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Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms
Staphylococcus aureus is commonly associated with biofilm-related infections and contributes to the large financial loss that accompany nosocomial infections. The micrococcal nuclease Nuc1 enzyme limits biofilm formation via cleavage of eDNA, a structural component of the biofilm matrix. Solid surfa...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374737/ https://www.ncbi.nlm.nih.gov/pubmed/32694559 http://dx.doi.org/10.1038/s41598-020-69084-x |
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author | Forson, Abigail M. van der Mei, Henny C. Sjollema, Jelmer |
author_facet | Forson, Abigail M. van der Mei, Henny C. Sjollema, Jelmer |
author_sort | Forson, Abigail M. |
collection | PubMed |
description | Staphylococcus aureus is commonly associated with biofilm-related infections and contributes to the large financial loss that accompany nosocomial infections. The micrococcal nuclease Nuc1 enzyme limits biofilm formation via cleavage of eDNA, a structural component of the biofilm matrix. Solid surface hydrophobicity influences bacterial adhesion forces and may as well influence eDNA production. Therefore, it is hypothesized that the impact of Nuc1 activity is dependent on surface characteristics of solid surfaces. For this reason, this study investigated the influence of solid surface hydrophobicity on S. aureus Newman biofilms where Nuc1 is constitutively produced. To this end, biofilms of both a wild-type and a nuc1 knockout mutant strain, grown on glass, salinized glass and Pluronic F-127-coated silanized glass were analysed. Results indicated that biofilms can grow in the presence of Nuc1 activity. Also, Nuc1 and solid surface hydrophobicity significantly affected the biofilm 3D-architecture. In particular, biofilm densities of the wild-type strain on hydrophilic surfaces appeared higher than of the mutant nuc1 knockout strain. Since virulence is related to bacterial cell densities, this suggests that the virulence of S. aureus Newman biofilms is increased by its nuclease production in particular on a hydrophilic surface. |
format | Online Article Text |
id | pubmed-7374737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73747372020-07-22 Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms Forson, Abigail M. van der Mei, Henny C. Sjollema, Jelmer Sci Rep Article Staphylococcus aureus is commonly associated with biofilm-related infections and contributes to the large financial loss that accompany nosocomial infections. The micrococcal nuclease Nuc1 enzyme limits biofilm formation via cleavage of eDNA, a structural component of the biofilm matrix. Solid surface hydrophobicity influences bacterial adhesion forces and may as well influence eDNA production. Therefore, it is hypothesized that the impact of Nuc1 activity is dependent on surface characteristics of solid surfaces. For this reason, this study investigated the influence of solid surface hydrophobicity on S. aureus Newman biofilms where Nuc1 is constitutively produced. To this end, biofilms of both a wild-type and a nuc1 knockout mutant strain, grown on glass, salinized glass and Pluronic F-127-coated silanized glass were analysed. Results indicated that biofilms can grow in the presence of Nuc1 activity. Also, Nuc1 and solid surface hydrophobicity significantly affected the biofilm 3D-architecture. In particular, biofilm densities of the wild-type strain on hydrophilic surfaces appeared higher than of the mutant nuc1 knockout strain. Since virulence is related to bacterial cell densities, this suggests that the virulence of S. aureus Newman biofilms is increased by its nuclease production in particular on a hydrophilic surface. Nature Publishing Group UK 2020-07-21 /pmc/articles/PMC7374737/ /pubmed/32694559 http://dx.doi.org/10.1038/s41598-020-69084-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Forson, Abigail M. van der Mei, Henny C. Sjollema, Jelmer Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms |
title | Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms |
title_full | Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms |
title_fullStr | Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms |
title_full_unstemmed | Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms |
title_short | Impact of solid surface hydrophobicity and micrococcal nuclease production on Staphylococcus aureus Newman biofilms |
title_sort | impact of solid surface hydrophobicity and micrococcal nuclease production on staphylococcus aureus newman biofilms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374737/ https://www.ncbi.nlm.nih.gov/pubmed/32694559 http://dx.doi.org/10.1038/s41598-020-69084-x |
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