Cargando…

Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional

Microorganisms, particularly parasites, have developed sophisticated swimming mechanisms to cope with a varied range of environments. African Trypanosomes, causative agents of fatal illness in humans and animals, use an insect vector (the Tsetse fly) to infect mammals, involving many developmental c...

Descripción completa

Detalles Bibliográficos
Autores principales: Uppaluri, Sravanti, Nagler, Jan, Stellamanns, Eric, Heddergott, Niko, Herminghaus, Stephan, Engstler, Markus, Pfohl, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116898/
https://www.ncbi.nlm.nih.gov/pubmed/21698122
http://dx.doi.org/10.1371/journal.pcbi.1002058
_version_ 1782206298656342016
author Uppaluri, Sravanti
Nagler, Jan
Stellamanns, Eric
Heddergott, Niko
Herminghaus, Stephan
Engstler, Markus
Pfohl, Thomas
author_facet Uppaluri, Sravanti
Nagler, Jan
Stellamanns, Eric
Heddergott, Niko
Herminghaus, Stephan
Engstler, Markus
Pfohl, Thomas
author_sort Uppaluri, Sravanti
collection PubMed
description Microorganisms, particularly parasites, have developed sophisticated swimming mechanisms to cope with a varied range of environments. African Trypanosomes, causative agents of fatal illness in humans and animals, use an insect vector (the Tsetse fly) to infect mammals, involving many developmental changes in which cell motility is of prime importance. Our studies reveal that differences in cell body shape are correlated with a diverse range of cell behaviors contributing to the directional motion of the cell. Straighter cells swim more directionally while cells that exhibit little net displacement appear to be more bent. Initiation of cell division, beginning with the emergence of a second flagellum at the base, correlates to directional persistence. Cell trajectory and rapid body fluctuation correlation analysis uncovers two characteristic relaxation times: a short relaxation time due to strong body distortions in the range of 20 to 80 ms and a longer time associated with the persistence in average swimming direction in the order of 15 seconds. Different motility modes, possibly resulting from varying body stiffness, could be of consequence for host invasion during distinct infective stages.
format Online
Article
Text
id pubmed-3116898
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-31168982011-06-22 Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional Uppaluri, Sravanti Nagler, Jan Stellamanns, Eric Heddergott, Niko Herminghaus, Stephan Engstler, Markus Pfohl, Thomas PLoS Comput Biol Research Article Microorganisms, particularly parasites, have developed sophisticated swimming mechanisms to cope with a varied range of environments. African Trypanosomes, causative agents of fatal illness in humans and animals, use an insect vector (the Tsetse fly) to infect mammals, involving many developmental changes in which cell motility is of prime importance. Our studies reveal that differences in cell body shape are correlated with a diverse range of cell behaviors contributing to the directional motion of the cell. Straighter cells swim more directionally while cells that exhibit little net displacement appear to be more bent. Initiation of cell division, beginning with the emergence of a second flagellum at the base, correlates to directional persistence. Cell trajectory and rapid body fluctuation correlation analysis uncovers two characteristic relaxation times: a short relaxation time due to strong body distortions in the range of 20 to 80 ms and a longer time associated with the persistence in average swimming direction in the order of 15 seconds. Different motility modes, possibly resulting from varying body stiffness, could be of consequence for host invasion during distinct infective stages. Public Library of Science 2011-06-16 /pmc/articles/PMC3116898/ /pubmed/21698122 http://dx.doi.org/10.1371/journal.pcbi.1002058 Text en Uppaluri et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Uppaluri, Sravanti
Nagler, Jan
Stellamanns, Eric
Heddergott, Niko
Herminghaus, Stephan
Engstler, Markus
Pfohl, Thomas
Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional
title Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional
title_full Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional
title_fullStr Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional
title_full_unstemmed Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional
title_short Impact of Microscopic Motility on the Swimming Behavior of Parasites: Straighter Trypanosomes are More Directional
title_sort impact of microscopic motility on the swimming behavior of parasites: straighter trypanosomes are more directional
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116898/
https://www.ncbi.nlm.nih.gov/pubmed/21698122
http://dx.doi.org/10.1371/journal.pcbi.1002058
work_keys_str_mv AT uppalurisravanti impactofmicroscopicmotilityontheswimmingbehaviorofparasitesstraightertrypanosomesaremoredirectional
AT naglerjan impactofmicroscopicmotilityontheswimmingbehaviorofparasitesstraightertrypanosomesaremoredirectional
AT stellamannseric impactofmicroscopicmotilityontheswimmingbehaviorofparasitesstraightertrypanosomesaremoredirectional
AT heddergottniko impactofmicroscopicmotilityontheswimmingbehaviorofparasitesstraightertrypanosomesaremoredirectional
AT herminghausstephan impactofmicroscopicmotilityontheswimmingbehaviorofparasitesstraightertrypanosomesaremoredirectional
AT engstlermarkus impactofmicroscopicmotilityontheswimmingbehaviorofparasitesstraightertrypanosomesaremoredirectional
AT pfohlthomas impactofmicroscopicmotilityontheswimmingbehaviorofparasitesstraightertrypanosomesaremoredirectional