Cargando…

Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali

Development of a reliable method for RNA interference (RNAi) by orally-delivered double-stranded RNA (dsRNA) is potentially promising for crop protection. Considering that RNAi efficiency considerably varies among different insect species, it is important to seek for the practical conditions under w...

Descripción completa

Detalles Bibliográficos
Autores principales: Nishide, Yudai, Kageyama, Daisuke, Tanaka, Yoshiaki, Yokoi, Kakeru, Jouraku, Akiya, Futahashi, Ryo, Fukatsu, Takema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808618/
https://www.ncbi.nlm.nih.gov/pubmed/33444324
http://dx.doi.org/10.1371/journal.pone.0245081
_version_ 1783636937848913920
author Nishide, Yudai
Kageyama, Daisuke
Tanaka, Yoshiaki
Yokoi, Kakeru
Jouraku, Akiya
Futahashi, Ryo
Fukatsu, Takema
author_facet Nishide, Yudai
Kageyama, Daisuke
Tanaka, Yoshiaki
Yokoi, Kakeru
Jouraku, Akiya
Futahashi, Ryo
Fukatsu, Takema
author_sort Nishide, Yudai
collection PubMed
description Development of a reliable method for RNA interference (RNAi) by orally-delivered double-stranded RNA (dsRNA) is potentially promising for crop protection. Considering that RNAi efficiency considerably varies among different insect species, it is important to seek for the practical conditions under which dsRNA-mediated RNAi effectively works against each pest insect. Here we investigated RNAi efficiency in the brown-winged green stinkbug Plautia stali, which is notorious for infesting various fruits and crop plants. Microinjection of dsRNA into P. stali revealed high RNAi efficiency–injection of only 30 ng dsRNA into last-instar nymphs was sufficient to knockdown target genes as manifested by their phenotypes, and injection of 300 ng dsRNA suppressed the gene expression levels by 80% to 99.9%. Knockdown experiments by dsRNA injection showed that multicopper oxidase 2 (MCO2), vacuolar ATPase (vATPase), inhibitor of apoptosis (IAP), and vacuolar-sorting protein Snf7 are essential for survival of P. stali, as has been demonstrated in other insects. By contrast, P. stali exhibited very low RNAi efficiency when dsRNA was orally administered. When 1000 ng/μL of dsRNA solution was orally provided to first-instar nymphs, no obvious phenotypes were observed. Consistent with this, RT-qPCR showed that the gene expression levels were not affected. A higher concentration of dsRNA (5000 ng/μL) induced mortality in some cohorts, and the gene expression levels were reduced to nearly 50%. Simultaneous oral administration of dsRNA against potential RNAi blocker genes did not improve the RNAi efficiency of the target genes. In conclusion, P. stali shows high sensitivity to RNAi with injected dsRNA but, unlike the allied pest stinkbugs Halyomorpha halys and Nezara viridula, very low sensitivity to RNAi with orally-delivered dsRNA, which highlights the varied sensitivity to RNAi across different species and limits the applicability of the molecular tool for controlling this specific insect pest.
format Online
Article
Text
id pubmed-7808618
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-78086182021-02-02 Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali Nishide, Yudai Kageyama, Daisuke Tanaka, Yoshiaki Yokoi, Kakeru Jouraku, Akiya Futahashi, Ryo Fukatsu, Takema PLoS One Research Article Development of a reliable method for RNA interference (RNAi) by orally-delivered double-stranded RNA (dsRNA) is potentially promising for crop protection. Considering that RNAi efficiency considerably varies among different insect species, it is important to seek for the practical conditions under which dsRNA-mediated RNAi effectively works against each pest insect. Here we investigated RNAi efficiency in the brown-winged green stinkbug Plautia stali, which is notorious for infesting various fruits and crop plants. Microinjection of dsRNA into P. stali revealed high RNAi efficiency–injection of only 30 ng dsRNA into last-instar nymphs was sufficient to knockdown target genes as manifested by their phenotypes, and injection of 300 ng dsRNA suppressed the gene expression levels by 80% to 99.9%. Knockdown experiments by dsRNA injection showed that multicopper oxidase 2 (MCO2), vacuolar ATPase (vATPase), inhibitor of apoptosis (IAP), and vacuolar-sorting protein Snf7 are essential for survival of P. stali, as has been demonstrated in other insects. By contrast, P. stali exhibited very low RNAi efficiency when dsRNA was orally administered. When 1000 ng/μL of dsRNA solution was orally provided to first-instar nymphs, no obvious phenotypes were observed. Consistent with this, RT-qPCR showed that the gene expression levels were not affected. A higher concentration of dsRNA (5000 ng/μL) induced mortality in some cohorts, and the gene expression levels were reduced to nearly 50%. Simultaneous oral administration of dsRNA against potential RNAi blocker genes did not improve the RNAi efficiency of the target genes. In conclusion, P. stali shows high sensitivity to RNAi with injected dsRNA but, unlike the allied pest stinkbugs Halyomorpha halys and Nezara viridula, very low sensitivity to RNAi with orally-delivered dsRNA, which highlights the varied sensitivity to RNAi across different species and limits the applicability of the molecular tool for controlling this specific insect pest. Public Library of Science 2021-01-14 /pmc/articles/PMC7808618/ /pubmed/33444324 http://dx.doi.org/10.1371/journal.pone.0245081 Text en © 2021 Nishide et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nishide, Yudai
Kageyama, Daisuke
Tanaka, Yoshiaki
Yokoi, Kakeru
Jouraku, Akiya
Futahashi, Ryo
Fukatsu, Takema
Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali
title Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali
title_full Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali
title_fullStr Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali
title_full_unstemmed Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali
title_short Effectiveness of orally-delivered double-stranded RNA on gene silencing in the stinkbug Plautia stali
title_sort effectiveness of orally-delivered double-stranded rna on gene silencing in the stinkbug plautia stali
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808618/
https://www.ncbi.nlm.nih.gov/pubmed/33444324
http://dx.doi.org/10.1371/journal.pone.0245081
work_keys_str_mv AT nishideyudai effectivenessoforallydelivereddoublestrandedrnaongenesilencinginthestinkbugplautiastali
AT kageyamadaisuke effectivenessoforallydelivereddoublestrandedrnaongenesilencinginthestinkbugplautiastali
AT tanakayoshiaki effectivenessoforallydelivereddoublestrandedrnaongenesilencinginthestinkbugplautiastali
AT yokoikakeru effectivenessoforallydelivereddoublestrandedrnaongenesilencinginthestinkbugplautiastali
AT jourakuakiya effectivenessoforallydelivereddoublestrandedrnaongenesilencinginthestinkbugplautiastali
AT futahashiryo effectivenessoforallydelivereddoublestrandedrnaongenesilencinginthestinkbugplautiastali
AT fukatsutakema effectivenessoforallydelivereddoublestrandedrnaongenesilencinginthestinkbugplautiastali