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Developmental adaptations of trypanosome motility to the tsetse fly host environments unravel a multifaceted in vivo microswimmer system
The highly motile and versatile protozoan pathogen Trypanosoma brucei undergoes a complex life cycle in the tsetse fly. Here we introduce the host insect as an expedient model environment for microswimmer research, as it allows examination of microbial motion within a diversified, secluded and yet m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570225/ https://www.ncbi.nlm.nih.gov/pubmed/28807106 http://dx.doi.org/10.7554/eLife.27656 |
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author | Schuster, Sarah Krüger, Timothy Subota, Ines Thusek, Sina Rotureau, Brice Beilhack, Andreas Engstler, Markus |
author_facet | Schuster, Sarah Krüger, Timothy Subota, Ines Thusek, Sina Rotureau, Brice Beilhack, Andreas Engstler, Markus |
author_sort | Schuster, Sarah |
collection | PubMed |
description | The highly motile and versatile protozoan pathogen Trypanosoma brucei undergoes a complex life cycle in the tsetse fly. Here we introduce the host insect as an expedient model environment for microswimmer research, as it allows examination of microbial motion within a diversified, secluded and yet microscopically tractable space. During their week-long journey through the different microenvironments of the fly´s interior organs, the incessantly swimming trypanosomes cross various barriers and confined surroundings, with concurrently occurring major changes of parasite cell architecture. Multicolour light sheet fluorescence microscopy provided information about tsetse tissue topology with unprecedented resolution and allowed the first 3D analysis of the infection process. High-speed fluorescence microscopy illuminated the versatile behaviour of trypanosome developmental stages, ranging from solitary motion and near-wall swimming to collective motility in synchronised swarms and in confinement. We correlate the microenvironments and trypanosome morphologies to high-speed motility data, which paves the way for cross-disciplinary microswimmer research in a naturally evolved environment. DOI: http://dx.doi.org/10.7554/eLife.27656.001 |
format | Online Article Text |
id | pubmed-5570225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55702252017-08-28 Developmental adaptations of trypanosome motility to the tsetse fly host environments unravel a multifaceted in vivo microswimmer system Schuster, Sarah Krüger, Timothy Subota, Ines Thusek, Sina Rotureau, Brice Beilhack, Andreas Engstler, Markus eLife Biophysics and Structural Biology The highly motile and versatile protozoan pathogen Trypanosoma brucei undergoes a complex life cycle in the tsetse fly. Here we introduce the host insect as an expedient model environment for microswimmer research, as it allows examination of microbial motion within a diversified, secluded and yet microscopically tractable space. During their week-long journey through the different microenvironments of the fly´s interior organs, the incessantly swimming trypanosomes cross various barriers and confined surroundings, with concurrently occurring major changes of parasite cell architecture. Multicolour light sheet fluorescence microscopy provided information about tsetse tissue topology with unprecedented resolution and allowed the first 3D analysis of the infection process. High-speed fluorescence microscopy illuminated the versatile behaviour of trypanosome developmental stages, ranging from solitary motion and near-wall swimming to collective motility in synchronised swarms and in confinement. We correlate the microenvironments and trypanosome morphologies to high-speed motility data, which paves the way for cross-disciplinary microswimmer research in a naturally evolved environment. DOI: http://dx.doi.org/10.7554/eLife.27656.001 eLife Sciences Publications, Ltd 2017-08-15 /pmc/articles/PMC5570225/ /pubmed/28807106 http://dx.doi.org/10.7554/eLife.27656 Text en © 2017, Schuster et al 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 | Biophysics and Structural Biology Schuster, Sarah Krüger, Timothy Subota, Ines Thusek, Sina Rotureau, Brice Beilhack, Andreas Engstler, Markus Developmental adaptations of trypanosome motility to the tsetse fly host environments unravel a multifaceted in vivo microswimmer system |
title | Developmental adaptations of trypanosome motility to the tsetse fly host
environments unravel a multifaceted in vivo microswimmer system |
title_full | Developmental adaptations of trypanosome motility to the tsetse fly host
environments unravel a multifaceted in vivo microswimmer system |
title_fullStr | Developmental adaptations of trypanosome motility to the tsetse fly host
environments unravel a multifaceted in vivo microswimmer system |
title_full_unstemmed | Developmental adaptations of trypanosome motility to the tsetse fly host
environments unravel a multifaceted in vivo microswimmer system |
title_short | Developmental adaptations of trypanosome motility to the tsetse fly host
environments unravel a multifaceted in vivo microswimmer system |
title_sort | developmental adaptations of trypanosome motility to the tsetse fly host
environments unravel a multifaceted in vivo microswimmer system |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570225/ https://www.ncbi.nlm.nih.gov/pubmed/28807106 http://dx.doi.org/10.7554/eLife.27656 |
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