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Development of RNAi methods to control the harlequin bug, Murgantia histrionica

Producción científica: Articlerevisión exhaustiva

16 Citas (Scopus)

Resumen

The harlequin bug (HB), Murgantia histrionica, is a major pest of cabbage family plants throughout its range in the United States. RNA interference (RNAi) is a posttranscriptional gene silencing mechanism that is showing promise as a biopesticide due to the ability to target species-specific genes necessary for growth and/or survival with synthetic double-stranded RNA (dsRNA). In the present study, dsRNA stability assays revealed that nucleases present in the saliva of harlequin bugs did not rapidly degrade dsRNA. We tracked the movement and localization of radioactively labeled dsRNA in both mustard plant seedlings and harlequin bug nymphs that fed on treated host plants. Movement of 32P-labeled-dsRNA from soil to plant and plant to insect was detected. The efficacy of RNAi in inducing mortality in harlequin bug adults and nymphs injected or fed with dsRNA targeting inhibitor of apoptosis (IAP), ATPase N2B (ATPase), serine/threonine-protein phosphatase PP1-β catalytic subunit (PP1), signal recognition particle 54 kDa protein (SRP), and G protein-coupled receptor 161-like (GPCR) genes was evaluated. Injection of dsRNA targeting candidate genes into adults caused between 40% and 75% mortality and induced significant knockdown of target gene expression. Feeding dsRNA targeting the IAP gene to nymphs by plant-mediated and droplet feeding methods induced knockdown of the target gene and caused 40–55% mortality. These findings suggest that RNAi may be a viable approach for managing this pest.

Idioma originalEnglish
Número de artículoe21690
PublicaciónArchives of Insect Biochemistry and Physiology
Volumen104
N.º4
DOI
EstadoPublished - ago 1 2020

Nota bibliográfica

Publisher Copyright:
© 2020 Wiley Periodicals LLC

Financiación

This study was supported by grants from the National Institutes of Health (GM070559‐14 and 1R21AI131427‐01), the National Science Foundation (Industry/University Cooperative Research Centers, the Center for Arthropod Management Technologies under Grant IIP‐1821936), Agriculture and Food Research Initiative Competitive grant no. 2019‐67013‐29351, and the National Institute of Food and Agriculture, US Department of Agriculture (under HATCH Project 2353057000). This study was supported by grants from the National Institutes of Health (GM070559-14 and 1R21AI131427-01), the National Science Foundation (Industry/University Cooperative Research Centers, the Center for Arthropod Management Technologies under Grant IIP-1821936), Agriculture and Food Research Initiative Competitive grant no. 2019-67013-29351, and the National Institute of Food and Agriculture, US Department of Agriculture (under HATCH Project 2353057000).

FinanciadoresNúmero del financiador
Center for Arthropod Management Technologies
US Department of Agriculture
National Science Foundation Arctic Social Science Program
National Institutes of Health (NIH)1R21AI131427‐01, GM070559‐14
National Institutes of Health (NIH)
U.S. Department of Agriculture2353057000
U.S. Department of Agriculture
US Department of Agriculture National Institute of Food and Agriculture, Agriculture and Food Research Initiative
Center for Arthropod Management TechnologiesIIP‐1821936, 2019‐67013‐29351
Center for Arthropod Management Technologies

    ASJC Scopus subject areas

    • Physiology
    • Biochemistry
    • Insect Science

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