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Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae
Filamentous hyphae of the human pathogen, Candida albicans, invade mucosal layers and medical silicones. In vitro, hyphal tips reorient thigmotropically on contact with small obstacles. It is not known how surface topography is sensed but hyphae lacking the cortical marker, Rsr1/Bud1, are unresponsi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371639/ https://www.ncbi.nlm.nih.gov/pubmed/25262778 http://dx.doi.org/10.1111/cmi.12369 |
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author | Thomson, Darren D Wehmeier, Silvia Byfield, FitzRoy J Janmey, Paul A Caballero-Lima, David Crossley, Alison Brand, Alexandra C |
author_facet | Thomson, Darren D Wehmeier, Silvia Byfield, FitzRoy J Janmey, Paul A Caballero-Lima, David Crossley, Alison Brand, Alexandra C |
author_sort | Thomson, Darren D |
collection | PubMed |
description | Filamentous hyphae of the human pathogen, Candida albicans, invade mucosal layers and medical silicones. In vitro, hyphal tips reorient thigmotropically on contact with small obstacles. It is not known how surface topography is sensed but hyphae lacking the cortical marker, Rsr1/Bud1, are unresponsive. We show that, on surfaces, the morphology of hyphal tips and the position of internal polarity protein complexes are asymmetrically skewed towards the substratum and biased towards the softer of two surfaces. In nano-fabricated chambers, the Spitzenkörper (Spk) responded to touch by translocating across the apex towards the point of contact, where its stable maintenance correlated with contour-following growth. In the rsr1Δ mutant, the position of the Spk meandered and these responses were attenuated. Perpendicular collision caused lateral Spk oscillation within the tip until after establishment of a new growth axis, suggesting Spk position does not predict the direction of growth in C. albicans. Acute tip reorientation occurred only in cells where forward growth was countered by hyphal friction sufficient to generate a tip force of ∼ 8.7 μN (1.2 MPa), more than that required to penetrate host cell membranes. These findings suggest mechanisms through which the organization of hyphal tip growth in C. albicans facilitates the probing, penetration and invasion of host tissue. |
format | Online Article Text |
id | pubmed-4371639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43716392015-03-26 Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae Thomson, Darren D Wehmeier, Silvia Byfield, FitzRoy J Janmey, Paul A Caballero-Lima, David Crossley, Alison Brand, Alexandra C Cell Microbiol Original Articles Filamentous hyphae of the human pathogen, Candida albicans, invade mucosal layers and medical silicones. In vitro, hyphal tips reorient thigmotropically on contact with small obstacles. It is not known how surface topography is sensed but hyphae lacking the cortical marker, Rsr1/Bud1, are unresponsive. We show that, on surfaces, the morphology of hyphal tips and the position of internal polarity protein complexes are asymmetrically skewed towards the substratum and biased towards the softer of two surfaces. In nano-fabricated chambers, the Spitzenkörper (Spk) responded to touch by translocating across the apex towards the point of contact, where its stable maintenance correlated with contour-following growth. In the rsr1Δ mutant, the position of the Spk meandered and these responses were attenuated. Perpendicular collision caused lateral Spk oscillation within the tip until after establishment of a new growth axis, suggesting Spk position does not predict the direction of growth in C. albicans. Acute tip reorientation occurred only in cells where forward growth was countered by hyphal friction sufficient to generate a tip force of ∼ 8.7 μN (1.2 MPa), more than that required to penetrate host cell membranes. These findings suggest mechanisms through which the organization of hyphal tip growth in C. albicans facilitates the probing, penetration and invasion of host tissue. BlackWell Publishing Ltd 2015-03 2014-11-25 /pmc/articles/PMC4371639/ /pubmed/25262778 http://dx.doi.org/10.1111/cmi.12369 Text en © 2014 The Authors. Cellular Microbiology published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Thomson, Darren D Wehmeier, Silvia Byfield, FitzRoy J Janmey, Paul A Caballero-Lima, David Crossley, Alison Brand, Alexandra C Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae |
title | Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae |
title_full | Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae |
title_fullStr | Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae |
title_full_unstemmed | Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae |
title_short | Contact-induced apical asymmetry drives the thigmotropic responses of Candida albicans hyphae |
title_sort | contact-induced apical asymmetry drives the thigmotropic responses of candida albicans hyphae |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371639/ https://www.ncbi.nlm.nih.gov/pubmed/25262778 http://dx.doi.org/10.1111/cmi.12369 |
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