalves, IC
Martins, MCL
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Parreira, P
Monteiro, C
Graça, V
Gomes, J
Maia, S
Gomes, P
Gonçalves, IC
Martins, MCL
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/cm2 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.
publishDate 2019
dc.date.none.fl_str_mv 2019
2019-01-01T00:00:00Z
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10.1038/s41598-019-53918-4
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