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Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes

The collective movement of African trypanosomes on semi-solid surfaces, known as social motility, is presumed to be due to migration factors and repellents released by the parasites. Here we show that procyclic (insect midgut) forms acidify their environment as a consequence of glucose metabolism, g...

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Autores principales: Shaw, Sebastian, Knüsel, Sebastian, Abbühl, Daniel, Naguleswaran, Arunasalam, Etzensperger, Ruth, Benninger, Mattias, Roditi, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807625/
https://www.ncbi.nlm.nih.gov/pubmed/35105902
http://dx.doi.org/10.1038/s41467-022-28293-w
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author Shaw, Sebastian
Knüsel, Sebastian
Abbühl, Daniel
Naguleswaran, Arunasalam
Etzensperger, Ruth
Benninger, Mattias
Roditi, Isabel
author_facet Shaw, Sebastian
Knüsel, Sebastian
Abbühl, Daniel
Naguleswaran, Arunasalam
Etzensperger, Ruth
Benninger, Mattias
Roditi, Isabel
author_sort Shaw, Sebastian
collection PubMed
description The collective movement of African trypanosomes on semi-solid surfaces, known as social motility, is presumed to be due to migration factors and repellents released by the parasites. Here we show that procyclic (insect midgut) forms acidify their environment as a consequence of glucose metabolism, generating pH gradients by diffusion. Early and late procyclic forms exhibit self-organising properties on agarose plates. While early procyclic forms are repelled by acid and migrate outwards, late procyclic forms remain at the inoculation site. Furthermore, trypanosomes respond to exogenously formed pH gradients, with both early and late procyclic forms being attracted to alkali. pH taxis is mediated by multiple cyclic AMP effectors: deletion of one copy of adenylate cyclase ACP5, or both copies of the cyclic AMP response protein CARP3, abrogates the response to acid, while deletion of phosphodiesterase PDEB1 completely abolishes pH taxis. The ability to sense pH is biologically relevant as trypanosomes experience large changes as they migrate through their tsetse host. Supporting this, a CARP3 null mutant is severely compromised in its ability to establish infections in flies. Based on these findings, we propose that the expanded family of adenylate cyclases in trypanosomes might govern other chemotactic responses in their two hosts.
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spelling pubmed-88076252022-02-07 Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes Shaw, Sebastian Knüsel, Sebastian Abbühl, Daniel Naguleswaran, Arunasalam Etzensperger, Ruth Benninger, Mattias Roditi, Isabel Nat Commun Article The collective movement of African trypanosomes on semi-solid surfaces, known as social motility, is presumed to be due to migration factors and repellents released by the parasites. Here we show that procyclic (insect midgut) forms acidify their environment as a consequence of glucose metabolism, generating pH gradients by diffusion. Early and late procyclic forms exhibit self-organising properties on agarose plates. While early procyclic forms are repelled by acid and migrate outwards, late procyclic forms remain at the inoculation site. Furthermore, trypanosomes respond to exogenously formed pH gradients, with both early and late procyclic forms being attracted to alkali. pH taxis is mediated by multiple cyclic AMP effectors: deletion of one copy of adenylate cyclase ACP5, or both copies of the cyclic AMP response protein CARP3, abrogates the response to acid, while deletion of phosphodiesterase PDEB1 completely abolishes pH taxis. The ability to sense pH is biologically relevant as trypanosomes experience large changes as they migrate through their tsetse host. Supporting this, a CARP3 null mutant is severely compromised in its ability to establish infections in flies. Based on these findings, we propose that the expanded family of adenylate cyclases in trypanosomes might govern other chemotactic responses in their two hosts. Nature Publishing Group UK 2022-02-01 /pmc/articles/PMC8807625/ /pubmed/35105902 http://dx.doi.org/10.1038/s41467-022-28293-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shaw, Sebastian
Knüsel, Sebastian
Abbühl, Daniel
Naguleswaran, Arunasalam
Etzensperger, Ruth
Benninger, Mattias
Roditi, Isabel
Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes
title Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes
title_full Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes
title_fullStr Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes
title_full_unstemmed Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes
title_short Cyclic AMP signalling and glucose metabolism mediate pH taxis by African trypanosomes
title_sort cyclic amp signalling and glucose metabolism mediate ph taxis by african trypanosomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807625/
https://www.ncbi.nlm.nih.gov/pubmed/35105902
http://dx.doi.org/10.1038/s41467-022-28293-w
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