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Efficient control of western flower thrips by plastid-mediated RNA interference

Plastid-mediated RNA interference (PM-RNAi) has emerged as a promising strategy for pest control. Expression from the plastid genome of stable double-stranded RNAs (dsRNAs) targeted against essential insect genes can effectively control some herbivorous beetles, but little is known about the efficac...

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Autores principales: Wu, Mengting, Dong, Yi, Zhang, Qi, Li, Shengchun, Chang, Ling, Loiacono, F. Vanessa, Ruf, Stephanie, Zhang, Jiang, Bock, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169809/
https://www.ncbi.nlm.nih.gov/pubmed/35380896
http://dx.doi.org/10.1073/pnas.2120081119
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author Wu, Mengting
Dong, Yi
Zhang, Qi
Li, Shengchun
Chang, Ling
Loiacono, F. Vanessa
Ruf, Stephanie
Zhang, Jiang
Bock, Ralph
author_facet Wu, Mengting
Dong, Yi
Zhang, Qi
Li, Shengchun
Chang, Ling
Loiacono, F. Vanessa
Ruf, Stephanie
Zhang, Jiang
Bock, Ralph
author_sort Wu, Mengting
collection PubMed
description Plastid-mediated RNA interference (PM-RNAi) has emerged as a promising strategy for pest control. Expression from the plastid genome of stable double-stranded RNAs (dsRNAs) targeted against essential insect genes can effectively control some herbivorous beetles, but little is known about the efficacy of the transplastomic approach in other groups of pest insects, especially nonchewing insects that do not consume large amounts of leaf material. Here we have investigated the susceptibility of the western flower thrip (WFT, Frankliniella occidentalis), a notorious pest in greenhouses and open fields, to PM-RNAi. We show that WFTs ingest chloroplasts and take up plastid-expressed dsRNAs. We generated a series of transplastomic tobacco plants expressing dsRNAs and hairpin RNAs (hpRNAs) targeted against four essential WFT genes. Unexpectedly, we discovered plastid genome instability in transplastomic plants expressing hpRNAs, suggesting that dsRNA cassettes are preferable over hpRNA cassettes when designing PM-RNAi strategies. Feeding studies revealed that, unlike nuclear transgenic plants, transplastomic plants induced a potent RNAi response in WFTs, causing efficient suppression of the targeted genes and high insect mortality. Our study extends the application range of PM-RNAi technology to an important group of nonchewing insects, reveals design principles for the construction of dsRNA-expressing transplastomic plants, and provides an efficient approach to control one of the toughest insect pests in agriculture and horticulture.
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spelling pubmed-91698092022-10-05 Efficient control of western flower thrips by plastid-mediated RNA interference Wu, Mengting Dong, Yi Zhang, Qi Li, Shengchun Chang, Ling Loiacono, F. Vanessa Ruf, Stephanie Zhang, Jiang Bock, Ralph Proc Natl Acad Sci U S A Biological Sciences Plastid-mediated RNA interference (PM-RNAi) has emerged as a promising strategy for pest control. Expression from the plastid genome of stable double-stranded RNAs (dsRNAs) targeted against essential insect genes can effectively control some herbivorous beetles, but little is known about the efficacy of the transplastomic approach in other groups of pest insects, especially nonchewing insects that do not consume large amounts of leaf material. Here we have investigated the susceptibility of the western flower thrip (WFT, Frankliniella occidentalis), a notorious pest in greenhouses and open fields, to PM-RNAi. We show that WFTs ingest chloroplasts and take up plastid-expressed dsRNAs. We generated a series of transplastomic tobacco plants expressing dsRNAs and hairpin RNAs (hpRNAs) targeted against four essential WFT genes. Unexpectedly, we discovered plastid genome instability in transplastomic plants expressing hpRNAs, suggesting that dsRNA cassettes are preferable over hpRNA cassettes when designing PM-RNAi strategies. Feeding studies revealed that, unlike nuclear transgenic plants, transplastomic plants induced a potent RNAi response in WFTs, causing efficient suppression of the targeted genes and high insect mortality. Our study extends the application range of PM-RNAi technology to an important group of nonchewing insects, reveals design principles for the construction of dsRNA-expressing transplastomic plants, and provides an efficient approach to control one of the toughest insect pests in agriculture and horticulture. National Academy of Sciences 2022-04-05 2022-04-12 /pmc/articles/PMC9169809/ /pubmed/35380896 http://dx.doi.org/10.1073/pnas.2120081119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Wu, Mengting
Dong, Yi
Zhang, Qi
Li, Shengchun
Chang, Ling
Loiacono, F. Vanessa
Ruf, Stephanie
Zhang, Jiang
Bock, Ralph
Efficient control of western flower thrips by plastid-mediated RNA interference
title Efficient control of western flower thrips by plastid-mediated RNA interference
title_full Efficient control of western flower thrips by plastid-mediated RNA interference
title_fullStr Efficient control of western flower thrips by plastid-mediated RNA interference
title_full_unstemmed Efficient control of western flower thrips by plastid-mediated RNA interference
title_short Efficient control of western flower thrips by plastid-mediated RNA interference
title_sort efficient control of western flower thrips by plastid-mediated rna interference
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169809/
https://www.ncbi.nlm.nih.gov/pubmed/35380896
http://dx.doi.org/10.1073/pnas.2120081119
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