Efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds

Novel anti-biofilm and dispersal agents are currently being investigated in an attempt to combat biofilm-associated wound infections. Glycoside hydrolases (GHs) are enzymes that hydrolyze the glycosidic bonds between sugars, such as those found within the exopolysaccharides of the biofilm matrix. Pr...

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Autores principales: Whitni K. Redman, Garrett S. Welch, Avery C. Williams, Addyson J. Damron, Willem O. Northcut, Kendra P. Rumbaugh
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Publicado: Elsevier 2021
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spelling oai:doaj.org-article:00006f095d0046cabafe5a1f55b5ab542021-11-18T04:51:29ZEfficacy and safety of biofilm dispersal by glycoside hydrolases in wounds2590-207510.1016/j.bioflm.2021.100061https://doaj.org/article/00006f095d0046cabafe5a1f55b5ab542021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2590207521000198https://doaj.org/toc/2590-2075Novel anti-biofilm and dispersal agents are currently being investigated in an attempt to combat biofilm-associated wound infections. Glycoside hydrolases (GHs) are enzymes that hydrolyze the glycosidic bonds between sugars, such as those found within the exopolysaccharides of the biofilm matrix. Previous studies have shown that GHs can weaken the matrix, inducing bacterial dispersal, and improving antibiotic clearance. Yet, the number of GH enzymes that have been examined for potential therapeutic effects is limited. In this study, we screened sixteen GHs for their ability to disperse mono-microbial and polymicrobial biofilms grown in different environments. Six GHs, α-amylase (source: A. oryzae), alginate lyase (source: various algae), pectinase (source: Rhizopus sp.), amyloglucosidase (source: A. niger), inulinase (source: A. niger), and xylanase (source: A. oryzae), exhibited the highest dispersal efficacy in vitro. Two GHs, α-amylase (source: Bacillus sp.) and cellulase (source: A. niger), used in conjunction with meropenem demonstrated infection clearing ability in a mouse wound model. GHs were also effective in improving antibiotic clearance in diabetic mice. To examine their safety, we screened the GHs for toxicity in cell culture. Overall, there was an inverse relationship between enzyme exposure time and cellular toxicity, with twelve out of sixteen GHs demonstrating some level of toxicity in cell culture. However, only one GH exhibited harmful effects in mice. These results further support the ability of GHs to improve antibiotic clearance of biofilm-associated infections and help lay a foundation for establishing GHs as therapeutic agents for chronic wound infections.Whitni K. RedmanGarrett S. WelchAvery C. WilliamsAddyson J. DamronWillem O. NorthcutKendra P. RumbaughElsevierarticleBiofilmWound infectionGlycoside hydrolasesAntibiofilm agentDispersalBiotechnologyTP248.13-248.65MicrobiologyQR1-502ENBiofilm, Vol 3, Iss , Pp 100061- (2021)
institution DOAJ
collection DOAJ
language EN
topic Biofilm
Wound infection
Glycoside hydrolases
Antibiofilm agent
Dispersal
Biotechnology
TP248.13-248.65
Microbiology
QR1-502
spellingShingle Biofilm
Wound infection
Glycoside hydrolases
Antibiofilm agent
Dispersal
Biotechnology
TP248.13-248.65
Microbiology
QR1-502
Whitni K. Redman
Garrett S. Welch
Avery C. Williams
Addyson J. Damron
Willem O. Northcut
Kendra P. Rumbaugh
Efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds
description Novel anti-biofilm and dispersal agents are currently being investigated in an attempt to combat biofilm-associated wound infections. Glycoside hydrolases (GHs) are enzymes that hydrolyze the glycosidic bonds between sugars, such as those found within the exopolysaccharides of the biofilm matrix. Previous studies have shown that GHs can weaken the matrix, inducing bacterial dispersal, and improving antibiotic clearance. Yet, the number of GH enzymes that have been examined for potential therapeutic effects is limited. In this study, we screened sixteen GHs for their ability to disperse mono-microbial and polymicrobial biofilms grown in different environments. Six GHs, α-amylase (source: A. oryzae), alginate lyase (source: various algae), pectinase (source: Rhizopus sp.), amyloglucosidase (source: A. niger), inulinase (source: A. niger), and xylanase (source: A. oryzae), exhibited the highest dispersal efficacy in vitro. Two GHs, α-amylase (source: Bacillus sp.) and cellulase (source: A. niger), used in conjunction with meropenem demonstrated infection clearing ability in a mouse wound model. GHs were also effective in improving antibiotic clearance in diabetic mice. To examine their safety, we screened the GHs for toxicity in cell culture. Overall, there was an inverse relationship between enzyme exposure time and cellular toxicity, with twelve out of sixteen GHs demonstrating some level of toxicity in cell culture. However, only one GH exhibited harmful effects in mice. These results further support the ability of GHs to improve antibiotic clearance of biofilm-associated infections and help lay a foundation for establishing GHs as therapeutic agents for chronic wound infections.
format article
author Whitni K. Redman
Garrett S. Welch
Avery C. Williams
Addyson J. Damron
Willem O. Northcut
Kendra P. Rumbaugh
author_facet Whitni K. Redman
Garrett S. Welch
Avery C. Williams
Addyson J. Damron
Willem O. Northcut
Kendra P. Rumbaugh
author_sort Whitni K. Redman
title Efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds
title_short Efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds
title_full Efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds
title_fullStr Efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds
title_full_unstemmed Efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds
title_sort efficacy and safety of biofilm dispersal by glycoside hydrolases in wounds
publisher Elsevier
publishDate 2021
url https://doaj.org/article/00006f095d0046cabafe5a1f55b5ab54
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AT averycwilliams efficacyandsafetyofbiofilmdispersalbyglycosidehydrolasesinwounds
AT addysonjdamron efficacyandsafetyofbiofilmdispersalbyglycosidehydrolasesinwounds
AT willemonorthcut efficacyandsafetyofbiofilmdispersalbyglycosidehydrolasesinwounds
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