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An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration
Filamentous plant pathogens apply mechanical forces to pierce their hosts surface and penetrate its tissues. Devastating Phytophthora pathogens harness a specialized form of invasive tip growth to slice through the plant surface, wielding their hypha as a microscopic knife. Slicing requires a sharp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187236/ https://www.ncbi.nlm.nih.gov/pubmed/35687685 http://dx.doi.org/10.1126/sciadv.abo0875 |
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author | Bronkhorst, Jochem Kots, Kiki de Jong, Djanick Kasteel, Michiel van Boxmeer, Thomas Joemmanbaks, Tanweer Govers, Francine van der Gucht, Jasper Ketelaar, Tijs Sprakel, Joris |
author_facet | Bronkhorst, Jochem Kots, Kiki de Jong, Djanick Kasteel, Michiel van Boxmeer, Thomas Joemmanbaks, Tanweer Govers, Francine van der Gucht, Jasper Ketelaar, Tijs Sprakel, Joris |
author_sort | Bronkhorst, Jochem |
collection | PubMed |
description | Filamentous plant pathogens apply mechanical forces to pierce their hosts surface and penetrate its tissues. Devastating Phytophthora pathogens harness a specialized form of invasive tip growth to slice through the plant surface, wielding their hypha as a microscopic knife. Slicing requires a sharp hyphal tip that is not blunted at the site of the mechanical interaction. How tip shape is controlled, however, is unknown. We uncover an actin-based mechanostat in Phytophthora infestans that controls tip sharpness during penetration. Mechanical stimulation of the hypha leads to the emergence of an aster-like actin configuration, which shows fast, local, and quantitative feedback to the local stress. We evidence that this functions as an adaptive mechanical scaffold that sharpens the invasive weapon and prevents it from blunting. The hyphal tip mechanostat enables the efficient conversion of turgor into localized invasive pressures that are required to achieve host penetration. |
format | Online Article Text |
id | pubmed-9187236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91872362022-06-21 An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration Bronkhorst, Jochem Kots, Kiki de Jong, Djanick Kasteel, Michiel van Boxmeer, Thomas Joemmanbaks, Tanweer Govers, Francine van der Gucht, Jasper Ketelaar, Tijs Sprakel, Joris Sci Adv Biomedicine and Life Sciences Filamentous plant pathogens apply mechanical forces to pierce their hosts surface and penetrate its tissues. Devastating Phytophthora pathogens harness a specialized form of invasive tip growth to slice through the plant surface, wielding their hypha as a microscopic knife. Slicing requires a sharp hyphal tip that is not blunted at the site of the mechanical interaction. How tip shape is controlled, however, is unknown. We uncover an actin-based mechanostat in Phytophthora infestans that controls tip sharpness during penetration. Mechanical stimulation of the hypha leads to the emergence of an aster-like actin configuration, which shows fast, local, and quantitative feedback to the local stress. We evidence that this functions as an adaptive mechanical scaffold that sharpens the invasive weapon and prevents it from blunting. The hyphal tip mechanostat enables the efficient conversion of turgor into localized invasive pressures that are required to achieve host penetration. American Association for the Advancement of Science 2022-06-10 /pmc/articles/PMC9187236/ /pubmed/35687685 http://dx.doi.org/10.1126/sciadv.abo0875 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Bronkhorst, Jochem Kots, Kiki de Jong, Djanick Kasteel, Michiel van Boxmeer, Thomas Joemmanbaks, Tanweer Govers, Francine van der Gucht, Jasper Ketelaar, Tijs Sprakel, Joris An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration |
title | An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration |
title_full | An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration |
title_fullStr | An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration |
title_full_unstemmed | An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration |
title_short | An actin mechanostat ensures hyphal tip sharpness in Phytophthora infestans to achieve host penetration |
title_sort | actin mechanostat ensures hyphal tip sharpness in phytophthora infestans to achieve host penetration |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187236/ https://www.ncbi.nlm.nih.gov/pubmed/35687685 http://dx.doi.org/10.1126/sciadv.abo0875 |
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