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The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll

Parastagonospora nodorum is an economically important necrotrophic fungal pathogen of wheat. Parastagonospora nodorum secretes necrotrophic effectors that target wheat susceptibility genes to induce programmed cell death (PCD). In this study, we cloned and functionally validated SnTox5 and character...

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Autores principales: Kariyawasam, Gayan K., Richards, Jonathan K., Wyatt, Nathan A., Running, Katherine L. D., Xu, Steven S., Liu, Zhaohui, Borowicz, Pawel, Faris, Justin D., Friesen, Timothy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291777/
https://www.ncbi.nlm.nih.gov/pubmed/34231227
http://dx.doi.org/10.1111/nph.17602
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author Kariyawasam, Gayan K.
Richards, Jonathan K.
Wyatt, Nathan A.
Running, Katherine L. D.
Xu, Steven S.
Liu, Zhaohui
Borowicz, Pawel
Faris, Justin D.
Friesen, Timothy L.
author_facet Kariyawasam, Gayan K.
Richards, Jonathan K.
Wyatt, Nathan A.
Running, Katherine L. D.
Xu, Steven S.
Liu, Zhaohui
Borowicz, Pawel
Faris, Justin D.
Friesen, Timothy L.
author_sort Kariyawasam, Gayan K.
collection PubMed
description Parastagonospora nodorum is an economically important necrotrophic fungal pathogen of wheat. Parastagonospora nodorum secretes necrotrophic effectors that target wheat susceptibility genes to induce programmed cell death (PCD). In this study, we cloned and functionally validated SnTox5 and characterized its role in pathogenesis. We used whole genome sequencing, genome‐wide association study (GWAS) mapping, CRISPR‐Cas9‐based gene disruption, gain‐of‐function transformation, quantitative trait locus (QTL) analysis, haplotype and isoform analysis, protein modeling, quantitative PCR, and laser confocal microscopy to validate SnTox5 and functionally characterize SnTox5. SnTox5 is a mature 16.26 kDa protein with high structural similarity to SnTox3. Wild‐type and mutant P. nodorum strains and wheat genotypes of SnTox5 and Snn5, respectively, were used to show that SnTox5 not only targets Snn5 to induce PCD but also facilitates the colonization of the mesophyll layer even in the absence of Snn5. Here we show that SnTox5 facilitates the efficient colonization of the mesophyll tissue and elicits PCD specific to host lines carrying Snn5. The homology to SnTox3 and the ability of SnTox5 to facilitate the colonizing of the mesophyll also suggest a role in the suppression of host defense before PCD induction.
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spelling pubmed-92917772022-07-20 The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll Kariyawasam, Gayan K. Richards, Jonathan K. Wyatt, Nathan A. Running, Katherine L. D. Xu, Steven S. Liu, Zhaohui Borowicz, Pawel Faris, Justin D. Friesen, Timothy L. New Phytol Research Parastagonospora nodorum is an economically important necrotrophic fungal pathogen of wheat. Parastagonospora nodorum secretes necrotrophic effectors that target wheat susceptibility genes to induce programmed cell death (PCD). In this study, we cloned and functionally validated SnTox5 and characterized its role in pathogenesis. We used whole genome sequencing, genome‐wide association study (GWAS) mapping, CRISPR‐Cas9‐based gene disruption, gain‐of‐function transformation, quantitative trait locus (QTL) analysis, haplotype and isoform analysis, protein modeling, quantitative PCR, and laser confocal microscopy to validate SnTox5 and functionally characterize SnTox5. SnTox5 is a mature 16.26 kDa protein with high structural similarity to SnTox3. Wild‐type and mutant P. nodorum strains and wheat genotypes of SnTox5 and Snn5, respectively, were used to show that SnTox5 not only targets Snn5 to induce PCD but also facilitates the colonization of the mesophyll layer even in the absence of Snn5. Here we show that SnTox5 facilitates the efficient colonization of the mesophyll tissue and elicits PCD specific to host lines carrying Snn5. The homology to SnTox3 and the ability of SnTox5 to facilitate the colonizing of the mesophyll also suggest a role in the suppression of host defense before PCD induction. John Wiley and Sons Inc. 2021-08-03 2022-01 /pmc/articles/PMC9291777/ /pubmed/34231227 http://dx.doi.org/10.1111/nph.17602 Text en © No claim to US Government works New Phytologist © 2021 New Phytologist Foundation https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
Kariyawasam, Gayan K.
Richards, Jonathan K.
Wyatt, Nathan A.
Running, Katherine L. D.
Xu, Steven S.
Liu, Zhaohui
Borowicz, Pawel
Faris, Justin D.
Friesen, Timothy L.
The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll
title The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll
title_full The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll
title_fullStr The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll
title_full_unstemmed The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll
title_short The Parastagonospora nodorum necrotrophic effector SnTox5 targets the wheat gene Snn5 and facilitates entry into the leaf mesophyll
title_sort parastagonospora nodorum necrotrophic effector sntox5 targets the wheat gene snn5 and facilitates entry into the leaf mesophyll
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291777/
https://www.ncbi.nlm.nih.gov/pubmed/34231227
http://dx.doi.org/10.1111/nph.17602
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