Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers

New anti-infective materials are needed urgently as alternatives to conventional biocides. It has recently been established that polymer materials designed to bind to the surface of bacteria can induce the formation of cell clusters which enhance the expression of quorum sensing controlled phenotype...

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Main Authors: Louzao, Iria, Sui, Cheng, Winzer, Klaus, Fernandez-Trillo, Francisco, Alexander, Cameron
Format: Article
Published: Elsevier 2015
Subjects:
Online Access:https://eprints.nottingham.ac.uk/39064/
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author Louzao, Iria
Sui, Cheng
Winzer, Klaus
Fernandez-Trillo, Francisco
Alexander, Cameron
author_facet Louzao, Iria
Sui, Cheng
Winzer, Klaus
Fernandez-Trillo, Francisco
Alexander, Cameron
author_sort Louzao, Iria
building Nottingham Research Data Repository
collection Online Access
description New anti-infective materials are needed urgently as alternatives to conventional biocides. It has recently been established that polymer materials designed to bind to the surface of bacteria can induce the formation of cell clusters which enhance the expression of quorum sensing controlled phenotypes. These materials are relevant for anti-infective strategies as they have the potential to inhibit adhesion while at the same time modulating Quorum Sensing (QS) controlled virulence. Here we carefully evaluate the role that charge and catechol moieties in these polymers play on the binding. We investigate the ability of the cationic polymers poly(N-[3-(dimethylamino)propyl] methacrylamide) (pDMAPMAm, P1), poly(N-dopamine methacrylamide-co-N-[3-(dimethylamino)propyl] methacrylamide) (pDMAm-co-pDMAPMAm, P2) and p(3,4-dihydroxy-l-phenylalanine methacrylamide), p(l-DMAm, P3) to cluster a range of bacteria, such as Staphylococcus aureus (Gram-positive), Vibrio harveyi, Escherichia coli and Pseudomonas aeruginosa (Gram-negative) under conditions of varying pH (6, 7 and 8) and polymer concentration (0.1 and 0.5 mg/mL). We identify that clustering ability is strongly dependent on the balance between charge and hydrophobicity. Moreover, our results suggest that catechol moieties have a positive effect on adhesive properties, but only in the presence of cationic residues such as for P2. Overall, our results highlight the subtle interplay between dynamic natural surfaces and synthetic materials, as well as the need to consider synergistic structure–property relationship when designing antimicrobial polymers.
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spelling nottingham-390642020-05-04T20:07:19Z https://eprints.nottingham.ac.uk/39064/ Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers Louzao, Iria Sui, Cheng Winzer, Klaus Fernandez-Trillo, Francisco Alexander, Cameron New anti-infective materials are needed urgently as alternatives to conventional biocides. It has recently been established that polymer materials designed to bind to the surface of bacteria can induce the formation of cell clusters which enhance the expression of quorum sensing controlled phenotypes. These materials are relevant for anti-infective strategies as they have the potential to inhibit adhesion while at the same time modulating Quorum Sensing (QS) controlled virulence. Here we carefully evaluate the role that charge and catechol moieties in these polymers play on the binding. We investigate the ability of the cationic polymers poly(N-[3-(dimethylamino)propyl] methacrylamide) (pDMAPMAm, P1), poly(N-dopamine methacrylamide-co-N-[3-(dimethylamino)propyl] methacrylamide) (pDMAm-co-pDMAPMAm, P2) and p(3,4-dihydroxy-l-phenylalanine methacrylamide), p(l-DMAm, P3) to cluster a range of bacteria, such as Staphylococcus aureus (Gram-positive), Vibrio harveyi, Escherichia coli and Pseudomonas aeruginosa (Gram-negative) under conditions of varying pH (6, 7 and 8) and polymer concentration (0.1 and 0.5 mg/mL). We identify that clustering ability is strongly dependent on the balance between charge and hydrophobicity. Moreover, our results suggest that catechol moieties have a positive effect on adhesive properties, but only in the presence of cationic residues such as for P2. Overall, our results highlight the subtle interplay between dynamic natural surfaces and synthetic materials, as well as the need to consider synergistic structure–property relationship when designing antimicrobial polymers. Elsevier 2015-09 Article PeerReviewed Louzao, Iria, Sui, Cheng, Winzer, Klaus, Fernandez-Trillo, Francisco and Alexander, Cameron (2015) Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers. European Journal of Pharmaceutics and Biopharmaceutics, 95 . pp. 47-62. ISSN 1873-3441 Polymers; Gram-positive and gram-negative bacteria; Anti-infective materials; Adhesion; Polycations; Catechols http://www.sciencedirect.com/science/article/pii/S0939641115002581 doi:10.1016/j.ejpb.2015.05.026 doi:10.1016/j.ejpb.2015.05.026
spellingShingle Polymers; Gram-positive and gram-negative bacteria; Anti-infective materials; Adhesion; Polycations; Catechols
Louzao, Iria
Sui, Cheng
Winzer, Klaus
Fernandez-Trillo, Francisco
Alexander, Cameron
Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers
title Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers
title_full Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers
title_fullStr Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers
title_full_unstemmed Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers
title_short Cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers
title_sort cationic polymer mediated bacterial clustering: cell-adhesive properties of homo- and copolymers
topic Polymers; Gram-positive and gram-negative bacteria; Anti-infective materials; Adhesion; Polycations; Catechols
url https://eprints.nottingham.ac.uk/39064/
https://eprints.nottingham.ac.uk/39064/
https://eprints.nottingham.ac.uk/39064/