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High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria
Bacteria propel and change direction by rotating long, helical filaments, called flagella. The number of flagella, their arrangement on the cell body and their sense of rotation hypothetically determine the locomotion characteristics of a species. The movement of the most rapid microorganisms has in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010408/ https://www.ncbi.nlm.nih.gov/pubmed/31989923 http://dx.doi.org/10.7554/eLife.47551 |
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author | Bente, Klaas Mohammadinejad, Sarah Charsooghi, Mohammad Avalin Bachmann, Felix Codutti, Agnese Lefèvre, Christopher T Klumpp, Stefan Faivre, Damien |
author_facet | Bente, Klaas Mohammadinejad, Sarah Charsooghi, Mohammad Avalin Bachmann, Felix Codutti, Agnese Lefèvre, Christopher T Klumpp, Stefan Faivre, Damien |
author_sort | Bente, Klaas |
collection | PubMed |
description | Bacteria propel and change direction by rotating long, helical filaments, called flagella. The number of flagella, their arrangement on the cell body and their sense of rotation hypothetically determine the locomotion characteristics of a species. The movement of the most rapid microorganisms has in particular remained unexplored because of additional experimental limitations. We show that magnetotactic cocci with two flagella bundles on one pole swim faster than 500 µm·s(−1) along a double helical path, making them one of the fastest natural microswimmers. We additionally reveal that the cells reorient in less than 5 ms, an order of magnitude faster than reported so far for any other bacteria. Using hydrodynamic modeling, we demonstrate that a mode where a pushing and a pulling bundle cooperate is the only possibility to enable both helical tracks and fast reorientations. The advantage of sheathed flagella bundles is the high rigidity, making high swimming speeds possible. |
format | Online Article Text |
id | pubmed-7010408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-70104082020-02-12 High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria Bente, Klaas Mohammadinejad, Sarah Charsooghi, Mohammad Avalin Bachmann, Felix Codutti, Agnese Lefèvre, Christopher T Klumpp, Stefan Faivre, Damien eLife Physics of Living Systems Bacteria propel and change direction by rotating long, helical filaments, called flagella. The number of flagella, their arrangement on the cell body and their sense of rotation hypothetically determine the locomotion characteristics of a species. The movement of the most rapid microorganisms has in particular remained unexplored because of additional experimental limitations. We show that magnetotactic cocci with two flagella bundles on one pole swim faster than 500 µm·s(−1) along a double helical path, making them one of the fastest natural microswimmers. We additionally reveal that the cells reorient in less than 5 ms, an order of magnitude faster than reported so far for any other bacteria. Using hydrodynamic modeling, we demonstrate that a mode where a pushing and a pulling bundle cooperate is the only possibility to enable both helical tracks and fast reorientations. The advantage of sheathed flagella bundles is the high rigidity, making high swimming speeds possible. eLife Sciences Publications, Ltd 2020-01-28 /pmc/articles/PMC7010408/ /pubmed/31989923 http://dx.doi.org/10.7554/eLife.47551 Text en © 2020, Bente et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Physics of Living Systems Bente, Klaas Mohammadinejad, Sarah Charsooghi, Mohammad Avalin Bachmann, Felix Codutti, Agnese Lefèvre, Christopher T Klumpp, Stefan Faivre, Damien High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria |
title | High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria |
title_full | High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria |
title_fullStr | High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria |
title_full_unstemmed | High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria |
title_short | High-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria |
title_sort | high-speed motility originates from cooperatively pushing and pulling flagella bundles in bilophotrichous bacteria |
topic | Physics of Living Systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010408/ https://www.ncbi.nlm.nih.gov/pubmed/31989923 http://dx.doi.org/10.7554/eLife.47551 |
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