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Cell shape controls rheotaxis in small parasitic bacteria

Mycoplasmas, a group of small parasitic bacteria, adhere to and move across host cell surfaces. The role of motility across host cell surfaces in pathogenesis remains unclear. Here, we used optical microscopy to visualize rheotactic behavior in three phylogenetically distant species of Mycoplasma us...

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Detalles Bibliográficos
Autores principales: Nakane, Daisuke, Kabata, Yoshiki, Nishizaka, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282661/
https://www.ncbi.nlm.nih.gov/pubmed/35834494
http://dx.doi.org/10.1371/journal.ppat.1010648
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author Nakane, Daisuke
Kabata, Yoshiki
Nishizaka, Takayuki
author_facet Nakane, Daisuke
Kabata, Yoshiki
Nishizaka, Takayuki
author_sort Nakane, Daisuke
collection PubMed
description Mycoplasmas, a group of small parasitic bacteria, adhere to and move across host cell surfaces. The role of motility across host cell surfaces in pathogenesis remains unclear. Here, we used optical microscopy to visualize rheotactic behavior in three phylogenetically distant species of Mycoplasma using a microfluidic chamber that enabled the application of precisely controlled fluid flow. We show that directional movements against fluid flow occur synchronously with the polarized cell orienting itself to be parallel against the direction of flow. Analysis of depolarized cells revealed that morphology itself functions as a sensor to recognize rheological properties that mimic those found on host-cell surfaces. These results demonstrate the vital role of cell morphology and motility in responding to mechanical forces encountered in the native environment.
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spelling pubmed-92826612022-07-15 Cell shape controls rheotaxis in small parasitic bacteria Nakane, Daisuke Kabata, Yoshiki Nishizaka, Takayuki PLoS Pathog Research Article Mycoplasmas, a group of small parasitic bacteria, adhere to and move across host cell surfaces. The role of motility across host cell surfaces in pathogenesis remains unclear. Here, we used optical microscopy to visualize rheotactic behavior in three phylogenetically distant species of Mycoplasma using a microfluidic chamber that enabled the application of precisely controlled fluid flow. We show that directional movements against fluid flow occur synchronously with the polarized cell orienting itself to be parallel against the direction of flow. Analysis of depolarized cells revealed that morphology itself functions as a sensor to recognize rheological properties that mimic those found on host-cell surfaces. These results demonstrate the vital role of cell morphology and motility in responding to mechanical forces encountered in the native environment. Public Library of Science 2022-07-14 /pmc/articles/PMC9282661/ /pubmed/35834494 http://dx.doi.org/10.1371/journal.ppat.1010648 Text en © 2022 Nakane et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nakane, Daisuke
Kabata, Yoshiki
Nishizaka, Takayuki
Cell shape controls rheotaxis in small parasitic bacteria
title Cell shape controls rheotaxis in small parasitic bacteria
title_full Cell shape controls rheotaxis in small parasitic bacteria
title_fullStr Cell shape controls rheotaxis in small parasitic bacteria
title_full_unstemmed Cell shape controls rheotaxis in small parasitic bacteria
title_short Cell shape controls rheotaxis in small parasitic bacteria
title_sort cell shape controls rheotaxis in small parasitic bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282661/
https://www.ncbi.nlm.nih.gov/pubmed/35834494
http://dx.doi.org/10.1371/journal.ppat.1010648
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