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Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference

The causative agent of white mold, Sclerotinia sclerotiorum, is capable of infecting over 600 plant species and is responsible for significant crop losses across the globe. Control is currently dependent on broad-spectrum chemical agents that can negatively impact the agroecological environment, pre...

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Autores principales: Walker, Philip L., Ziegler, Dylan J., Giesbrecht, Shayna, McLoughlin, Austein, Wan, Joey, Khan, Deirdre, Hoi, Vanessa, Whyard, Steve, Belmonte, Mark F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119085/
https://www.ncbi.nlm.nih.gov/pubmed/37081036
http://dx.doi.org/10.1038/s41598-023-33335-4
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author Walker, Philip L.
Ziegler, Dylan J.
Giesbrecht, Shayna
McLoughlin, Austein
Wan, Joey
Khan, Deirdre
Hoi, Vanessa
Whyard, Steve
Belmonte, Mark F.
author_facet Walker, Philip L.
Ziegler, Dylan J.
Giesbrecht, Shayna
McLoughlin, Austein
Wan, Joey
Khan, Deirdre
Hoi, Vanessa
Whyard, Steve
Belmonte, Mark F.
author_sort Walker, Philip L.
collection PubMed
description The causative agent of white mold, Sclerotinia sclerotiorum, is capable of infecting over 600 plant species and is responsible for significant crop losses across the globe. Control is currently dependent on broad-spectrum chemical agents that can negatively impact the agroecological environment, presenting a need to develop alternative control measures. In this study, we developed transgenic Arabidopsis thaliana (AT1703) expressing hairpin (hp)RNA to silence S. sclerotiorum ABHYDROLASE-3 and slow infection through host induced gene silencing (HIGS). Leaf infection assays show reduced S. sclerotiorum lesion size, fungal load, and ABHYDROLASE-3 transcript abundance in AT1703 compared to wild-type Col-0. To better understand how HIGS influences host–pathogen interactions, we performed global RNA sequencing on AT1703 and wild-type Col-0 directly at the site of S. sclerotiorum infection. RNA sequencing data reveals enrichment of the salicylic acid (SA)-mediated systemic acquired resistance (SAR) pathway, as well as transcription factors predicted to regulate plant immunity. Using RT-qPCR, we identified predicted interacting partners of ABHYDROLASE-3 in the polyamine synthesis pathway of S. sclerotiorum that demonstrate co-reduction with ABHYDROLASE-3 transcript levels during infection. Together, these results demonstrate the utility of HIGS technology in slowing S. sclerotiorum infection and provide insight into the role of ABHYDROLASE-3 in the A. thaliana–S. sclerotiorum pathosystem.
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spelling pubmed-101190852023-04-22 Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference Walker, Philip L. Ziegler, Dylan J. Giesbrecht, Shayna McLoughlin, Austein Wan, Joey Khan, Deirdre Hoi, Vanessa Whyard, Steve Belmonte, Mark F. Sci Rep Article The causative agent of white mold, Sclerotinia sclerotiorum, is capable of infecting over 600 plant species and is responsible for significant crop losses across the globe. Control is currently dependent on broad-spectrum chemical agents that can negatively impact the agroecological environment, presenting a need to develop alternative control measures. In this study, we developed transgenic Arabidopsis thaliana (AT1703) expressing hairpin (hp)RNA to silence S. sclerotiorum ABHYDROLASE-3 and slow infection through host induced gene silencing (HIGS). Leaf infection assays show reduced S. sclerotiorum lesion size, fungal load, and ABHYDROLASE-3 transcript abundance in AT1703 compared to wild-type Col-0. To better understand how HIGS influences host–pathogen interactions, we performed global RNA sequencing on AT1703 and wild-type Col-0 directly at the site of S. sclerotiorum infection. RNA sequencing data reveals enrichment of the salicylic acid (SA)-mediated systemic acquired resistance (SAR) pathway, as well as transcription factors predicted to regulate plant immunity. Using RT-qPCR, we identified predicted interacting partners of ABHYDROLASE-3 in the polyamine synthesis pathway of S. sclerotiorum that demonstrate co-reduction with ABHYDROLASE-3 transcript levels during infection. Together, these results demonstrate the utility of HIGS technology in slowing S. sclerotiorum infection and provide insight into the role of ABHYDROLASE-3 in the A. thaliana–S. sclerotiorum pathosystem. Nature Publishing Group UK 2023-04-20 /pmc/articles/PMC10119085/ /pubmed/37081036 http://dx.doi.org/10.1038/s41598-023-33335-4 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Walker, Philip L.
Ziegler, Dylan J.
Giesbrecht, Shayna
McLoughlin, Austein
Wan, Joey
Khan, Deirdre
Hoi, Vanessa
Whyard, Steve
Belmonte, Mark F.
Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference
title Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference
title_full Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference
title_fullStr Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference
title_full_unstemmed Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference
title_short Control of white mold (Sclerotinia sclerotiorum) through plant-mediated RNA interference
title_sort control of white mold (sclerotinia sclerotiorum) through plant-mediated rna interference
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119085/
https://www.ncbi.nlm.nih.gov/pubmed/37081036
http://dx.doi.org/10.1038/s41598-023-33335-4
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