Author(s):
Alves, D. ; Sileika, Tadas ; Messersmith, Phillip ; Pereira, Maria Olívia
Date: 2016
Persistent ID: http://hdl.handle.net/1822/42544
Origin: RepositóriUM - Universidade do Minho
Project/scholarship:
info:eu-repo/grantAgreement/FCT/5876/147337/PT;
info:eu-repo/grantAgreement/FCT/5876-PPCDTI/113196/PT
;
info:eu-repo/grantAgreement/FCT/5876-PPCDTI/126270/PT
;
info:eu-repo/grantAgreement/FCT/COMPETE/126270/PT;
Subject(s): Funcionalization of polycarbonate surfaces with alginate lyase; Dopamine-based coating strategy; Antiadhesion surfaces; Catalysis-independent performance; alginate lyase; antibacterial coating; catalysis-independent; dopamine chemistry; Science & Technology
Description
Given alginate’s contribution to Pseudomonas aeruginosa virulence, it has long been considered a promising target for interventional therapies, which have been performed by using the enzyme alginate lyase. In this work, instead of treating pre-established mucoid biofi lms, alginate lyase is immobilized onto a surface as a preventive measure against P. aeruginosa adhesion. A polydopamine dip-coating strategy is employed for functionalization of polycarbonate surfaces. Enzyme immobilization is confi rmed by surface characterization. Surfaces functionalized with alginate lyase exhibit anti-adhesive properties, inhibiting the attachment of the mucoid strain. Moreover, surfaces modifi ed with this enzyme also inhibit the adhesion of the tested non-mucoid strain. Unexpectedly, treatment with heat-inactivated enzyme also inhibits the attachment of mucoid and non-mucoid P. aeruginosa strains. These fi ndings suggest that the antibacterial performance of alginate lyase functional coatings is catalysis-independent, highlighting the importance of further studies to better understand its mechanism of action against P. aeruginosa strains.
T he authors acknowledge the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit and COMPETE 2020 (POCI-01-0145-FEDER-006684). This study was also supported by FCT and the European Community fund FEDER, through Program COMPETE, under the scope of the Projects “PTDC/SAU-SAP/113196/2009” (FCOMP-01-0124-FEDER-016012) and “RECI/BBB-EBI/0179/2012” (FCOMP-01-0124-FEDER-027462). The authors also acknowledge Dr. Margarida Martins from 3B’s Research Group – Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine (AvePark, 4806-909 Taipas/Guimarãe s, Portugal) for kindly providing the isolated strains which were obtained under the scope of the project “Insights into peritoneal dialysis catheter associated biofi lms” funded by the Portuguese Society of Nephrology to Dr. Anabela Rodrigues. The authors also acknowledge the Ph.D. Grant of Diana Alves (SFRH/BD/78063/2011). T.S.S. was funded by a National Science Foundation graduate fellowship (Grant No. GRFP 2011124091), the Ryan Fellowship of Northwestern University, and NIH grant R37 DE014193 to P.B.M.
