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Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus
The pathogen Staphylococcus aureus can readily develop antibiotic resistance and evade the human immune system, which is associated with reduced levels of neutrophil recruitment. Here, we present a class of antibacterial peptides with potential to act both as antibiotics and as neutrophil chemoattra...
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/PMC8546149/ https://www.ncbi.nlm.nih.gov/pubmed/34697316 http://dx.doi.org/10.1038/s41467-021-26244-5 |
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author | Payne, Jennifer A. E. Tailhades, Julien Ellett, Felix Kostoulias, Xenia Fulcher, Alex J. Fu, Ting Leung, Ryan Louch, Stephanie Tran, Amy Weber, Severin A. Schittenhelm, Ralf B. Lieschke, Graham J. Qin, Chengxue Helena Irima, Daniel Peleg, Anton Y. Cryle, Max J. |
author_facet | Payne, Jennifer A. E. Tailhades, Julien Ellett, Felix Kostoulias, Xenia Fulcher, Alex J. Fu, Ting Leung, Ryan Louch, Stephanie Tran, Amy Weber, Severin A. Schittenhelm, Ralf B. Lieschke, Graham J. Qin, Chengxue Helena Irima, Daniel Peleg, Anton Y. Cryle, Max J. |
author_sort | Payne, Jennifer A. E. |
collection | PubMed |
description | The pathogen Staphylococcus aureus can readily develop antibiotic resistance and evade the human immune system, which is associated with reduced levels of neutrophil recruitment. Here, we present a class of antibacterial peptides with potential to act both as antibiotics and as neutrophil chemoattractants. The compounds, which we term ‘antibiotic-chemoattractants’, consist of a formylated peptide (known to act as chemoattractant for neutrophil recruitment) that is covalently linked to the antibiotic vancomycin (known to bind to the bacterial cell wall). We use a combination of in vitro assays, cellular assays, infection-on-a-chip and in vivo mouse models to show that the compounds improve the recruitment, engulfment and killing of S. aureus by neutrophils. Furthermore, optimizing the formyl peptide sequence can enhance neutrophil activity through differential activation of formyl peptide receptors. Thus, we propose antibiotic-chemoattractants as an alternate approach for antibiotic development. |
format | Online Article Text |
id | pubmed-8546149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85461492021-10-29 Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus Payne, Jennifer A. E. Tailhades, Julien Ellett, Felix Kostoulias, Xenia Fulcher, Alex J. Fu, Ting Leung, Ryan Louch, Stephanie Tran, Amy Weber, Severin A. Schittenhelm, Ralf B. Lieschke, Graham J. Qin, Chengxue Helena Irima, Daniel Peleg, Anton Y. Cryle, Max J. Nat Commun Article The pathogen Staphylococcus aureus can readily develop antibiotic resistance and evade the human immune system, which is associated with reduced levels of neutrophil recruitment. Here, we present a class of antibacterial peptides with potential to act both as antibiotics and as neutrophil chemoattractants. The compounds, which we term ‘antibiotic-chemoattractants’, consist of a formylated peptide (known to act as chemoattractant for neutrophil recruitment) that is covalently linked to the antibiotic vancomycin (known to bind to the bacterial cell wall). We use a combination of in vitro assays, cellular assays, infection-on-a-chip and in vivo mouse models to show that the compounds improve the recruitment, engulfment and killing of S. aureus by neutrophils. Furthermore, optimizing the formyl peptide sequence can enhance neutrophil activity through differential activation of formyl peptide receptors. Thus, we propose antibiotic-chemoattractants as an alternate approach for antibiotic development. Nature Publishing Group UK 2021-10-25 /pmc/articles/PMC8546149/ /pubmed/34697316 http://dx.doi.org/10.1038/s41467-021-26244-5 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 Payne, Jennifer A. E. Tailhades, Julien Ellett, Felix Kostoulias, Xenia Fulcher, Alex J. Fu, Ting Leung, Ryan Louch, Stephanie Tran, Amy Weber, Severin A. Schittenhelm, Ralf B. Lieschke, Graham J. Qin, Chengxue Helena Irima, Daniel Peleg, Anton Y. Cryle, Max J. Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus |
title | Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus |
title_full | Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus |
title_fullStr | Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus |
title_full_unstemmed | Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus |
title_short | Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus |
title_sort | antibiotic-chemoattractants enhance neutrophil clearance of staphylococcus aureus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546149/ https://www.ncbi.nlm.nih.gov/pubmed/34697316 http://dx.doi.org/10.1038/s41467-021-26244-5 |
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