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Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress
Fungi have evolved an array of spore discharge and dispersal processes. Here, we developed a theoretical model that explains the ejection mechanics of aeciospore liberation in the stem rust pathogen Puccinia graminis. Aeciospores are released from cluster cups formed on its Berberis host, spreading...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536709/ https://www.ncbi.nlm.nih.gov/pubmed/34686772 http://dx.doi.org/10.1038/s42003-021-02747-1 |
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author | Bueno-Sancho, Vanessa Orton, Elizabeth S. Gerrity, Morgan Lewis, Clare M. Davey, Phoebe Findlay, Kim C. Barclay, Elaine Robinson, Phil Morris, Richard J. Blyth, Mark Saunders, Diane G. O. |
author_facet | Bueno-Sancho, Vanessa Orton, Elizabeth S. Gerrity, Morgan Lewis, Clare M. Davey, Phoebe Findlay, Kim C. Barclay, Elaine Robinson, Phil Morris, Richard J. Blyth, Mark Saunders, Diane G. O. |
author_sort | Bueno-Sancho, Vanessa |
collection | PubMed |
description | Fungi have evolved an array of spore discharge and dispersal processes. Here, we developed a theoretical model that explains the ejection mechanics of aeciospore liberation in the stem rust pathogen Puccinia graminis. Aeciospores are released from cluster cups formed on its Berberis host, spreading early-season inoculum into neighboring small-grain crops. Our model illustrates that during dew or rainfall, changes in aeciospore turgidity exerts substantial force on neighboring aeciospores in cluster cups whilst gaps between spores become perfused with water. This perfusion coats aeciospores with a lubrication film that facilitates expulsion, with single aeciospores reaching speeds of 0.053 to 0.754 m·s(−1). We also used aeciospore source strength estimates to simulate the aeciospore dispersal gradient and incorporated this into a publicly available web interface. This aids farmers and legislators to assess current local risk of dispersal and facilitates development of sophisticated epidemiological models to potentially curtail stem rust epidemics originating on Berberis. |
format | Online Article Text |
id | pubmed-8536709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85367092021-11-15 Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress Bueno-Sancho, Vanessa Orton, Elizabeth S. Gerrity, Morgan Lewis, Clare M. Davey, Phoebe Findlay, Kim C. Barclay, Elaine Robinson, Phil Morris, Richard J. Blyth, Mark Saunders, Diane G. O. Commun Biol Article Fungi have evolved an array of spore discharge and dispersal processes. Here, we developed a theoretical model that explains the ejection mechanics of aeciospore liberation in the stem rust pathogen Puccinia graminis. Aeciospores are released from cluster cups formed on its Berberis host, spreading early-season inoculum into neighboring small-grain crops. Our model illustrates that during dew or rainfall, changes in aeciospore turgidity exerts substantial force on neighboring aeciospores in cluster cups whilst gaps between spores become perfused with water. This perfusion coats aeciospores with a lubrication film that facilitates expulsion, with single aeciospores reaching speeds of 0.053 to 0.754 m·s(−1). We also used aeciospore source strength estimates to simulate the aeciospore dispersal gradient and incorporated this into a publicly available web interface. This aids farmers and legislators to assess current local risk of dispersal and facilitates development of sophisticated epidemiological models to potentially curtail stem rust epidemics originating on Berberis. Nature Publishing Group UK 2021-10-22 /pmc/articles/PMC8536709/ /pubmed/34686772 http://dx.doi.org/10.1038/s42003-021-02747-1 Text en © The Author(s) 2021 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 Bueno-Sancho, Vanessa Orton, Elizabeth S. Gerrity, Morgan Lewis, Clare M. Davey, Phoebe Findlay, Kim C. Barclay, Elaine Robinson, Phil Morris, Richard J. Blyth, Mark Saunders, Diane G. O. Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress |
title | Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress |
title_full | Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress |
title_fullStr | Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress |
title_full_unstemmed | Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress |
title_short | Aeciospore ejection in the rust pathogen Puccinia graminis is driven by moisture ingress |
title_sort | aeciospore ejection in the rust pathogen puccinia graminis is driven by moisture ingress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536709/ https://www.ncbi.nlm.nih.gov/pubmed/34686772 http://dx.doi.org/10.1038/s42003-021-02747-1 |
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