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Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei

Unicellular parasites have developed sophisticated swimming mechanisms to survive in a wide range of environments. Cell motility of African trypanosomes, parasites responsible for fatal illness in humans and animals, is crucial both in the insect vector and the mammalian host. Using millisecond-scal...

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Autores principales: Stellamanns, Eric, Uppaluri, Sravanti, Hochstetter, Axel, Heddergott, Niko, Engstler, Markus, Pfohl, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180810/
https://www.ncbi.nlm.nih.gov/pubmed/25269514
http://dx.doi.org/10.1038/srep06515
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author Stellamanns, Eric
Uppaluri, Sravanti
Hochstetter, Axel
Heddergott, Niko
Engstler, Markus
Pfohl, Thomas
author_facet Stellamanns, Eric
Uppaluri, Sravanti
Hochstetter, Axel
Heddergott, Niko
Engstler, Markus
Pfohl, Thomas
author_sort Stellamanns, Eric
collection PubMed
description Unicellular parasites have developed sophisticated swimming mechanisms to survive in a wide range of environments. Cell motility of African trypanosomes, parasites responsible for fatal illness in humans and animals, is crucial both in the insect vector and the mammalian host. Using millisecond-scale imaging in a microfluidics platform along with a custom made optical trap, we are able to confine single cells to study trypanosome motility. From the trapping characteristics of the cells, we determine the propulsion force generated by cells with a single flagellum as well as of dividing trypanosomes with two fully developed flagella. Estimates of the dissipative energy and the power generation of single cells obtained from the motility patterns of the trypanosomes within the optical trap indicate that specific motility characteristics, in addition to locomotion, may be required for antibody clearance. Introducing a steerable second optical trap we could further measure the force, which is generated at the flagellar tip. Differences in the cellular structure of the trypanosomes are correlated with the trapping and motility characteristics and in consequence with their propulsion force, dissipative energy and power generation.
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spelling pubmed-41808102014-10-02 Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei Stellamanns, Eric Uppaluri, Sravanti Hochstetter, Axel Heddergott, Niko Engstler, Markus Pfohl, Thomas Sci Rep Article Unicellular parasites have developed sophisticated swimming mechanisms to survive in a wide range of environments. Cell motility of African trypanosomes, parasites responsible for fatal illness in humans and animals, is crucial both in the insect vector and the mammalian host. Using millisecond-scale imaging in a microfluidics platform along with a custom made optical trap, we are able to confine single cells to study trypanosome motility. From the trapping characteristics of the cells, we determine the propulsion force generated by cells with a single flagellum as well as of dividing trypanosomes with two fully developed flagella. Estimates of the dissipative energy and the power generation of single cells obtained from the motility patterns of the trypanosomes within the optical trap indicate that specific motility characteristics, in addition to locomotion, may be required for antibody clearance. Introducing a steerable second optical trap we could further measure the force, which is generated at the flagellar tip. Differences in the cellular structure of the trypanosomes are correlated with the trapping and motility characteristics and in consequence with their propulsion force, dissipative energy and power generation. Nature Publishing Group 2014-10-01 /pmc/articles/PMC4180810/ /pubmed/25269514 http://dx.doi.org/10.1038/srep06515 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Stellamanns, Eric
Uppaluri, Sravanti
Hochstetter, Axel
Heddergott, Niko
Engstler, Markus
Pfohl, Thomas
Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei
title Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei
title_full Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei
title_fullStr Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei
title_full_unstemmed Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei
title_short Optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites Trypanosoma brucei brucei
title_sort optical trapping reveals propulsion forces, power generation and motility efficiency of the unicellular parasites trypanosoma brucei brucei
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180810/
https://www.ncbi.nlm.nih.gov/pubmed/25269514
http://dx.doi.org/10.1038/srep06515
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