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Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana

Potato virus Y (PVY) is an aphid-transmitted potyvirus that affects economically important solanaceous species. In this study, the phenomena and mechanisms following infection with PVY were investigated in tobacco (Nicotiana benthamiana). In tobacco plants, infection with a mild strain of PVY (PVY(O...

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Autores principales: Kim, Won-Jin, Kim, Woong, Kim, Youngsoon, Cheong, Hyeonsook, Kim, Seok-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478736/
https://www.ncbi.nlm.nih.gov/pubmed/37655790
http://dx.doi.org/10.1080/15592324.2023.2252972
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author Kim, Won-Jin
Kim, Woong
Kim, Youngsoon
Cheong, Hyeonsook
Kim, Seok-Jun
author_facet Kim, Won-Jin
Kim, Woong
Kim, Youngsoon
Cheong, Hyeonsook
Kim, Seok-Jun
author_sort Kim, Won-Jin
collection PubMed
description Potato virus Y (PVY) is an aphid-transmitted potyvirus that affects economically important solanaceous species. In this study, the phenomena and mechanisms following infection with PVY were investigated in tobacco (Nicotiana benthamiana). In tobacco plants, infection with a mild strain of PVY (PVY(O)) induced stunted growth in the first two leaves at the shoot apex starting 7 days post-infection (dpi), and mosaic symptoms began to appear on newly developing young leaves at 14 dpi. Using enzyme-linked immunosorbent assay and ultrastructure analysis, we confirmed that viral particles accumulated only in the upper developing leaves of infected plants. We analyzed reactive oxygen species (ROS) generation in leaves from the bottom to the top of the plants to investigate whether delayed symptom development in leaves was associated with a defense response to the virus. In addition, the ultrastructural analysis confirmed the increase of ATG4 and ATG8, which are autophagy markers by endoplasmic reticulum (ER) stress, and the expression of genes involved in viral RNA suppression. Overall, our results suggested that viral RNA silencing and induced autophagy may play a role in the inhibition of viral symptom development in host plants in response to PVY(O) infection.
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spelling pubmed-104787362023-09-06 Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana Kim, Won-Jin Kim, Woong Kim, Youngsoon Cheong, Hyeonsook Kim, Seok-Jun Plant Signal Behav Research Paper Potato virus Y (PVY) is an aphid-transmitted potyvirus that affects economically important solanaceous species. In this study, the phenomena and mechanisms following infection with PVY were investigated in tobacco (Nicotiana benthamiana). In tobacco plants, infection with a mild strain of PVY (PVY(O)) induced stunted growth in the first two leaves at the shoot apex starting 7 days post-infection (dpi), and mosaic symptoms began to appear on newly developing young leaves at 14 dpi. Using enzyme-linked immunosorbent assay and ultrastructure analysis, we confirmed that viral particles accumulated only in the upper developing leaves of infected plants. We analyzed reactive oxygen species (ROS) generation in leaves from the bottom to the top of the plants to investigate whether delayed symptom development in leaves was associated with a defense response to the virus. In addition, the ultrastructural analysis confirmed the increase of ATG4 and ATG8, which are autophagy markers by endoplasmic reticulum (ER) stress, and the expression of genes involved in viral RNA suppression. Overall, our results suggested that viral RNA silencing and induced autophagy may play a role in the inhibition of viral symptom development in host plants in response to PVY(O) infection. Taylor & Francis 2023-09-01 /pmc/articles/PMC10478736/ /pubmed/37655790 http://dx.doi.org/10.1080/15592324.2023.2252972 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Paper
Kim, Won-Jin
Kim, Woong
Kim, Youngsoon
Cheong, Hyeonsook
Kim, Seok-Jun
Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana
title Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana
title_full Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana
title_fullStr Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana
title_full_unstemmed Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana
title_short Coordinated recruitment of conserved defense-signaling pathways in PVY(O)-Infected Nicotiana benthamiana
title_sort coordinated recruitment of conserved defense-signaling pathways in pvy(o)-infected nicotiana benthamiana
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478736/
https://www.ncbi.nlm.nih.gov/pubmed/37655790
http://dx.doi.org/10.1080/15592324.2023.2252972
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