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Microscale communication between bacterial pathogens and the host epithelium
Pathogenic bacteria have evolved a variety of highly selective adhesins allowing these microbes to engage specific surface determinants of their eukaryotic host cells. Receptor clustering induced by the multivalent microorganisms will not only anchor the bacteria to the tissue, but will inevitably t...
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/PMC8497271/ https://www.ncbi.nlm.nih.gov/pubmed/34588625 http://dx.doi.org/10.1038/s41435-021-00149-1 |
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author | Mix, Ann-Kathrin Goob, Griseldis Sontowski, Erik Hauck, Christof R. |
author_facet | Mix, Ann-Kathrin Goob, Griseldis Sontowski, Erik Hauck, Christof R. |
author_sort | Mix, Ann-Kathrin |
collection | PubMed |
description | Pathogenic bacteria have evolved a variety of highly selective adhesins allowing these microbes to engage specific surface determinants of their eukaryotic host cells. Receptor clustering induced by the multivalent microorganisms will not only anchor the bacteria to the tissue, but will inevitably trigger host cell signaling. It has become clear, that these bacteria-initiated signaling events can be seen as a form of localized communication with host epithelial cells. Such a microscale communication can have immediate consequences in the form of changes in host cell membrane morphology or cytoskeletal organization, but can also lead to transcriptional responses and medium- and long-term alterations in cellular physiology. In this review, we will discuss several examples of this form of microscale communication between bacterial pathogens and mammalian host cells and try to delineate their downstream ramifications in the infection process. Furthermore, we will highlight recent findings that specialized pathogenic bacteria utilize the adhesin-based interaction to diffuse the short-range messenger molecule nitric oxide into the host tissue. While anti-adhesive strategies to disrupt the initial bacterial attachment have not yet translated into medical applications, the ability to interfere with the microscale communication emanating on the host side provides an unconventional approach for preventing infectious diseases. |
format | Online Article Text |
id | pubmed-8497271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84972712021-10-19 Microscale communication between bacterial pathogens and the host epithelium Mix, Ann-Kathrin Goob, Griseldis Sontowski, Erik Hauck, Christof R. Genes Immun Review Article Pathogenic bacteria have evolved a variety of highly selective adhesins allowing these microbes to engage specific surface determinants of their eukaryotic host cells. Receptor clustering induced by the multivalent microorganisms will not only anchor the bacteria to the tissue, but will inevitably trigger host cell signaling. It has become clear, that these bacteria-initiated signaling events can be seen as a form of localized communication with host epithelial cells. Such a microscale communication can have immediate consequences in the form of changes in host cell membrane morphology or cytoskeletal organization, but can also lead to transcriptional responses and medium- and long-term alterations in cellular physiology. In this review, we will discuss several examples of this form of microscale communication between bacterial pathogens and mammalian host cells and try to delineate their downstream ramifications in the infection process. Furthermore, we will highlight recent findings that specialized pathogenic bacteria utilize the adhesin-based interaction to diffuse the short-range messenger molecule nitric oxide into the host tissue. While anti-adhesive strategies to disrupt the initial bacterial attachment have not yet translated into medical applications, the ability to interfere with the microscale communication emanating on the host side provides an unconventional approach for preventing infectious diseases. Nature Publishing Group UK 2021-09-29 2021 /pmc/articles/PMC8497271/ /pubmed/34588625 http://dx.doi.org/10.1038/s41435-021-00149-1 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 | Review Article Mix, Ann-Kathrin Goob, Griseldis Sontowski, Erik Hauck, Christof R. Microscale communication between bacterial pathogens and the host epithelium |
title | Microscale communication between bacterial pathogens and the host epithelium |
title_full | Microscale communication between bacterial pathogens and the host epithelium |
title_fullStr | Microscale communication between bacterial pathogens and the host epithelium |
title_full_unstemmed | Microscale communication between bacterial pathogens and the host epithelium |
title_short | Microscale communication between bacterial pathogens and the host epithelium |
title_sort | microscale communication between bacterial pathogens and the host epithelium |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497271/ https://www.ncbi.nlm.nih.gov/pubmed/34588625 http://dx.doi.org/10.1038/s41435-021-00149-1 |
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