Fluorescent Nanoparticle-RNAi-Mediated Silencing of Sterol Carrier Protein-2 Gene Expression Suppresses the Growth, Development, and Reproduction of Helicoverpa armigera .
Kexin GengYing ZhangXi ZhaoWanlin ZhangXinhan GuoLu HeKaiyu LiuHong YangHuazhu HongJianxin PengRong PengPublished in: Nanomaterials (Basel, Switzerland) (2023)
Helicoverpa armigera is a polyphagous destructive lepidopteran pest with strong Bacillus thuringiensis (Bt) resistance. Cholesterol, a vital component for insect growth, can only be obtained from food, and its transfer and metabolism are regulated by sterol carrier protein-2 (SCP-2). This study examined whether H. armigera SCP-2 ( HaSCP-2 ) gene expression, involved in cholesterol absorption, can be silenced by nanocarrier fluorescent nanoparticle-RNA interference (FNP-RNAi) by larval feeding and whether the silencing affected H. armigera development. Fluorescence microscopy showed that nanoparticle-siRNA was distributed in Ha cells and the larval midgut. FNP- HaSCP-2 siRNA suppressed HaSCP-2 expression by 52.5% in H.armigera Ha cells. FNP can effectively help deliver siRNA into cells, protect siRNA, and is not affected by serum. FNP-siRNA in vivo biological assays showed that HaSCP-2 transcript levels were inhibited by 70.19%, 68.16%, and 67.66% in 3rd, 4th, and 5th instar larvae, leading to a decrease in the cholesterol level in the larval and prepupal fatbodies. The pupation rate and adult emergence were reduced to 26.0% and 56.52%, respectively. This study demonstrated that FNP could deliver siRNA to cells and improve siRNA knockdown efficiency. HaSCP-2 knockdown by FNP-siRNA in vivo hindered H. armigera growth and development. FNP could enhance RNAi efficiency to achieve pest control by SCP-2 -targeted FNP-RNAi.
Keyphrases
- cancer therapy
- induced apoptosis
- gene expression
- cell cycle arrest
- aedes aegypti
- drug delivery
- hyaluronic acid
- dna methylation
- signaling pathway
- high resolution
- high throughput
- endoplasmic reticulum stress
- quantum dots
- binding protein
- zika virus
- risk assessment
- small molecule
- drosophila melanogaster
- cell proliferation
- single cell