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Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection
Aggressive fungal pathogens such as Botrytis and Verticillium spp. cause severe crop losses worldwide. We recently discovered that Botrytis cinerea delivers small RNAs (Bc-sRNAs) into plant cells to silence host immunity genes. Such sRNA effectors are mostly produced by B. cinerea Dicer-like protein...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040644/ https://www.ncbi.nlm.nih.gov/pubmed/27643635 http://dx.doi.org/10.1038/nplants.2016.151 |
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author | Wang, Ming Weiberg, Arne Lin, Feng-Mao Thomma, Bart Huang, Hsien-Da Jin, Hailing |
author_facet | Wang, Ming Weiberg, Arne Lin, Feng-Mao Thomma, Bart Huang, Hsien-Da Jin, Hailing |
author_sort | Wang, Ming |
collection | PubMed |
description | Aggressive fungal pathogens such as Botrytis and Verticillium spp. cause severe crop losses worldwide. We recently discovered that Botrytis cinerea delivers small RNAs (Bc-sRNAs) into plant cells to silence host immunity genes. Such sRNA effectors are mostly produced by B. cinerea Dicer-like protein 1 (Bc-DCL1) and Bc-DCL2. Here we show that expressing sRNAs that target Bc-DCL1 and Bc-DCL2 in Arabidopsis and tomato silences Bc-DCL genes and attenuates fungal pathogenicity and growth, exemplifying bidirectional cross-kingdom RNAi and sRNA trafficking between plants and fungi. This strategy can be adapted to simultaneously control multiple fungal diseases. We also show that Botrytis can take up external sRNAs and double-stranded RNAs (dsRNAs). Applying sRNAs or dsRNAs that target Botrytis DCL1 and DCL2 genes on the surface of fruits, vegetables, and flowers significantly inhibits gray mold disease. Such pathogen gene-targeting RNAs represent a new generation of environmentally-friendly fungicides. |
format | Online Article Text |
id | pubmed-5040644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-50406442017-03-19 Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection Wang, Ming Weiberg, Arne Lin, Feng-Mao Thomma, Bart Huang, Hsien-Da Jin, Hailing Nat Plants Article Aggressive fungal pathogens such as Botrytis and Verticillium spp. cause severe crop losses worldwide. We recently discovered that Botrytis cinerea delivers small RNAs (Bc-sRNAs) into plant cells to silence host immunity genes. Such sRNA effectors are mostly produced by B. cinerea Dicer-like protein 1 (Bc-DCL1) and Bc-DCL2. Here we show that expressing sRNAs that target Bc-DCL1 and Bc-DCL2 in Arabidopsis and tomato silences Bc-DCL genes and attenuates fungal pathogenicity and growth, exemplifying bidirectional cross-kingdom RNAi and sRNA trafficking between plants and fungi. This strategy can be adapted to simultaneously control multiple fungal diseases. We also show that Botrytis can take up external sRNAs and double-stranded RNAs (dsRNAs). Applying sRNAs or dsRNAs that target Botrytis DCL1 and DCL2 genes on the surface of fruits, vegetables, and flowers significantly inhibits gray mold disease. Such pathogen gene-targeting RNAs represent a new generation of environmentally-friendly fungicides. 2016-09-19 /pmc/articles/PMC5040644/ /pubmed/27643635 http://dx.doi.org/10.1038/nplants.2016.151 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Wang, Ming Weiberg, Arne Lin, Feng-Mao Thomma, Bart Huang, Hsien-Da Jin, Hailing Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection |
title | Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection |
title_full | Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection |
title_fullStr | Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection |
title_full_unstemmed | Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection |
title_short | Bidirectional cross-kingdom RNAi and fungal uptake of external RNAs confer plant protection |
title_sort | bidirectional cross-kingdom rnai and fungal uptake of external rnas confer plant protection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040644/ https://www.ncbi.nlm.nih.gov/pubmed/27643635 http://dx.doi.org/10.1038/nplants.2016.151 |
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