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Targeting microbial biofilms using Ficin, a nonspecific plant protease

Biofilms, the communities of surface-attached bacteria embedded into extracellular matrix, are ubiquitous microbial consortia securing the effective resistance of constituent cells to environmental impacts and host immune responses. Biofilm-embedded bacteria are generally inaccessible for antimicrob...

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Autores principales: Baidamshina, Diana R., Trizna, Elena Y., Holyavka, Marina G., Bogachev, Mikhail I., Artyukhov, Valeriy G., Akhatova, Farida S., Rozhina, Elvira V., Fakhrullin, Rawil F., Kayumov, Airat R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384253/
https://www.ncbi.nlm.nih.gov/pubmed/28387349
http://dx.doi.org/10.1038/srep46068
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author Baidamshina, Diana R.
Trizna, Elena Y.
Holyavka, Marina G.
Bogachev, Mikhail I.
Artyukhov, Valeriy G.
Akhatova, Farida S.
Rozhina, Elvira V.
Fakhrullin, Rawil F.
Kayumov, Airat R.
author_facet Baidamshina, Diana R.
Trizna, Elena Y.
Holyavka, Marina G.
Bogachev, Mikhail I.
Artyukhov, Valeriy G.
Akhatova, Farida S.
Rozhina, Elvira V.
Fakhrullin, Rawil F.
Kayumov, Airat R.
author_sort Baidamshina, Diana R.
collection PubMed
description Biofilms, the communities of surface-attached bacteria embedded into extracellular matrix, are ubiquitous microbial consortia securing the effective resistance of constituent cells to environmental impacts and host immune responses. Biofilm-embedded bacteria are generally inaccessible for antimicrobials, therefore the disruption of biofilm matrix is the potent approach to eradicate microbial biofilms. We demonstrate here the destruction of Staphylococcus aureus and Staphylococcus epidermidis biofilms with Ficin, a nonspecific plant protease. The biofilm thickness decreased two-fold after 24 hours treatment with Ficin at 10 μg/ml and six-fold at 1000 μg/ml concentration. We confirmed the successful destruction of biofilm structures and the significant decrease of non-specific bacterial adhesion to the surfaces after Ficin treatment using confocal laser scanning and atomic force microscopy. Importantly, Ficin treatment enhanced the effects of antibiotics on biofilms-embedded cells via disruption of biofilm matrices. Pre-treatment with Ficin (1000 μg/ml) considerably reduced the concentrations of ciprofloxacin and bezalkonium chloride required to suppress the viable Staphylococci by 3 orders of magnitude. We also demonstrated that Ficin is not cytotoxic towards human breast adenocarcinoma cells (MCF7) and dog adipose derived stem cells. Overall, Ficin is a potent tool for staphylococcal biofilm treatment and fabrication of novel antimicrobial therapeutics for medical and veterinary applications.
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spelling pubmed-53842532017-04-11 Targeting microbial biofilms using Ficin, a nonspecific plant protease Baidamshina, Diana R. Trizna, Elena Y. Holyavka, Marina G. Bogachev, Mikhail I. Artyukhov, Valeriy G. Akhatova, Farida S. Rozhina, Elvira V. Fakhrullin, Rawil F. Kayumov, Airat R. Sci Rep Article Biofilms, the communities of surface-attached bacteria embedded into extracellular matrix, are ubiquitous microbial consortia securing the effective resistance of constituent cells to environmental impacts and host immune responses. Biofilm-embedded bacteria are generally inaccessible for antimicrobials, therefore the disruption of biofilm matrix is the potent approach to eradicate microbial biofilms. We demonstrate here the destruction of Staphylococcus aureus and Staphylococcus epidermidis biofilms with Ficin, a nonspecific plant protease. The biofilm thickness decreased two-fold after 24 hours treatment with Ficin at 10 μg/ml and six-fold at 1000 μg/ml concentration. We confirmed the successful destruction of biofilm structures and the significant decrease of non-specific bacterial adhesion to the surfaces after Ficin treatment using confocal laser scanning and atomic force microscopy. Importantly, Ficin treatment enhanced the effects of antibiotics on biofilms-embedded cells via disruption of biofilm matrices. Pre-treatment with Ficin (1000 μg/ml) considerably reduced the concentrations of ciprofloxacin and bezalkonium chloride required to suppress the viable Staphylococci by 3 orders of magnitude. We also demonstrated that Ficin is not cytotoxic towards human breast adenocarcinoma cells (MCF7) and dog adipose derived stem cells. Overall, Ficin is a potent tool for staphylococcal biofilm treatment and fabrication of novel antimicrobial therapeutics for medical and veterinary applications. Nature Publishing Group 2017-04-07 /pmc/articles/PMC5384253/ /pubmed/28387349 http://dx.doi.org/10.1038/srep46068 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Baidamshina, Diana R.
Trizna, Elena Y.
Holyavka, Marina G.
Bogachev, Mikhail I.
Artyukhov, Valeriy G.
Akhatova, Farida S.
Rozhina, Elvira V.
Fakhrullin, Rawil F.
Kayumov, Airat R.
Targeting microbial biofilms using Ficin, a nonspecific plant protease
title Targeting microbial biofilms using Ficin, a nonspecific plant protease
title_full Targeting microbial biofilms using Ficin, a nonspecific plant protease
title_fullStr Targeting microbial biofilms using Ficin, a nonspecific plant protease
title_full_unstemmed Targeting microbial biofilms using Ficin, a nonspecific plant protease
title_short Targeting microbial biofilms using Ficin, a nonspecific plant protease
title_sort targeting microbial biofilms using ficin, a nonspecific plant protease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384253/
https://www.ncbi.nlm.nih.gov/pubmed/28387349
http://dx.doi.org/10.1038/srep46068
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