Cargando…

Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa

PURPOSE: To determine the antimicrobial activity of poly-epsilon-lysine (pɛK) functionalization of hydrogels against Pseudomonas aeruginosa. METHODS: Antimicrobial activities of pɛK and pɛK+ hydrogels were tested against both keratitis and a laboratory strain of P aeruginosa at a range of inocula si...

Descripción completa

Detalles Bibliográficos
Autores principales: Kennedy, Stephnie M., Deshpande, Pallavi, Gallagher, Andrew G., Horsburgh, Malcolm J., Allison, Heather E., Kaye, Stephen B., Wellings, Donald A., Williams, Rachel L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441358/
https://www.ncbi.nlm.nih.gov/pubmed/32776141
http://dx.doi.org/10.1167/iovs.61.10.18
_version_ 1783573280403226624
author Kennedy, Stephnie M.
Deshpande, Pallavi
Gallagher, Andrew G.
Horsburgh, Malcolm J.
Allison, Heather E.
Kaye, Stephen B.
Wellings, Donald A.
Williams, Rachel L.
author_facet Kennedy, Stephnie M.
Deshpande, Pallavi
Gallagher, Andrew G.
Horsburgh, Malcolm J.
Allison, Heather E.
Kaye, Stephen B.
Wellings, Donald A.
Williams, Rachel L.
author_sort Kennedy, Stephnie M.
collection PubMed
description PURPOSE: To determine the antimicrobial activity of poly-epsilon-lysine (pɛK) functionalization of hydrogels against Pseudomonas aeruginosa. METHODS: Antimicrobial activities of pɛK and pɛK+ hydrogels were tested against both keratitis and a laboratory strain of P aeruginosa at a range of inocula sizes, over 4 and 24 hours. The number of viable CFU on pɛK and pɛK+ hydrogels or commercial contact lenses (CL) was investigated. Ex vivo porcine corneas were inoculated with P aeruginosa PAO1 (10(3) CFU) and incubated with pɛK+ hydrogels or commercial hydrogel CL for 24 hours and the effects of infection determined. RESULTS: PɛK+ hydrogels showed log reductions in viable CFU compared with pɛK hydrogels for all P aeruginosa strains, depending on inocula sizes and incubation time. After 24 hours pɛK+ hydrogels showed >5 and >7.5 log reduction in CFU compared with commercial hydrogel CL at 10(3) and 10(6) CFU, respectively. In an ex vivo porcine corneal infection model, pɛK+ hydrogels led to a significant decrease in viable PAO1 CFU and histologic analysis indicated a decreased infiltration of PAO1 into the stroma. CONCLUSIONS: PɛK+ hydrogels demonstrated enhanced antimicrobial activity versus nonfunctionalized pɛK hydrogels against clinically relevant P aeruginosa strains. PɛK+ hydrogels have the potential to be used as a bandage CL with innate antimicrobial characteristics to minimize the risk of microbial keratitis.
format Online
Article
Text
id pubmed-7441358
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Association for Research in Vision and Ophthalmology
record_format MEDLINE/PubMed
spelling pubmed-74413582020-08-31 Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa Kennedy, Stephnie M. Deshpande, Pallavi Gallagher, Andrew G. Horsburgh, Malcolm J. Allison, Heather E. Kaye, Stephen B. Wellings, Donald A. Williams, Rachel L. Invest Ophthalmol Vis Sci Immunology and Microbiology PURPOSE: To determine the antimicrobial activity of poly-epsilon-lysine (pɛK) functionalization of hydrogels against Pseudomonas aeruginosa. METHODS: Antimicrobial activities of pɛK and pɛK+ hydrogels were tested against both keratitis and a laboratory strain of P aeruginosa at a range of inocula sizes, over 4 and 24 hours. The number of viable CFU on pɛK and pɛK+ hydrogels or commercial contact lenses (CL) was investigated. Ex vivo porcine corneas were inoculated with P aeruginosa PAO1 (10(3) CFU) and incubated with pɛK+ hydrogels or commercial hydrogel CL for 24 hours and the effects of infection determined. RESULTS: PɛK+ hydrogels showed log reductions in viable CFU compared with pɛK hydrogels for all P aeruginosa strains, depending on inocula sizes and incubation time. After 24 hours pɛK+ hydrogels showed >5 and >7.5 log reduction in CFU compared with commercial hydrogel CL at 10(3) and 10(6) CFU, respectively. In an ex vivo porcine corneal infection model, pɛK+ hydrogels led to a significant decrease in viable PAO1 CFU and histologic analysis indicated a decreased infiltration of PAO1 into the stroma. CONCLUSIONS: PɛK+ hydrogels demonstrated enhanced antimicrobial activity versus nonfunctionalized pɛK hydrogels against clinically relevant P aeruginosa strains. PɛK+ hydrogels have the potential to be used as a bandage CL with innate antimicrobial characteristics to minimize the risk of microbial keratitis. The Association for Research in Vision and Ophthalmology 2020-08-10 /pmc/articles/PMC7441358/ /pubmed/32776141 http://dx.doi.org/10.1167/iovs.61.10.18 Text en Copyright 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Immunology and Microbiology
Kennedy, Stephnie M.
Deshpande, Pallavi
Gallagher, Andrew G.
Horsburgh, Malcolm J.
Allison, Heather E.
Kaye, Stephen B.
Wellings, Donald A.
Williams, Rachel L.
Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa
title Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa
title_full Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa
title_fullStr Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa
title_full_unstemmed Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa
title_short Antimicrobial Activity of Poly-epsilon-lysine Peptide Hydrogels Against Pseudomonas aeruginosa
title_sort antimicrobial activity of poly-epsilon-lysine peptide hydrogels against pseudomonas aeruginosa
topic Immunology and Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441358/
https://www.ncbi.nlm.nih.gov/pubmed/32776141
http://dx.doi.org/10.1167/iovs.61.10.18
work_keys_str_mv AT kennedystephniem antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa
AT deshpandepallavi antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa
AT gallagherandrewg antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa
AT horsburghmalcolmj antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa
AT allisonheathere antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa
AT kayestephenb antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa
AT wellingsdonalda antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa
AT williamsrachell antimicrobialactivityofpolyepsilonlysinepeptidehydrogelsagainstpseudomonasaeruginosa