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Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera

The polyphagous insect-pest, Helicoverpa armigera, is a serious threat to a number of economically important crops. Chemical application and/or cultivation of Bt transgenic crops are the two strategies available now for insect-pest management. However, environmental pollution and long-term sustainab...

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Autores principales: Saini, Ravi Prakash, Raman, Venkat, Dhandapani, Gurusamy, Malhotra, Era Vaidya, Sreevathsa, Rohini, Kumar, Polumetla Ananda, Sharma, Tilak R., Pattanayak, Debasis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856398/
https://www.ncbi.nlm.nih.gov/pubmed/29547640
http://dx.doi.org/10.1371/journal.pone.0194150
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author Saini, Ravi Prakash
Raman, Venkat
Dhandapani, Gurusamy
Malhotra, Era Vaidya
Sreevathsa, Rohini
Kumar, Polumetla Ananda
Sharma, Tilak R.
Pattanayak, Debasis
author_facet Saini, Ravi Prakash
Raman, Venkat
Dhandapani, Gurusamy
Malhotra, Era Vaidya
Sreevathsa, Rohini
Kumar, Polumetla Ananda
Sharma, Tilak R.
Pattanayak, Debasis
author_sort Saini, Ravi Prakash
collection PubMed
description The polyphagous insect-pest, Helicoverpa armigera, is a serious threat to a number of economically important crops. Chemical application and/or cultivation of Bt transgenic crops are the two strategies available now for insect-pest management. However, environmental pollution and long-term sustainability are major concerns against these two options. RNAi is now considered as a promising technology to complement Bt to tackle insect-pests menace. In this study, we report host-delivered silencing of HaAce1 gene, encoding the predominant isoform of H. armigera acetylcholinesterase, by an artificial microRNA, HaAce1-amiR1. Arabidopsis pre-miRNA164b was modified by replacing miR164b/miR164b* sequences with HaAce1-amiR1/HaAce1-amiR1* sequences. The recombinant HaAce1-preamiRNA1 was put under the control of CaMV 35S promoter and NOS terminator of plant binary vector pBI121, and the resultant vector cassette was used for tobacco transformation. Two transgenic tobacco lines expressing HaAce1-amiR1 was used for detached leaf insect feeding bioassays. Larval mortality of 25% and adult deformity of 20% were observed in transgenic treated insect group over that control tobacco treated insect group. The reduction in the steady-state level of HaAce1 mRNA was 70–80% in the defective adults compared to control. Our results demonstrate promise for host-delivered amiRNA-mediated silencing of HaAce1 gene for H. armigera management.
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spelling pubmed-58563982018-03-28 Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera Saini, Ravi Prakash Raman, Venkat Dhandapani, Gurusamy Malhotra, Era Vaidya Sreevathsa, Rohini Kumar, Polumetla Ananda Sharma, Tilak R. Pattanayak, Debasis PLoS One Research Article The polyphagous insect-pest, Helicoverpa armigera, is a serious threat to a number of economically important crops. Chemical application and/or cultivation of Bt transgenic crops are the two strategies available now for insect-pest management. However, environmental pollution and long-term sustainability are major concerns against these two options. RNAi is now considered as a promising technology to complement Bt to tackle insect-pests menace. In this study, we report host-delivered silencing of HaAce1 gene, encoding the predominant isoform of H. armigera acetylcholinesterase, by an artificial microRNA, HaAce1-amiR1. Arabidopsis pre-miRNA164b was modified by replacing miR164b/miR164b* sequences with HaAce1-amiR1/HaAce1-amiR1* sequences. The recombinant HaAce1-preamiRNA1 was put under the control of CaMV 35S promoter and NOS terminator of plant binary vector pBI121, and the resultant vector cassette was used for tobacco transformation. Two transgenic tobacco lines expressing HaAce1-amiR1 was used for detached leaf insect feeding bioassays. Larval mortality of 25% and adult deformity of 20% were observed in transgenic treated insect group over that control tobacco treated insect group. The reduction in the steady-state level of HaAce1 mRNA was 70–80% in the defective adults compared to control. Our results demonstrate promise for host-delivered amiRNA-mediated silencing of HaAce1 gene for H. armigera management. Public Library of Science 2018-03-16 /pmc/articles/PMC5856398/ /pubmed/29547640 http://dx.doi.org/10.1371/journal.pone.0194150 Text en © 2018 Saini 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
Saini, Ravi Prakash
Raman, Venkat
Dhandapani, Gurusamy
Malhotra, Era Vaidya
Sreevathsa, Rohini
Kumar, Polumetla Ananda
Sharma, Tilak R.
Pattanayak, Debasis
Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera
title Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera
title_full Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera
title_fullStr Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera
title_full_unstemmed Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera
title_short Silencing of HaAce1 gene by host-delivered artificial microRNA disrupts growth and development of Helicoverpa armigera
title_sort silencing of haace1 gene by host-delivered artificial microrna disrupts growth and development of helicoverpa armigera
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856398/
https://www.ncbi.nlm.nih.gov/pubmed/29547640
http://dx.doi.org/10.1371/journal.pone.0194150
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