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Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana
The sugarcane streak mosaic virus (SCSMV) is the most important disease in sugarcane produced in southern China. The SCSMV encoded protein 1 (P1(SCSMV)) is important in disease development, but little is known about its detailed functions in plant–virus interactions. Here, the differential accumulat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497147/ https://www.ncbi.nlm.nih.gov/pubmed/36139443 http://dx.doi.org/10.3390/cells11182870 |
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author | Zhang, Kun Xu, Xiaowei Guo, Xiao Ding, Shiwen Gu, Tianxiao Qin, Lang He, Zhen |
author_facet | Zhang, Kun Xu, Xiaowei Guo, Xiao Ding, Shiwen Gu, Tianxiao Qin, Lang He, Zhen |
author_sort | Zhang, Kun |
collection | PubMed |
description | The sugarcane streak mosaic virus (SCSMV) is the most important disease in sugarcane produced in southern China. The SCSMV encoded protein 1 (P1(SCSMV)) is important in disease development, but little is known about its detailed functions in plant–virus interactions. Here, the differential accumulated proteins (DAPs) were identified in the heterologous expression of P1(SCSMV) via a potato virus X (PVX)-based expression system, using a newly developed four-dimensional proteomics approach. The data were evaluated for credibility and reliability using qRT-RCR and Western blot analyses. The physiological response caused by host factors that directly interacted with the PVX-encoded proteins was more pronounced for enhancing the PVX accumulation and pathogenesis in Nicotiana benthamiana. P1(SCSMV) reduced photosynthesis by damaging the photosystem II (PSII). Overall, P1(SCSMV) promotes changes in the physiological status of its host by up- or downregulating the expression of host factors that directly interact with the viral proteins. This creates optimal conditions for PVX replication and movement, thereby enhancing its accumulation levels and pathogenesis. Our investigation is the first to supply detailed evidence of the pathogenesis-enhancing role of P1(SCSMV), which provides a deeper understanding of the mechanisms behind virus–host interactions. |
format | Online Article Text |
id | pubmed-9497147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94971472022-09-23 Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana Zhang, Kun Xu, Xiaowei Guo, Xiao Ding, Shiwen Gu, Tianxiao Qin, Lang He, Zhen Cells Article The sugarcane streak mosaic virus (SCSMV) is the most important disease in sugarcane produced in southern China. The SCSMV encoded protein 1 (P1(SCSMV)) is important in disease development, but little is known about its detailed functions in plant–virus interactions. Here, the differential accumulated proteins (DAPs) were identified in the heterologous expression of P1(SCSMV) via a potato virus X (PVX)-based expression system, using a newly developed four-dimensional proteomics approach. The data were evaluated for credibility and reliability using qRT-RCR and Western blot analyses. The physiological response caused by host factors that directly interacted with the PVX-encoded proteins was more pronounced for enhancing the PVX accumulation and pathogenesis in Nicotiana benthamiana. P1(SCSMV) reduced photosynthesis by damaging the photosystem II (PSII). Overall, P1(SCSMV) promotes changes in the physiological status of its host by up- or downregulating the expression of host factors that directly interact with the viral proteins. This creates optimal conditions for PVX replication and movement, thereby enhancing its accumulation levels and pathogenesis. Our investigation is the first to supply detailed evidence of the pathogenesis-enhancing role of P1(SCSMV), which provides a deeper understanding of the mechanisms behind virus–host interactions. MDPI 2022-09-14 /pmc/articles/PMC9497147/ /pubmed/36139443 http://dx.doi.org/10.3390/cells11182870 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Kun Xu, Xiaowei Guo, Xiao Ding, Shiwen Gu, Tianxiao Qin, Lang He, Zhen Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana |
title | Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana |
title_full | Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana |
title_fullStr | Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana |
title_full_unstemmed | Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana |
title_short | Sugarcane Streak Mosaic Virus P1 Attenuates Plant Antiviral Immunity and Enhances Potato Virus X Infection in Nicotiana benthamiana |
title_sort | sugarcane streak mosaic virus p1 attenuates plant antiviral immunity and enhances potato virus x infection in nicotiana benthamiana |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497147/ https://www.ncbi.nlm.nih.gov/pubmed/36139443 http://dx.doi.org/10.3390/cells11182870 |
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