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Human organoid biofilm model for assessing antibiofilm activity of novel agents
Bacterial biofilms cause 65% of all human infections and are highly resistant to antibiotic therapy but lack specific treatments. To provide a human organoid model for studying host-microbe interplay and enabling screening for novel antibiofilm agents, a human epidermis organoid model with robust me...
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/PMC7835231/ https://www.ncbi.nlm.nih.gov/pubmed/33495449 http://dx.doi.org/10.1038/s41522-020-00182-4 |
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author | Wu, Bing (Catherine) Haney, Evan F. Akhoundsadegh, Noushin Pletzer, Daniel Trimble, Michael J. Adriaans, Alwin E. Nibbering, Peter H. Hancock, Robert E. W. |
author_facet | Wu, Bing (Catherine) Haney, Evan F. Akhoundsadegh, Noushin Pletzer, Daniel Trimble, Michael J. Adriaans, Alwin E. Nibbering, Peter H. Hancock, Robert E. W. |
author_sort | Wu, Bing (Catherine) |
collection | PubMed |
description | Bacterial biofilms cause 65% of all human infections and are highly resistant to antibiotic therapy but lack specific treatments. To provide a human organoid model for studying host-microbe interplay and enabling screening for novel antibiofilm agents, a human epidermis organoid model with robust methicillin-resistant Staphylococcus aureus (MRSA) USA300 and Pseudomonas aeruginosa PAO1 biofilm was developed. Treatment of 1-day and 3-day MRSA and PAO1 biofilms with antibiofilm peptide DJK-5 significantly and substantially reduced the bacterial burden. This model enabled the screening of synthetic host defense peptides, revealing their superior antibiofilm activity against MRSA compared to the antibiotic mupirocin. The model was extended to evaluate thermally wounded skin infected with MRSA biofilms resulting in increased bacterial load, cytotoxicity, and pro-inflammatory cytokine levels that were all reduced upon treatment with DJK-5. Combination treatment of DJK-5 with an anti-inflammatory peptide, 1002, further reduced cytotoxicity and skin inflammation. |
format | Online Article Text |
id | pubmed-7835231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78352312021-01-29 Human organoid biofilm model for assessing antibiofilm activity of novel agents Wu, Bing (Catherine) Haney, Evan F. Akhoundsadegh, Noushin Pletzer, Daniel Trimble, Michael J. Adriaans, Alwin E. Nibbering, Peter H. Hancock, Robert E. W. NPJ Biofilms Microbiomes Article Bacterial biofilms cause 65% of all human infections and are highly resistant to antibiotic therapy but lack specific treatments. To provide a human organoid model for studying host-microbe interplay and enabling screening for novel antibiofilm agents, a human epidermis organoid model with robust methicillin-resistant Staphylococcus aureus (MRSA) USA300 and Pseudomonas aeruginosa PAO1 biofilm was developed. Treatment of 1-day and 3-day MRSA and PAO1 biofilms with antibiofilm peptide DJK-5 significantly and substantially reduced the bacterial burden. This model enabled the screening of synthetic host defense peptides, revealing their superior antibiofilm activity against MRSA compared to the antibiotic mupirocin. The model was extended to evaluate thermally wounded skin infected with MRSA biofilms resulting in increased bacterial load, cytotoxicity, and pro-inflammatory cytokine levels that were all reduced upon treatment with DJK-5. Combination treatment of DJK-5 with an anti-inflammatory peptide, 1002, further reduced cytotoxicity and skin inflammation. Nature Publishing Group UK 2021-01-25 /pmc/articles/PMC7835231/ /pubmed/33495449 http://dx.doi.org/10.1038/s41522-020-00182-4 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 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 Wu, Bing (Catherine) Haney, Evan F. Akhoundsadegh, Noushin Pletzer, Daniel Trimble, Michael J. Adriaans, Alwin E. Nibbering, Peter H. Hancock, Robert E. W. Human organoid biofilm model for assessing antibiofilm activity of novel agents |
title | Human organoid biofilm model for assessing antibiofilm activity of novel agents |
title_full | Human organoid biofilm model for assessing antibiofilm activity of novel agents |
title_fullStr | Human organoid biofilm model for assessing antibiofilm activity of novel agents |
title_full_unstemmed | Human organoid biofilm model for assessing antibiofilm activity of novel agents |
title_short | Human organoid biofilm model for assessing antibiofilm activity of novel agents |
title_sort | human organoid biofilm model for assessing antibiofilm activity of novel agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835231/ https://www.ncbi.nlm.nih.gov/pubmed/33495449 http://dx.doi.org/10.1038/s41522-020-00182-4 |
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