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Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion
Hundreds of thousands of human implant procedures require surgical revision each year due to infection. Infections are difficult to treat with conventional antibiotics due to the formation of biofilm on the implant surface. We have developed a noninvasive method to eliminate biofilm on metal implant...
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/PMC8360946/ https://www.ncbi.nlm.nih.gov/pubmed/34385452 http://dx.doi.org/10.1038/s41522-021-00239-y |
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author | Wang, Qi Vachon, Jonathan Prasad, Bibin Pybus, Christine A. Lapin, Norman Chopra, Rajiv Greenberg, David E. |
author_facet | Wang, Qi Vachon, Jonathan Prasad, Bibin Pybus, Christine A. Lapin, Norman Chopra, Rajiv Greenberg, David E. |
author_sort | Wang, Qi |
collection | PubMed |
description | Hundreds of thousands of human implant procedures require surgical revision each year due to infection. Infections are difficult to treat with conventional antibiotics due to the formation of biofilm on the implant surface. We have developed a noninvasive method to eliminate biofilm on metal implants using heat generated by intermittent alternating magnetic fields (iAMF). Here, we demonstrate that heat and antibiotics are synergistic in biofilm elimination. For Pseudomonas aeruginosa biofilm, bacterial burden was reduced >3 log with iAMF and ciprofloxacin after 24 h compared with either treatment alone (p < 0.0001). This effect was not limited by pathogen or antibiotic as similar biofilm reductions were seen with iAMF and either linezolid or ceftriaxone in Staphylococcus aureus. iAMF and antibiotic efficacy was seen across various iAMF settings, including different iAMF target temperatures, dose durations, and dosing intervals. Initial mechanistic studies revealed membrane disruption as one factor important for AMF enhanced antibacterial activity in the biofilm setting. This study demonstrates the potential of utilizing a noninvasive approach to reduce biofilm off of metallic implants. |
format | Online Article Text |
id | pubmed-8360946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83609462021-08-19 Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion Wang, Qi Vachon, Jonathan Prasad, Bibin Pybus, Christine A. Lapin, Norman Chopra, Rajiv Greenberg, David E. NPJ Biofilms Microbiomes Article Hundreds of thousands of human implant procedures require surgical revision each year due to infection. Infections are difficult to treat with conventional antibiotics due to the formation of biofilm on the implant surface. We have developed a noninvasive method to eliminate biofilm on metal implants using heat generated by intermittent alternating magnetic fields (iAMF). Here, we demonstrate that heat and antibiotics are synergistic in biofilm elimination. For Pseudomonas aeruginosa biofilm, bacterial burden was reduced >3 log with iAMF and ciprofloxacin after 24 h compared with either treatment alone (p < 0.0001). This effect was not limited by pathogen or antibiotic as similar biofilm reductions were seen with iAMF and either linezolid or ceftriaxone in Staphylococcus aureus. iAMF and antibiotic efficacy was seen across various iAMF settings, including different iAMF target temperatures, dose durations, and dosing intervals. Initial mechanistic studies revealed membrane disruption as one factor important for AMF enhanced antibacterial activity in the biofilm setting. This study demonstrates the potential of utilizing a noninvasive approach to reduce biofilm off of metallic implants. Nature Publishing Group UK 2021-08-12 /pmc/articles/PMC8360946/ /pubmed/34385452 http://dx.doi.org/10.1038/s41522-021-00239-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Qi Vachon, Jonathan Prasad, Bibin Pybus, Christine A. Lapin, Norman Chopra, Rajiv Greenberg, David E. Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion |
title | Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion |
title_full | Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion |
title_fullStr | Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion |
title_full_unstemmed | Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion |
title_short | Alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion |
title_sort | alternating magnetic fields and antibiotics eradicate biofilm on metal in a synergistic fashion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360946/ https://www.ncbi.nlm.nih.gov/pubmed/34385452 http://dx.doi.org/10.1038/s41522-021-00239-y |
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