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Flagellum couples cell shape to motility in Trypanosoma brucei
In the unicellular parasite Trypanosoma brucei, the causative agent of human African sleeping sickness, complex swimming behavior is driven by a flagellum laterally attached to the long and slender cell body. Using microfluidic assays, we demonstrated that T. brucei can penetrate through an orifice...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042131/ https://www.ncbi.nlm.nih.gov/pubmed/29891682 http://dx.doi.org/10.1073/pnas.1722618115 |
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author | Sun, Stella Y. Kaelber, Jason T. Chen, Muyuan Dong, Xiaoduo Nematbakhsh, Yasaman Shi, Jian Dougherty, Matthew Lim, Chwee Teck Schmid, Michael F. Chiu, Wah He, Cynthia Y. |
author_facet | Sun, Stella Y. Kaelber, Jason T. Chen, Muyuan Dong, Xiaoduo Nematbakhsh, Yasaman Shi, Jian Dougherty, Matthew Lim, Chwee Teck Schmid, Michael F. Chiu, Wah He, Cynthia Y. |
author_sort | Sun, Stella Y. |
collection | PubMed |
description | In the unicellular parasite Trypanosoma brucei, the causative agent of human African sleeping sickness, complex swimming behavior is driven by a flagellum laterally attached to the long and slender cell body. Using microfluidic assays, we demonstrated that T. brucei can penetrate through an orifice smaller than its maximum diameter. Efficient motility and penetration depend on active flagellar beating. To understand how active beating of the flagellum affects the cell body, we genetically engineered T. brucei to produce anucleate cytoplasts (zoids and minis) with different flagellar attachment configurations and different swimming behaviors. We used cryo-electron tomography (cryo-ET) to visualize zoids and minis vitrified in different motility states. We showed that flagellar wave patterns reflective of their motility states are coupled to cytoskeleton deformation. Based on these observations, we propose a mechanism for how flagellum beating can deform the cell body via a flexible connection between the flagellar axoneme and the cell body. This mechanism may be critical for T. brucei to disseminate in its host through size-limiting barriers. |
format | Online Article Text |
id | pubmed-6042131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-60421312018-07-13 Flagellum couples cell shape to motility in Trypanosoma brucei Sun, Stella Y. Kaelber, Jason T. Chen, Muyuan Dong, Xiaoduo Nematbakhsh, Yasaman Shi, Jian Dougherty, Matthew Lim, Chwee Teck Schmid, Michael F. Chiu, Wah He, Cynthia Y. Proc Natl Acad Sci U S A PNAS Plus In the unicellular parasite Trypanosoma brucei, the causative agent of human African sleeping sickness, complex swimming behavior is driven by a flagellum laterally attached to the long and slender cell body. Using microfluidic assays, we demonstrated that T. brucei can penetrate through an orifice smaller than its maximum diameter. Efficient motility and penetration depend on active flagellar beating. To understand how active beating of the flagellum affects the cell body, we genetically engineered T. brucei to produce anucleate cytoplasts (zoids and minis) with different flagellar attachment configurations and different swimming behaviors. We used cryo-electron tomography (cryo-ET) to visualize zoids and minis vitrified in different motility states. We showed that flagellar wave patterns reflective of their motility states are coupled to cytoskeleton deformation. Based on these observations, we propose a mechanism for how flagellum beating can deform the cell body via a flexible connection between the flagellar axoneme and the cell body. This mechanism may be critical for T. brucei to disseminate in its host through size-limiting barriers. National Academy of Sciences 2018-06-26 2018-06-11 /pmc/articles/PMC6042131/ /pubmed/29891682 http://dx.doi.org/10.1073/pnas.1722618115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | PNAS Plus Sun, Stella Y. Kaelber, Jason T. Chen, Muyuan Dong, Xiaoduo Nematbakhsh, Yasaman Shi, Jian Dougherty, Matthew Lim, Chwee Teck Schmid, Michael F. Chiu, Wah He, Cynthia Y. Flagellum couples cell shape to motility in Trypanosoma brucei |
title | Flagellum couples cell shape to motility in Trypanosoma brucei |
title_full | Flagellum couples cell shape to motility in Trypanosoma brucei |
title_fullStr | Flagellum couples cell shape to motility in Trypanosoma brucei |
title_full_unstemmed | Flagellum couples cell shape to motility in Trypanosoma brucei |
title_short | Flagellum couples cell shape to motility in Trypanosoma brucei |
title_sort | flagellum couples cell shape to motility in trypanosoma brucei |
topic | PNAS Plus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042131/ https://www.ncbi.nlm.nih.gov/pubmed/29891682 http://dx.doi.org/10.1073/pnas.1722618115 |
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