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Cocksfoot mottle virus coat protein is dispensable for the systemic infection
BACKGROUND: The Sobemovirus genome consists of polycistronic single-stranded positive-sense RNA. The first ORF encodes P1, a suppressor of RNA silencing required for virus movement. The coat protein (CP) is expressed from the 3′ proximal ORF3 via subgenomic RNA. In addition to its structural role, t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925361/ https://www.ncbi.nlm.nih.gov/pubmed/24495467 http://dx.doi.org/10.1186/1743-422X-11-19 |
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author | Olspert, Allan Kamsol, Kristjan Sarmiento, Cecilia Gerassimenko, Jelena Truve, Erkki |
author_facet | Olspert, Allan Kamsol, Kristjan Sarmiento, Cecilia Gerassimenko, Jelena Truve, Erkki |
author_sort | Olspert, Allan |
collection | PubMed |
description | BACKGROUND: The Sobemovirus genome consists of polycistronic single-stranded positive-sense RNA. The first ORF encodes P1, a suppressor of RNA silencing required for virus movement. The coat protein (CP) is expressed from the 3′ proximal ORF3 via subgenomic RNA. In addition to its structural role, the CP of some sobemoviruses has been reported to be required for systemic movement and to interact with P1. The aim of this study was to analyse the role of Cocksfoot mottle virus (CfMV) CP in the suppression of RNA silencing and virus movement. METHODS: Agrobacterium-mediated transient expression method was used for testing CfMV CP capacity to suppress RNA silencing. CP substitution and deletion mutants were generated to examine the role of this protein in CfMV infection, using three host plants (oat, barley and wheat). The viral movement was characterised with CfMV expressing EGFP fused to the C-terminus of CP. RESULTS: In the current study we show that CfMV CP is an additional RNA silencing suppressor. Interestingly, we observed that all CP mutant viruses were able to infect the three tested host plants systemically, although usually with reduced accumulation. CfMV expressing EGFP was detected in epidermal and mesophyll cells of inoculated leaves. Although EGFP fluorescence was not detected in upper leaves, some plants displayed CfMV symptoms. Analysis of the upper leaves revealed that the viruses had lost the EGFP sequence and sometimes also most of the CP gene. CONCLUSIONS: The present study demonstrates that CfMV CP suppresses RNA silencing but, surprisingly, is dispensable for systemic movement. Thus, CfMV does not move as virion in the tested host plants. The composition of the movement RNP complex remains to be elucidated. |
format | Online Article Text |
id | pubmed-3925361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39253612014-02-16 Cocksfoot mottle virus coat protein is dispensable for the systemic infection Olspert, Allan Kamsol, Kristjan Sarmiento, Cecilia Gerassimenko, Jelena Truve, Erkki Virol J Research BACKGROUND: The Sobemovirus genome consists of polycistronic single-stranded positive-sense RNA. The first ORF encodes P1, a suppressor of RNA silencing required for virus movement. The coat protein (CP) is expressed from the 3′ proximal ORF3 via subgenomic RNA. In addition to its structural role, the CP of some sobemoviruses has been reported to be required for systemic movement and to interact with P1. The aim of this study was to analyse the role of Cocksfoot mottle virus (CfMV) CP in the suppression of RNA silencing and virus movement. METHODS: Agrobacterium-mediated transient expression method was used for testing CfMV CP capacity to suppress RNA silencing. CP substitution and deletion mutants were generated to examine the role of this protein in CfMV infection, using three host plants (oat, barley and wheat). The viral movement was characterised with CfMV expressing EGFP fused to the C-terminus of CP. RESULTS: In the current study we show that CfMV CP is an additional RNA silencing suppressor. Interestingly, we observed that all CP mutant viruses were able to infect the three tested host plants systemically, although usually with reduced accumulation. CfMV expressing EGFP was detected in epidermal and mesophyll cells of inoculated leaves. Although EGFP fluorescence was not detected in upper leaves, some plants displayed CfMV symptoms. Analysis of the upper leaves revealed that the viruses had lost the EGFP sequence and sometimes also most of the CP gene. CONCLUSIONS: The present study demonstrates that CfMV CP suppresses RNA silencing but, surprisingly, is dispensable for systemic movement. Thus, CfMV does not move as virion in the tested host plants. The composition of the movement RNP complex remains to be elucidated. BioMed Central 2014-02-04 /pmc/articles/PMC3925361/ /pubmed/24495467 http://dx.doi.org/10.1186/1743-422X-11-19 Text en Copyright © 2014 Olspert et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Olspert, Allan Kamsol, Kristjan Sarmiento, Cecilia Gerassimenko, Jelena Truve, Erkki Cocksfoot mottle virus coat protein is dispensable for the systemic infection |
title | Cocksfoot mottle virus coat protein is dispensable for the systemic infection |
title_full | Cocksfoot mottle virus coat protein is dispensable for the systemic infection |
title_fullStr | Cocksfoot mottle virus coat protein is dispensable for the systemic infection |
title_full_unstemmed | Cocksfoot mottle virus coat protein is dispensable for the systemic infection |
title_short | Cocksfoot mottle virus coat protein is dispensable for the systemic infection |
title_sort | cocksfoot mottle virus coat protein is dispensable for the systemic infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925361/ https://www.ncbi.nlm.nih.gov/pubmed/24495467 http://dx.doi.org/10.1186/1743-422X-11-19 |
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