Cargando…
Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species
The slow lethality of fungal biopesticides to insects restrains their widespread application as a strategy of pest control. In this study, unary, binary and ternary transgenic Metarhizium robertsii were created by integrating genes that encode the scorpion neurotoxin BjαIT, the cuticle‐degrading pro...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313288/ https://www.ncbi.nlm.nih.gov/pubmed/33459518 http://dx.doi.org/10.1111/1751-7915.13748 |
_version_ | 1783729313875492864 |
---|---|
author | Wang, Yulong Xie, Xiangyun Qin, Li Yu, Deshui Wang, Zhangxun Huang, Bo |
author_facet | Wang, Yulong Xie, Xiangyun Qin, Li Yu, Deshui Wang, Zhangxun Huang, Bo |
author_sort | Wang, Yulong |
collection | PubMed |
description | The slow lethality of fungal biopesticides to insects restrains their widespread application as a strategy of pest control. In this study, unary, binary and ternary transgenic Metarhizium robertsii were created by integrating genes that encode the scorpion neurotoxin BjαIT, the cuticle‐degrading protease Pr1A, and a double‐stranded RNA (dsRNA) that targets host gnbp3, individually or collectively under a constitutive promoter to enhance virulence. Compared with the parental wild type, all unary transgenic strains had increased virulence against four insect species, Tenebrio molitor, Locusta migratoria, Plutella xylostella and Galleria mellonella, whereas the binary transgenic strain expressing both pr1A and BjαIT had increased virulence to T. molitor and L. migratoria, with no change in virulence against P. xylostella and G. mellonella. Importantly, all ternary transgenic strains simultaneously expressing pr1A, BjαIT, and the dsRNA specific to host gnbp3 exhibited the highest increase in insect‐specific virulence. This finding highlights a novel strategy for genetic engineering of dsRNAs that target genes associated with the host immune response alongside virulence genes to maximize fungal virulence and lethality against insect pests. |
format | Online Article Text |
id | pubmed-8313288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83132882021-07-30 Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species Wang, Yulong Xie, Xiangyun Qin, Li Yu, Deshui Wang, Zhangxun Huang, Bo Microb Biotechnol Research Articles The slow lethality of fungal biopesticides to insects restrains their widespread application as a strategy of pest control. In this study, unary, binary and ternary transgenic Metarhizium robertsii were created by integrating genes that encode the scorpion neurotoxin BjαIT, the cuticle‐degrading protease Pr1A, and a double‐stranded RNA (dsRNA) that targets host gnbp3, individually or collectively under a constitutive promoter to enhance virulence. Compared with the parental wild type, all unary transgenic strains had increased virulence against four insect species, Tenebrio molitor, Locusta migratoria, Plutella xylostella and Galleria mellonella, whereas the binary transgenic strain expressing both pr1A and BjαIT had increased virulence to T. molitor and L. migratoria, with no change in virulence against P. xylostella and G. mellonella. Importantly, all ternary transgenic strains simultaneously expressing pr1A, BjαIT, and the dsRNA specific to host gnbp3 exhibited the highest increase in insect‐specific virulence. This finding highlights a novel strategy for genetic engineering of dsRNAs that target genes associated with the host immune response alongside virulence genes to maximize fungal virulence and lethality against insect pests. John Wiley and Sons Inc. 2021-01-18 /pmc/articles/PMC8313288/ /pubmed/33459518 http://dx.doi.org/10.1111/1751-7915.13748 Text en © 2021 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Wang, Yulong Xie, Xiangyun Qin, Li Yu, Deshui Wang, Zhangxun Huang, Bo Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species |
title | Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species |
title_full | Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species |
title_fullStr | Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species |
title_full_unstemmed | Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species |
title_short | Integration of dsRNA against host immune response genes augments the virulence of transgenic Metarhizium robertsii strains in insect pest species |
title_sort | integration of dsrna against host immune response genes augments the virulence of transgenic metarhizium robertsii strains in insect pest species |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313288/ https://www.ncbi.nlm.nih.gov/pubmed/33459518 http://dx.doi.org/10.1111/1751-7915.13748 |
work_keys_str_mv | AT wangyulong integrationofdsrnaagainsthostimmuneresponsegenesaugmentsthevirulenceoftransgenicmetarhiziumrobertsiistrainsininsectpestspecies AT xiexiangyun integrationofdsrnaagainsthostimmuneresponsegenesaugmentsthevirulenceoftransgenicmetarhiziumrobertsiistrainsininsectpestspecies AT qinli integrationofdsrnaagainsthostimmuneresponsegenesaugmentsthevirulenceoftransgenicmetarhiziumrobertsiistrainsininsectpestspecies AT yudeshui integrationofdsrnaagainsthostimmuneresponsegenesaugmentsthevirulenceoftransgenicmetarhiziumrobertsiistrainsininsectpestspecies AT wangzhangxun integrationofdsrnaagainsthostimmuneresponsegenesaugmentsthevirulenceoftransgenicmetarhiziumrobertsiistrainsininsectpestspecies AT huangbo integrationofdsrnaagainsthostimmuneresponsegenesaugmentsthevirulenceoftransgenicmetarhiziumrobertsiistrainsininsectpestspecies |