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Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation
Pseudomonas aeruginosa move across surfaces by using multiple Type IV Pili (TFP), motorized appendages capable of force generation via linear extension/retraction cycles, to generate surface motions collectively known as twitching motility. Pseudomonas cells arrive at a surface with low levels of pi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385500/ https://www.ncbi.nlm.nih.gov/pubmed/28393835 http://dx.doi.org/10.1038/srep45467 |
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author | Brill-Karniely, Yifat Jin, Fan Wong, Gerard C. L. Frenkel, Daan Dobnikar, Jure |
author_facet | Brill-Karniely, Yifat Jin, Fan Wong, Gerard C. L. Frenkel, Daan Dobnikar, Jure |
author_sort | Brill-Karniely, Yifat |
collection | PubMed |
description | Pseudomonas aeruginosa move across surfaces by using multiple Type IV Pili (TFP), motorized appendages capable of force generation via linear extension/retraction cycles, to generate surface motions collectively known as twitching motility. Pseudomonas cells arrive at a surface with low levels of piliation and TFP activity, which both progressively increase as the cells sense the presence of a surface. At present, it is not clear how twitching motility emerges from these initial minimal conditions. Here, we build a simple model for TFP-driven surface motility without complications from viscous and solid friction on surfaces. We discover the unanticipated structural requirement that TFP motors need to have a minimal amount of effective angular rigidity in order for cells to perform the various classes of experimentally-observed motions. Moreover, a surprisingly small number of TFP are needed to recapitulate movement signatures associated with twitching: Two TFP can already produce movements reminiscent of recently observed slingshot type motion. Interestingly, jerky slingshot motions characteristic of twitching motility comprise the transition region between different types of observed crawling behavior in the dynamical phase diagram, such as self-trapped localized motion, 2-D diffusive exploration, and super-diffusive persistent motion. |
format | Online Article Text |
id | pubmed-5385500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53855002017-04-12 Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation Brill-Karniely, Yifat Jin, Fan Wong, Gerard C. L. Frenkel, Daan Dobnikar, Jure Sci Rep Article Pseudomonas aeruginosa move across surfaces by using multiple Type IV Pili (TFP), motorized appendages capable of force generation via linear extension/retraction cycles, to generate surface motions collectively known as twitching motility. Pseudomonas cells arrive at a surface with low levels of piliation and TFP activity, which both progressively increase as the cells sense the presence of a surface. At present, it is not clear how twitching motility emerges from these initial minimal conditions. Here, we build a simple model for TFP-driven surface motility without complications from viscous and solid friction on surfaces. We discover the unanticipated structural requirement that TFP motors need to have a minimal amount of effective angular rigidity in order for cells to perform the various classes of experimentally-observed motions. Moreover, a surprisingly small number of TFP are needed to recapitulate movement signatures associated with twitching: Two TFP can already produce movements reminiscent of recently observed slingshot type motion. Interestingly, jerky slingshot motions characteristic of twitching motility comprise the transition region between different types of observed crawling behavior in the dynamical phase diagram, such as self-trapped localized motion, 2-D diffusive exploration, and super-diffusive persistent motion. Nature Publishing Group 2017-04-10 /pmc/articles/PMC5385500/ /pubmed/28393835 http://dx.doi.org/10.1038/srep45467 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Brill-Karniely, Yifat Jin, Fan Wong, Gerard C. L. Frenkel, Daan Dobnikar, Jure Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation |
title | Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation |
title_full | Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation |
title_fullStr | Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation |
title_full_unstemmed | Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation |
title_short | Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation |
title_sort | emergence of complex behavior in pili-based motility in early stages of p. aeruginosa surface adaptation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385500/ https://www.ncbi.nlm.nih.gov/pubmed/28393835 http://dx.doi.org/10.1038/srep45467 |
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