Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/163455
Author(s): Costa, B
Coelho, J
Silva, V
Shahrour, H
Costa, NA
Ribeiro, AR
Santos, SG
Costa, F
Martínez-de-Tejada, G
Monteiro, C
Martins, MCL
Title: Dhvar5- and MSI78-coated titanium are bactericidal against methicillin-resistant Staphylococcus aureus, immunomodulatory and osteogenic
Publisher: Elsevier
Issue Date: 2024
Abstract: Infection is one of the major issues associated with the failure of orthopedic devices, mainly due to implant bacterial colonization, biofilm formation, and associated antibiotic resistance. Antimicrobial peptides (AMP) are a promising alternative to conventional antibiotics given their broad-spectrum of activity, low propensity to induce bacterial resistance, and ability to modulate host immune responses. Dhvar5 (LLLFLLKKRKKRKY) and MSI78 (GIGKFLKKAKKFGKAFVKILKK) are two AMP with broad-spectrum activity against bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), one of the most problematic etiologic agents in Orthopedic Devices-Related Infections (ODRI). This work aims to evaluate the bactericidal, immunomodulatory and osteogenic potential of Dhvar5- and MSI78-coated titanium surfaces (AMP-Ti). Two AMP-Ti surfaces were successfully obtained by grafting Dhvar5 (0.8 ± 0.1 µM/mm2) or MSI78 (0.5 ± 0.3 µM/mm2) onto titanium substrates through a polydopamine layer. Both AMP-Ti were bactericidal against MRSA, eradicating bacteria upon contact for 6 h in a culture medium supplemented with human plasma proteins. The AMP-Ti immunomodulatory potential was evaluated using human primary macrophages, by assessing surfaces capacity to induce pro-/anti-inflammatory (M1/M2) markers and cytokines. While in naïve conditions both AMP-Ti surfaces slightly promoted the M2 marker CD163, in response to LPS and IFN-γ (simulating a bacterial infection), both AMP increased the M1 marker CCR7 and enhanced macrophage secretion of pro-inflammatory IL-6 and TNF-α cytokines, particularly for Ti-MSI78 surfaces. Additionally, both AMP-Ti surfaces were cytocompatible and promoted osteoblastic cell differentiation. This proof-of-concept study demonstrated the high potential of Dhvar5- and MSI78-Ti as antimicrobial coatings for ODRI prevention. STATEMENT OF SIGNIFICANCE: This study investigates the bactericidal effects of the antimicrobial peptides Dhvar5 and MSI78, immobilized on titanium (Ti) surfaces through a polydopamine coating, aiming at the prevention of Orthopedic-Device Related Infections (ODRIs). The developed coatings displayed MRSA-sterilizing activity, while revealing an immunomodulatory potential towards macrophages and promoting osteoblastic cell differentiation. This strategy allows a quick and easy immobilization of high quantities of AMP, unlike most other approaches, thus favoring its clinical translation.
Description: This work was financed by Portuguese funds through FCT-Fundaç˜ao para a Ciˆencia e a Tecnologia/Minist´erio da Ciˆencia, Tecnologia e Inovaç˜ao in the framework of the grants/contracts for Bruna Costa (SFRH/BD/147,027/2019), Joana Coelho (2023.03848.BD), Fabíola Costa (CEECIND/01921/2017), Cl´audia Monteiro (art. 23 of Law no. 57/2016 & 57/2017) and M. Cristina L. Martins (LA/P/0070/2020). Nat´alia A. Costa thanks to Coordenaç˜ao de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) - Finance Codes 88887.600413/ 2021–00 and 88887.802752/2023–00, and S˜ao Paulo Research Foundation (FAPESP) (grants #2020/10125–9 and #2021/11461–5). M. Cristina L. Martins also acknowledges MOBILIsE Project, which has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement no. 951,723. XPS analysis was funded by the European Union’s H2020 project Sinfonia (N.857253).
Subject: Antibacterial activity
Antimicrobial peptides
Dopamine
Immunomodulation
Macrophages
Surface immobilization
DOI: 10.1016/j.actbio.2024.11.016
URI: https://hdl.handle.net/10216/163455
Series: Acta biomaterialia
Related Information: info:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBD%2F147027%2F2019/PT
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/LA%2FP%2F0070%2F2020/PT
info:eu-repo/grantAgreement/EC/H2020/951723/EU
info:eu-repo/grantAgreement/EC/H2020/857253/EU
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: https://creativecommons.org/licenses/by/4.0/
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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