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Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans
RNA interference (RNAi) is a sequence identity-dependent RNA degradation mechanism conserved in eukaryotic organisms. One of the roles of RNAi is as a defense system against viral infections, which has been demonstrated in filamentous fungi but not in oomycetes. We investigated the virus-RNAi interp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390105/ https://www.ncbi.nlm.nih.gov/pubmed/30804453 http://dx.doi.org/10.1038/s41598-019-39162-w |
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author | Mascia, Tiziana Labarile, Rossella Doohan, Fiona Gallitelli, Donato |
author_facet | Mascia, Tiziana Labarile, Rossella Doohan, Fiona Gallitelli, Donato |
author_sort | Mascia, Tiziana |
collection | PubMed |
description | RNA interference (RNAi) is a sequence identity-dependent RNA degradation mechanism conserved in eukaryotic organisms. One of the roles of RNAi is as a defense system against viral infections, which has been demonstrated in filamentous fungi but not in oomycetes. We investigated the virus-RNAi interplay in the oomycete Phytophthora infestans using a crucifer-infecting strain of the plant virus tobacco mosaic virus (TMVcr) and its derivative TMVcr-Δ122 that is mutated in the sequence of the p122 replicase subunit and thus inhibited in RNA suppression activity. In this study we provide evidence that replication of TMVcr-Δ122 but not of TMVcr was impaired in P. infestans as well as in tobacco plants used as positive control. The interference was associated with induction of high transcription of dicer-like genes Pidcl2 and NtDCL2 and of RNA-dependent-RNA-polymerase Pirdr1 and NtRDR1 in P. infestans and tobacco, respectively. These high transcription levels suggest an RNAi-based response that TMVcr-Δ122 mutant was not able to suppress. Taken altogether, results of this study demonstrated that an antiviral silencing activity operates also in P. infestans and that a plant virus could be a simple and feasible tool for functional studies also in oomycetes. |
format | Online Article Text |
id | pubmed-6390105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63901052019-02-28 Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans Mascia, Tiziana Labarile, Rossella Doohan, Fiona Gallitelli, Donato Sci Rep Article RNA interference (RNAi) is a sequence identity-dependent RNA degradation mechanism conserved in eukaryotic organisms. One of the roles of RNAi is as a defense system against viral infections, which has been demonstrated in filamentous fungi but not in oomycetes. We investigated the virus-RNAi interplay in the oomycete Phytophthora infestans using a crucifer-infecting strain of the plant virus tobacco mosaic virus (TMVcr) and its derivative TMVcr-Δ122 that is mutated in the sequence of the p122 replicase subunit and thus inhibited in RNA suppression activity. In this study we provide evidence that replication of TMVcr-Δ122 but not of TMVcr was impaired in P. infestans as well as in tobacco plants used as positive control. The interference was associated with induction of high transcription of dicer-like genes Pidcl2 and NtDCL2 and of RNA-dependent-RNA-polymerase Pirdr1 and NtRDR1 in P. infestans and tobacco, respectively. These high transcription levels suggest an RNAi-based response that TMVcr-Δ122 mutant was not able to suppress. Taken altogether, results of this study demonstrated that an antiviral silencing activity operates also in P. infestans and that a plant virus could be a simple and feasible tool for functional studies also in oomycetes. Nature Publishing Group UK 2019-02-25 /pmc/articles/PMC6390105/ /pubmed/30804453 http://dx.doi.org/10.1038/s41598-019-39162-w Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mascia, Tiziana Labarile, Rossella Doohan, Fiona Gallitelli, Donato Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans |
title | Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans |
title_full | Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans |
title_fullStr | Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans |
title_full_unstemmed | Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans |
title_short | Tobacco mosaic virus infection triggers an RNAi-based response in Phytophthora infestans |
title_sort | tobacco mosaic virus infection triggers an rnai-based response in phytophthora infestans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390105/ https://www.ncbi.nlm.nih.gov/pubmed/30804453 http://dx.doi.org/10.1038/s41598-019-39162-w |
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