Azadirachtin has been used to control agricultural pests
for a
long time; however, the molecular mechanism of azadirachtin on lepidopterans
is still not clear. In this study, the fourth instar larvae of fall
armyworm were fed with azadirachtin, and then the ecdysis was blocked
in the fourth instar larval stage (L4). The prothoracic glands (PGs)
of the treated larvae were dissected for RNA sequencing to determine
the effect of azadirachtin on ecdysis inhibition. Interestingly, one
of the PG-enriched genes, the nuclear hormone receptor 3 (HR3), was decreased after azadirachtin treatment, which
plays a critical role in the 20-hydroxyecdysone action during ecdysis.
To deepen the understanding of azadirachtin on ecdysis, the HR3 was knocked out by using the CRISPR/Cas9 system, while
the HR3 mutants displayed embryonic lethal phenotype;
thus, the stage-specific function of HR3 during larval
molting was not enabled to unfold. Hence, the siRNA was injected into
the 24 h L4 larvae to knock down HR3. After 96 h,
the injected larvae were blocked in the old cuticle during ecdysis
which is consistent with the azadirachtin-treated larvae. Taken together,
we envisioned that the inhibition of ecdysis in the fall armyworm
after the azadirachtin treatment is due to an interference with the
expression of HR3 in PG, resulting in larval mortality.
The results in this study specified the understanding of azadirachtin
on insect ecdysis and the function of HR3 in lepidopteran in vivo.