Nanobioscience Group, Agharkar Research Institute, Pune 411004, India.
Savitribai Phule Pune University, Pune 411007, India.
ACS Appl Bio Mater. 2021 Jun 21;4(6):5145-5157. doi: 10.1021/acsabm.1c00349. Epub 2021 Jun 4.
Chickpea pod borer, , displays resistance to chemical insecticides and transgenics. The potential nontransformative RNAi approach of specific gene silencing by mRNA breakdown through exogenous double-stranded (dsRNA) delivery to faces problems of degradation by nucleases and insect gut pH. We demonstrate that chitosan nanoparticles (CNPs) effectively mediate specific dsRNA delivery against () and ( target genes. Ionotropically synthesized cationic CNPs (100 nm size, +32 mV charge) loaded dsRNA efficiently and protected it effectively from degradation by nucleases and insect gut pH. Tagging CNPs with Calcofluor fluorescence illustrated its efficient uptake in columnar insect gut cells. The potential of CNPs-mediated dsRNA delivery was elucidated with effective silencing of green fluorescent protein transformed Sf9 cells. Furthermore, CNPs-dsRNA complexes were stable for 5 d on leaf surfaces, and their ingestion with leaf effectively silenced and genes to suppress related enzyme activities and caused 100% insect mortality. Further, in planta bioassay with CNPs-dsRNA spray confirmed the RNAi induced insect mortality. Moreover, CNPs-dsRNA fed nontarget insects and were unaffected, and no toxicity was observed for CNPs in cell line studies. Remarkably, only two low dose (0.028 g/ha) topical CNPs-ache-dsRNA sprays on chickpea displayed reduced pod damage with high yields on par with chemical control in the field, which was followed by CNPs-jhamt-dsRNA nanoformulation. These studies can pave the way for the development of topical application of CNPs-dsRNA spray as a safe, specific, innovative insecticide for sustainable crop protection.
斑衣蜡蝉,表现出对化学杀虫剂和转基因的抗性。通过外源性双链 RNA(dsRNA)递送到 进行特定基因沉默的潜在非转化 RNAi 方法面临核酸酶降解和昆虫肠道 pH 值的问题。我们证明壳聚糖纳米粒子(CNPs)有效地介导针对 ()和 (靶基因的特异性 dsRNA 传递。离子合成的阳离子 CNPs(100nm 大小,+32mV 电荷)有效地负载 dsRNA,并有效地保护其免受核酸酶和昆虫肠道 pH 值的降解。用 Calcofluor 荧光标记 CNPs 说明了其在柱状昆虫肠道细胞中的有效摄取。通过对转绿色荧光蛋白的 Sf9 细胞进行有效沉默,阐明了 CNPs 介导的 dsRNA 传递的潜力。此外,CNPs-dsRNA 复合物在叶片表面稳定 5 天,其与叶片的摄入有效地沉默了 和 基因,抑制了相关酶活性,并导致 100%的昆虫死亡。此外,在植物体内用 CNPs-dsRNA 喷雾进行的生物测定证实了 RNAi 诱导的昆虫死亡率。此外,CNPs-dsRNA 喂养的非靶标昆虫 和 不受影响,并且在细胞系研究中未观察到 CNPs 的毒性。值得注意的是,仅两次低剂量(0.028g/ha)对斑衣蜡蝉的局部 CNPs-ache-dsRNA 喷雾处理就降低了豆荚损伤,田间产量与化学对照相当,随后是 CNPs-jhamt-dsRNA 纳米制剂。这些研究可以为开发局部应用 CNPs-dsRNA 喷雾作为一种安全、特异、创新的杀虫剂用于可持续作物保护铺平道路。