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Transient locking of the hook procures enhanced motility to flagellated bacteria
Flagellated bacteria often proliferate in inhomogeneous environments, such as biofilms, swarms and soil. In such media, bacteria are observed to move efficiently only if they can get out of “dead ends” by changing drastically their swimming direction, and even to completely reverse it. Even though t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703839/ https://www.ncbi.nlm.nih.gov/pubmed/29180634 http://dx.doi.org/10.1038/s41598-017-16562-4 |
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author | Duchesne, Ismaël Galstian, Tigran Rainville, Simon |
author_facet | Duchesne, Ismaël Galstian, Tigran Rainville, Simon |
author_sort | Duchesne, Ismaël |
collection | PubMed |
description | Flagellated bacteria often proliferate in inhomogeneous environments, such as biofilms, swarms and soil. In such media, bacteria are observed to move efficiently only if they can get out of “dead ends” by changing drastically their swimming direction, and even to completely reverse it. Even though these reorientations are ubiquitous, we have only recently begun to describe and understand how they happen. In the present work, we visualized the flagella of bacteria swimming in a soft agar solution. The surprising observation that the filaments do not rotate while being flipped from one side of the cell to the other suggests that reversals are driven directly by the motor rather than by the thrust created by the rotating filament. This was confirmed by observing bacteria in a liquid crystal, where the linear movement of bacteria greatly simplifies the analysis. These observations suggest that the reversal and reorientation processes involve a temporary locking of the flagellum’s hook, which is the normally flexible joint between the rotary motor and the long helical filament that propels the cell. This newly described locked-hook mode occurs only when the motor switches to a clockwise rotation. That correlates with other phenomena that are triggered by a switch in one direction and not the other. |
format | Online Article Text |
id | pubmed-5703839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57038392017-11-30 Transient locking of the hook procures enhanced motility to flagellated bacteria Duchesne, Ismaël Galstian, Tigran Rainville, Simon Sci Rep Article Flagellated bacteria often proliferate in inhomogeneous environments, such as biofilms, swarms and soil. In such media, bacteria are observed to move efficiently only if they can get out of “dead ends” by changing drastically their swimming direction, and even to completely reverse it. Even though these reorientations are ubiquitous, we have only recently begun to describe and understand how they happen. In the present work, we visualized the flagella of bacteria swimming in a soft agar solution. The surprising observation that the filaments do not rotate while being flipped from one side of the cell to the other suggests that reversals are driven directly by the motor rather than by the thrust created by the rotating filament. This was confirmed by observing bacteria in a liquid crystal, where the linear movement of bacteria greatly simplifies the analysis. These observations suggest that the reversal and reorientation processes involve a temporary locking of the flagellum’s hook, which is the normally flexible joint between the rotary motor and the long helical filament that propels the cell. This newly described locked-hook mode occurs only when the motor switches to a clockwise rotation. That correlates with other phenomena that are triggered by a switch in one direction and not the other. Nature Publishing Group UK 2017-11-27 /pmc/articles/PMC5703839/ /pubmed/29180634 http://dx.doi.org/10.1038/s41598-017-16562-4 Text en © The Author(s) 2017 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 Duchesne, Ismaël Galstian, Tigran Rainville, Simon Transient locking of the hook procures enhanced motility to flagellated bacteria |
title | Transient locking of the hook procures enhanced motility to flagellated bacteria |
title_full | Transient locking of the hook procures enhanced motility to flagellated bacteria |
title_fullStr | Transient locking of the hook procures enhanced motility to flagellated bacteria |
title_full_unstemmed | Transient locking of the hook procures enhanced motility to flagellated bacteria |
title_short | Transient locking of the hook procures enhanced motility to flagellated bacteria |
title_sort | transient locking of the hook procures enhanced motility to flagellated bacteria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703839/ https://www.ncbi.nlm.nih.gov/pubmed/29180634 http://dx.doi.org/10.1038/s41598-017-16562-4 |
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