Cargando…

Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei

To complete its infectious cycle, the protozoan parasite Trypanosoma brucei must navigate through diverse tissue environments in both its tsetse fly and mammalian hosts. This is hypothesized to be driven by yet unidentified chemotactic cues. Prior work has shown that parasites engaging in social mot...

Descripción completa

Detalles Bibliográficos
Autores principales: DeMarco, Stephanie F., Saada, Edwin A., Lopez, Miguel A., Hill, Kent L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426175/
https://www.ncbi.nlm.nih.gov/pubmed/32817459
http://dx.doi.org/10.1128/mSphere.00685-20
_version_ 1783570631624753152
author DeMarco, Stephanie F.
Saada, Edwin A.
Lopez, Miguel A.
Hill, Kent L.
author_facet DeMarco, Stephanie F.
Saada, Edwin A.
Lopez, Miguel A.
Hill, Kent L.
author_sort DeMarco, Stephanie F.
collection PubMed
description To complete its infectious cycle, the protozoan parasite Trypanosoma brucei must navigate through diverse tissue environments in both its tsetse fly and mammalian hosts. This is hypothesized to be driven by yet unidentified chemotactic cues. Prior work has shown that parasites engaging in social motility in vitro alter their trajectory to avoid other groups of parasites, an example of negative chemotaxis. However, movement of T. brucei toward a stimulus, positive chemotaxis, has so far not been reported. Here, we show that upon encountering Escherichia coli, socially behaving T. brucei parasites exhibit positive chemotaxis, redirecting group movement toward the neighboring bacterial colony. This response occurs at a distance from the bacteria and involves active changes in parasite motility. By developing a quantitative chemotaxis assay, we show that the attractant is a soluble, diffusible signal dependent on actively growing E. coli. Time-lapse and live video microscopy revealed that T. brucei chemotaxis involves changes in both group and single cell motility. Groups of parasites change direction of group movement and accelerate as they approach the source of attractant, and this correlates with increasingly constrained movement of individual cells within the group. Identification of positive chemotaxis in T. brucei opens new opportunities to study mechanisms of chemotaxis in these medically and economically important pathogens. This will lead to deeper insights into how these parasites interact with and navigate through their host environments. IMPORTANCE Almost all living things need to be able to move, whether it is toward desirable environments or away from danger. For vector-borne parasites, successful transmission and infection require that these organisms be able to sense where they are and use signals from their environment to direct where they go next, a process known as chemotaxis. Here, we show that Trypanosoma brucei, the deadly protozoan parasite that causes African sleeping sickness, can sense and move toward an attractive cue. To our knowledge, this is the first report of positive chemotaxis in these organisms. In addition to describing a new behavior in T. brucei, our findings enable future studies of how chemotaxis works in these pathogens, which will lead to deeper understanding of how they move through their hosts and may lead to new therapeutic or transmission-blocking strategies.
format Online
Article
Text
id pubmed-7426175
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-74261752020-08-24 Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei DeMarco, Stephanie F. Saada, Edwin A. Lopez, Miguel A. Hill, Kent L. mSphere Research Article To complete its infectious cycle, the protozoan parasite Trypanosoma brucei must navigate through diverse tissue environments in both its tsetse fly and mammalian hosts. This is hypothesized to be driven by yet unidentified chemotactic cues. Prior work has shown that parasites engaging in social motility in vitro alter their trajectory to avoid other groups of parasites, an example of negative chemotaxis. However, movement of T. brucei toward a stimulus, positive chemotaxis, has so far not been reported. Here, we show that upon encountering Escherichia coli, socially behaving T. brucei parasites exhibit positive chemotaxis, redirecting group movement toward the neighboring bacterial colony. This response occurs at a distance from the bacteria and involves active changes in parasite motility. By developing a quantitative chemotaxis assay, we show that the attractant is a soluble, diffusible signal dependent on actively growing E. coli. Time-lapse and live video microscopy revealed that T. brucei chemotaxis involves changes in both group and single cell motility. Groups of parasites change direction of group movement and accelerate as they approach the source of attractant, and this correlates with increasingly constrained movement of individual cells within the group. Identification of positive chemotaxis in T. brucei opens new opportunities to study mechanisms of chemotaxis in these medically and economically important pathogens. This will lead to deeper insights into how these parasites interact with and navigate through their host environments. IMPORTANCE Almost all living things need to be able to move, whether it is toward desirable environments or away from danger. For vector-borne parasites, successful transmission and infection require that these organisms be able to sense where they are and use signals from their environment to direct where they go next, a process known as chemotaxis. Here, we show that Trypanosoma brucei, the deadly protozoan parasite that causes African sleeping sickness, can sense and move toward an attractive cue. To our knowledge, this is the first report of positive chemotaxis in these organisms. In addition to describing a new behavior in T. brucei, our findings enable future studies of how chemotaxis works in these pathogens, which will lead to deeper understanding of how they move through their hosts and may lead to new therapeutic or transmission-blocking strategies. American Society for Microbiology 2020-08-12 /pmc/articles/PMC7426175/ /pubmed/32817459 http://dx.doi.org/10.1128/mSphere.00685-20 Text en Copyright © 2020 DeMarco et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
DeMarco, Stephanie F.
Saada, Edwin A.
Lopez, Miguel A.
Hill, Kent L.
Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei
title Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei
title_full Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei
title_fullStr Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei
title_full_unstemmed Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei
title_short Identification of Positive Chemotaxis in the Protozoan Pathogen Trypanosoma brucei
title_sort identification of positive chemotaxis in the protozoan pathogen trypanosoma brucei
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426175/
https://www.ncbi.nlm.nih.gov/pubmed/32817459
http://dx.doi.org/10.1128/mSphere.00685-20
work_keys_str_mv AT demarcostephanief identificationofpositivechemotaxisintheprotozoanpathogentrypanosomabrucei
AT saadaedwina identificationofpositivechemotaxisintheprotozoanpathogentrypanosomabrucei
AT lopezmiguela identificationofpositivechemotaxisintheprotozoanpathogentrypanosomabrucei
AT hillkentl identificationofpositivechemotaxisintheprotozoanpathogentrypanosomabrucei