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Insights into flagellar function and mechanism from the squid–vibrio symbiosis
Flagella are essential and multifunctional nanomachines that not only move symbionts towards their tissue colonization site, but also play multiple roles in communicating with the host. Thus, untangling the activities of flagella in reaching, interacting, and signaling the host, as well as in biofil...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814793/ https://www.ncbi.nlm.nih.gov/pubmed/31666982 http://dx.doi.org/10.1038/s41522-019-0106-5 |
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author | Aschtgen, Marie-Stephanie Brennan, Caitlin A. Nikolakakis, Kiel Cohen, Stephanie McFall-Ngai, Margaret Ruby, Edward G. |
author_facet | Aschtgen, Marie-Stephanie Brennan, Caitlin A. Nikolakakis, Kiel Cohen, Stephanie McFall-Ngai, Margaret Ruby, Edward G. |
author_sort | Aschtgen, Marie-Stephanie |
collection | PubMed |
description | Flagella are essential and multifunctional nanomachines that not only move symbionts towards their tissue colonization site, but also play multiple roles in communicating with the host. Thus, untangling the activities of flagella in reaching, interacting, and signaling the host, as well as in biofilm formation and the establishment of a persistent colonization, is a complex problem. The squid–vibrio system offers a unique model to study the many ways that bacterial flagella can influence a beneficial association and, generally, other bacteria–host interactions. Vibrio fischeri is a bioluminescent bacterium that colonizes the Hawaiian bobtail squid, Euprymna scolopes. Over the last 15 years, the structure, assembly, and functions of V. fischeri flagella, including not only motility and chemotaxis, but also biofilm formation and symbiotic signaling, have been revealed. Here we discuss these discoveries in the perspective of other host–bacteria interactions. |
format | Online Article Text |
id | pubmed-6814793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68147932019-10-30 Insights into flagellar function and mechanism from the squid–vibrio symbiosis Aschtgen, Marie-Stephanie Brennan, Caitlin A. Nikolakakis, Kiel Cohen, Stephanie McFall-Ngai, Margaret Ruby, Edward G. NPJ Biofilms Microbiomes Review Article Flagella are essential and multifunctional nanomachines that not only move symbionts towards their tissue colonization site, but also play multiple roles in communicating with the host. Thus, untangling the activities of flagella in reaching, interacting, and signaling the host, as well as in biofilm formation and the establishment of a persistent colonization, is a complex problem. The squid–vibrio system offers a unique model to study the many ways that bacterial flagella can influence a beneficial association and, generally, other bacteria–host interactions. Vibrio fischeri is a bioluminescent bacterium that colonizes the Hawaiian bobtail squid, Euprymna scolopes. Over the last 15 years, the structure, assembly, and functions of V. fischeri flagella, including not only motility and chemotaxis, but also biofilm formation and symbiotic signaling, have been revealed. Here we discuss these discoveries in the perspective of other host–bacteria interactions. Nature Publishing Group UK 2019-10-25 /pmc/articles/PMC6814793/ /pubmed/31666982 http://dx.doi.org/10.1038/s41522-019-0106-5 Text en © The Author(s) 2019 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 | Review Article Aschtgen, Marie-Stephanie Brennan, Caitlin A. Nikolakakis, Kiel Cohen, Stephanie McFall-Ngai, Margaret Ruby, Edward G. Insights into flagellar function and mechanism from the squid–vibrio symbiosis |
title | Insights into flagellar function and mechanism from the squid–vibrio symbiosis |
title_full | Insights into flagellar function and mechanism from the squid–vibrio symbiosis |
title_fullStr | Insights into flagellar function and mechanism from the squid–vibrio symbiosis |
title_full_unstemmed | Insights into flagellar function and mechanism from the squid–vibrio symbiosis |
title_short | Insights into flagellar function and mechanism from the squid–vibrio symbiosis |
title_sort | insights into flagellar function and mechanism from the squid–vibrio symbiosis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814793/ https://www.ncbi.nlm.nih.gov/pubmed/31666982 http://dx.doi.org/10.1038/s41522-019-0106-5 |
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