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High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites

Cellular motility is an ancient eukaryotic trait, ubiquitous across phyla with roles in predator avoidance, resource access, and competition. Flagellar motility is seen in various parasitic protozoans, and morphological changes in flagella during the parasite life cycle have been observed. We studie...

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Autores principales: Findlay, Rachel C, Osman, Mohamed, Spence, Kirstin A, Kaye, Paul M, Walrad, Pegine B, Wilson, Laurence G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238501/
https://www.ncbi.nlm.nih.gov/pubmed/34180835
http://dx.doi.org/10.7554/eLife.65051
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author Findlay, Rachel C
Osman, Mohamed
Spence, Kirstin A
Kaye, Paul M
Walrad, Pegine B
Wilson, Laurence G
author_facet Findlay, Rachel C
Osman, Mohamed
Spence, Kirstin A
Kaye, Paul M
Walrad, Pegine B
Wilson, Laurence G
author_sort Findlay, Rachel C
collection PubMed
description Cellular motility is an ancient eukaryotic trait, ubiquitous across phyla with roles in predator avoidance, resource access, and competition. Flagellar motility is seen in various parasitic protozoans, and morphological changes in flagella during the parasite life cycle have been observed. We studied the impact of these changes on motility across life cycle stages, and how such changes might serve to facilitate human infection. We used holographic microscopy to image swimming cells of different Leishmania mexicana life cycle stages in three dimensions. We find that the human-infective (metacyclic promastigote) forms display ‘run and tumble’ behaviour in the absence of stimulus, reminiscent of bacterial motion, and that they specifically modify swimming direction and speed to target host immune cells in response to a macrophage-derived stimulus. Non-infective (procyclic promastigote) cells swim more slowly, along meandering helical paths. These findings demonstrate adaptation of swimming phenotype and chemotaxis towards human cells.
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spelling pubmed-82385012021-06-30 High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites Findlay, Rachel C Osman, Mohamed Spence, Kirstin A Kaye, Paul M Walrad, Pegine B Wilson, Laurence G eLife Microbiology and Infectious Disease Cellular motility is an ancient eukaryotic trait, ubiquitous across phyla with roles in predator avoidance, resource access, and competition. Flagellar motility is seen in various parasitic protozoans, and morphological changes in flagella during the parasite life cycle have been observed. We studied the impact of these changes on motility across life cycle stages, and how such changes might serve to facilitate human infection. We used holographic microscopy to image swimming cells of different Leishmania mexicana life cycle stages in three dimensions. We find that the human-infective (metacyclic promastigote) forms display ‘run and tumble’ behaviour in the absence of stimulus, reminiscent of bacterial motion, and that they specifically modify swimming direction and speed to target host immune cells in response to a macrophage-derived stimulus. Non-infective (procyclic promastigote) cells swim more slowly, along meandering helical paths. These findings demonstrate adaptation of swimming phenotype and chemotaxis towards human cells. eLife Sciences Publications, Ltd 2021-06-28 /pmc/articles/PMC8238501/ /pubmed/34180835 http://dx.doi.org/10.7554/eLife.65051 Text en © 2021, Findlay et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
Findlay, Rachel C
Osman, Mohamed
Spence, Kirstin A
Kaye, Paul M
Walrad, Pegine B
Wilson, Laurence G
High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites
title High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites
title_full High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites
title_fullStr High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites
title_full_unstemmed High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites
title_short High-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective Leishmania parasites
title_sort high-speed, three-dimensional imaging reveals chemotactic behaviour specific to human-infective leishmania parasites
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238501/
https://www.ncbi.nlm.nih.gov/pubmed/34180835
http://dx.doi.org/10.7554/eLife.65051
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