Insect resistance to Bacillus thuringiensis (Bt) insecticidal proteins has rapidly evolved with the expansion of the planting area of transgenic Bt crops. Pyramiding RNA interference (RNAi) and Bt in crops is urgently needed to counter the rapid increase in pest resistance. The ideal “pyramid” strategy simultaneously targets different action pathways that exert synergetic effects on each other. Here, we identified a dephosphatase, namely, Helicoverpa armigera calcineurin (HaCAN), which might enhance the insecticidal activity of Cry1Ac against Helicoverpa armigera by regulating immune gene expression via dephosphatase activity, but not by acting as a receptor. Notably, blocking enzyme activity or knocking down endogenous HaCAN significantly promoted the enhancement in Cry1Ac toxicity to insect larvae and cells. Correspondingly, the increase in HaCAN activity reduced the cytotoxicity of Cry1Ac as shown by the heterologous expression of HaCAN. Our results provide a probable that HaCAN is an important candidate gene for pyramiding RNAi and Cry1Ac crops to control cotton bollworm.
Bacillus thuringiensis (Bt) is the safest, economically successful entomopathogen to date. It is extensively produced in transgenic crops or used in spray formulations to control Lepidopteran pests. The most serious threat to the sustainable usage of Bt is insect resistance. The resistance mechanisms to Bt toxins depend not only on alterations in insect receptors, but also on the enhancement of insect immune responses. In this work, we review the current knowledge of the immune response and resistance of insects to Bt formulations and Bt proteins, mainly in Lepidopteran pests. We discuss the pattern recognition proteins for recognizing Bt, antimicrobial peptides (AMPs) and their synthetic signaling pathways, the prophenoloxidase system, reactive oxygen species (ROS) generation, nodulation, encapsulation, phagocytosis, and cell-free aggregates, which are involved in immune response reactions or resistance to Bt. This review also analyzes immune priming, which contributes to the evolution of insect resistance to Bt, and puts forward strategies to improve the insecticidal activity of Bt formulations and manage insect resistance, targeting the insect immune responses and resistance.
Insect resistance to Bacillus thuringiensis (Bt) toxins has led to an urgent need to explore the insecticidal
mechanisms of Bt. Previous studies indicated that Helicoverpa
armigera ATP synthase subunit α (HaATPs-α)
is involved in Cry1Ac resistance. In this study, a real-time quantitative
polymerase chain reaction (RT-PCR) confirmed that HaATPs-α expression was significantly reduced in the Cry1Ac-resistant
strain (BtR). Cry1Ac feeding induced the downregulated expression
of HaATPs-α in the susceptible strain, but
not in the BtR strain. Furthermore, the interaction between HaATPs-α
and Cry1Ac was verified by ligand blotting and homologous competition
experiments. The in vitro gain and loss of function
analyses showed HaATPs-α involved in Cry1Ac toxicity by expressing
endogenous HaATPs-α and HaATPs-α double-stranded RNAs
in Sf9 and midgut cells, respectively. Importantly, purified HaATPs-α
synergized Cry1Ac toxicity to H. armigera larvae. These findings provide the first evidence that HaATPs-α
is a potential receptor of Cry1Ac, it shows downregulated participation
in Cry1Ac resistance, and it exhibits higher enhancement of Cry1Ac
toxicity to H. armigera larvae.
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