Chickpea
pod borer, Helicoverpa armigera, 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 Helicoverpa faces problems of degradation
by nucleases and insect gut pH. We demonstrate that chitosan nanoparticles
(CNPs) effectively mediate specific dsRNA delivery against Helicoverpa armigera juvenile hormone methyltransferase (JHAMT) and acetylcholine esterase (ACHE) 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 H. armigera JHAMT and ACHE 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 Spodoptera litura and Drosophila melanogaster 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.