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Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions

The human pathogenic amoeba Acanthamoeba castellanii (A. castellanii) causes severe diseases, including acanthamoeba keratitis and encephalitis. Pathogenicity arises from the killing of target-cells by an extracellular killing mechanism, where the crucial first step is the formation of a close conta...

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Autores principales: Huth, Steven, Reverey, Julia F., Leippe, Matthias, Selhuber-Unkel, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417443/
https://www.ncbi.nlm.nih.gov/pubmed/28472161
http://dx.doi.org/10.1371/journal.pone.0176207
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author Huth, Steven
Reverey, Julia F.
Leippe, Matthias
Selhuber-Unkel, Christine
author_facet Huth, Steven
Reverey, Julia F.
Leippe, Matthias
Selhuber-Unkel, Christine
author_sort Huth, Steven
collection PubMed
description The human pathogenic amoeba Acanthamoeba castellanii (A. castellanii) causes severe diseases, including acanthamoeba keratitis and encephalitis. Pathogenicity arises from the killing of target-cells by an extracellular killing mechanism, where the crucial first step is the formation of a close contact between A. castellanii and the target-cell. This process is mediated by the glycocalix of the target-cell and mannose has been identified as key mediator. The aim of the present study was to carry out a detailed biophysical investigation of mannose-mediated adhesion of A. castellanii using force spectroscopy on single trophozoites. In detail, we studied the interaction of a mannose-coated cantilever with an A. castellanii trophozoite, as mannose is the decisive part of the cellular glycocalix in mediating pathogenicity. We observed a clear increase of the force to initiate cantilever detachment from the trophozoite with increasing contact time. This increase is also associated with an increase in the work of detachment. Furthermore, we also analyzed single rupture events during the detachment process and found that single rupture processes are associated with membrane tether formation, suggesting that the cytoskeleton is not involved in mannose binding events during the first few seconds of contact. Our study provides an experimental and conceptual basis for measuring interactions between pathogens and target-cells at different levels of complexity and as a function of interaction time, thus leading to new insights into the biophysical mechanisms of parasite pathogenicity.
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spelling pubmed-54174432017-05-14 Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions Huth, Steven Reverey, Julia F. Leippe, Matthias Selhuber-Unkel, Christine PLoS One Research Article The human pathogenic amoeba Acanthamoeba castellanii (A. castellanii) causes severe diseases, including acanthamoeba keratitis and encephalitis. Pathogenicity arises from the killing of target-cells by an extracellular killing mechanism, where the crucial first step is the formation of a close contact between A. castellanii and the target-cell. This process is mediated by the glycocalix of the target-cell and mannose has been identified as key mediator. The aim of the present study was to carry out a detailed biophysical investigation of mannose-mediated adhesion of A. castellanii using force spectroscopy on single trophozoites. In detail, we studied the interaction of a mannose-coated cantilever with an A. castellanii trophozoite, as mannose is the decisive part of the cellular glycocalix in mediating pathogenicity. We observed a clear increase of the force to initiate cantilever detachment from the trophozoite with increasing contact time. This increase is also associated with an increase in the work of detachment. Furthermore, we also analyzed single rupture events during the detachment process and found that single rupture processes are associated with membrane tether formation, suggesting that the cytoskeleton is not involved in mannose binding events during the first few seconds of contact. Our study provides an experimental and conceptual basis for measuring interactions between pathogens and target-cells at different levels of complexity and as a function of interaction time, thus leading to new insights into the biophysical mechanisms of parasite pathogenicity. Public Library of Science 2017-05-04 /pmc/articles/PMC5417443/ /pubmed/28472161 http://dx.doi.org/10.1371/journal.pone.0176207 Text en © 2017 Huth 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Huth, Steven
Reverey, Julia F.
Leippe, Matthias
Selhuber-Unkel, Christine
Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions
title Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions
title_full Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions
title_fullStr Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions
title_full_unstemmed Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions
title_short Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions
title_sort adhesion forces and mechanics in mannose-mediated acanthamoeba interactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417443/
https://www.ncbi.nlm.nih.gov/pubmed/28472161
http://dx.doi.org/10.1371/journal.pone.0176207
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