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Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate
In S. aureus biofilms, bacteria are embedded in a matrix of extracellular polymeric substances (EPS) and are highly tolerant to antimicrobial drugs. We thus sought to identify non-antibiotic substances with broad-spectrum activity able to destroy the EPS matrix and enhance the effect of antibiotics...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973569/ https://www.ncbi.nlm.nih.gov/pubmed/33737602 http://dx.doi.org/10.1038/s41598-021-85722-4 |
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author | Liu, JingJing Madec, Jean-Yves Bousquet-Mélou, Alain Haenni, Marisa Ferran, Aude A. |
author_facet | Liu, JingJing Madec, Jean-Yves Bousquet-Mélou, Alain Haenni, Marisa Ferran, Aude A. |
author_sort | Liu, JingJing |
collection | PubMed |
description | In S. aureus biofilms, bacteria are embedded in a matrix of extracellular polymeric substances (EPS) and are highly tolerant to antimicrobial drugs. We thus sought to identify non-antibiotic substances with broad-spectrum activity able to destroy the EPS matrix and enhance the effect of antibiotics on embedded biofilm bacteria. Among eight substances tested, subtilisin A (0.01 U/mL) and calcium gluconate (CaG, Ca(2+) 1.25 mmol/L) significantly reduced the biomass of biofilms formed by at least 21/24 S. aureus isolates. Confocal laser scanning microscopy confirmed that they both eliminated nearly all the proteins and PNAG from the matrix. By contrast, antibiotics alone had nearly no effect on biofilm biomass and the selected one (oxytetracycline-OTC) could only slightly reduce biofilm bacteria. The combination of OTC with CaG or subtilisin A led to an additive reduction (average of 2 log(10) CFU/mL) of embedded biofilm bacteria on the isolates susceptible to OTC (MBC < 10 μg/mL, 11/24). Moreover, these two combinations led to a reduction of the embedded biofilm bacteria higher than 3 log(10) CFU/mL for 20–25% of the isolates. Further studies are now required to better understand the factors that cause the biofilm produced by specific isolates (20–25%) to be susceptible to the combinations. |
format | Online Article Text |
id | pubmed-7973569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79735692021-03-19 Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate Liu, JingJing Madec, Jean-Yves Bousquet-Mélou, Alain Haenni, Marisa Ferran, Aude A. Sci Rep Article In S. aureus biofilms, bacteria are embedded in a matrix of extracellular polymeric substances (EPS) and are highly tolerant to antimicrobial drugs. We thus sought to identify non-antibiotic substances with broad-spectrum activity able to destroy the EPS matrix and enhance the effect of antibiotics on embedded biofilm bacteria. Among eight substances tested, subtilisin A (0.01 U/mL) and calcium gluconate (CaG, Ca(2+) 1.25 mmol/L) significantly reduced the biomass of biofilms formed by at least 21/24 S. aureus isolates. Confocal laser scanning microscopy confirmed that they both eliminated nearly all the proteins and PNAG from the matrix. By contrast, antibiotics alone had nearly no effect on biofilm biomass and the selected one (oxytetracycline-OTC) could only slightly reduce biofilm bacteria. The combination of OTC with CaG or subtilisin A led to an additive reduction (average of 2 log(10) CFU/mL) of embedded biofilm bacteria on the isolates susceptible to OTC (MBC < 10 μg/mL, 11/24). Moreover, these two combinations led to a reduction of the embedded biofilm bacteria higher than 3 log(10) CFU/mL for 20–25% of the isolates. Further studies are now required to better understand the factors that cause the biofilm produced by specific isolates (20–25%) to be susceptible to the combinations. Nature Publishing Group UK 2021-03-18 /pmc/articles/PMC7973569/ /pubmed/33737602 http://dx.doi.org/10.1038/s41598-021-85722-4 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, JingJing Madec, Jean-Yves Bousquet-Mélou, Alain Haenni, Marisa Ferran, Aude A. Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate |
title | Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate |
title_full | Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate |
title_fullStr | Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate |
title_full_unstemmed | Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate |
title_short | Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate |
title_sort | destruction of staphylococcus aureus biofilms by combining an antibiotic with subtilisin a or calcium gluconate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973569/ https://www.ncbi.nlm.nih.gov/pubmed/33737602 http://dx.doi.org/10.1038/s41598-021-85722-4 |
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