Pyriproxyfen (PPF) has been shown to affect the pupal stage and ecdysone levels in holometabolous insects, such as silkworms and mealworms. It remains unknown whether it affects hemimetabolous insects with their hormone levels in insects lacking a pupal stage. In this laboratory study, bioassays were conducted to investigate the effects of varying doses of PPF on Aphis craccivora Koch (Hemiptera: Aphididae). Ultraperformance liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) was used to determine the types and titers of juvenile hormone (JH) and 20-hydroxyecdysone (20E). Additionally, the effects of PPF on A. craccivora reproduction and molting, as well as its influence on relevant gene expression, were examined. The results revealed LC₅₀ and LC₉₀ values of 3.84 and 7.49 mg/l for PPF, respectively, after 48 h of exposure. The results demonstrated a significant reduction in the titer of JH III and a significant increase in the titer of 20E following treatment with PPF. However, there was no significant decrease observed in the titer of JH III skipped bisepoxide (JH SB3). A sublethal concentration of PPF was found to inhibit Krüppel homolog 1 (kr-h1) gene expression and reduce aphid reproduction, but it did not significantly impact ecdysone receptor expression and aphid molting. The results of this study demonstrate that PPF exhibits a lethal effect on aphids, thereby providing an effective means of control. Additionally, sublethal concentrations of PPF have been found to inhibit the JH in aphids, resulting in a decline in their reproductive ability and achieving the desired control objectives.

Juvenile hormones (JHs) play a crucial role in the development of the fall armyworm, Spodoptera frugiperda, with varying types and concentrations observed at different stages. However, the interplay between JHs and 20-hydroxyecdysone (20E) in co-ordinating the life cycle of S. frugiperda remains unknown. In this study, by using high-precision UPLC-MS/MS and qRT-PCR, we detected changes in JH and 20E levels and identified important 20E receptor and response genes. Our findings revealed that JH I antagonises JH II, whereas JH II promotes JH III synthesis. High JH I and JH II concentrations in the larval stage strongly affected moulting to the next instar. Furthermore, these hormones inhibit 20E synthesis and reduce its receptor expression, thereby affecting 20E signalling. During pupation, JH II plays a crucial role in stimulating 20E synthesis for larval–pupal transformation. JH I and JH II are essential for eclosion, precisely controlling emergence timing and subsequent reproductive organ maturation. These hormones likely regulate larval development, pupation, and adult reproduction in S. frugiperda. Further studies are warranted to explore the regulatory advantages of JH I and JH II over JH III.

Spodoptera frugiperda (J.E. Smith) is a crucial agricultural pest owing to its global impact on >300 crops. Among these, the corn strain of S. frugiperda causes significant damage to maize (Zea mays L.). However, limited research exists on the influence of maize nutrients on the metamorphosis of S. frugiperda and the underlying mechanisms. In this study, the effects of different growth stages of maize leaves, namely, tender leaves (tender) and mature leaves (mature), on various aspects of larval development, including body weight, body length, developmental age, pupation rate, and eclosion rate, were investigated. Additionally, we measured the levels of 20-hydroxyecdysone (20E) and three types of juvenile hormone (JH; i.e., JH I–III) in S. frugiperda larvae fed on tender or mature. The results revealed that larvae fed on Tender exhibited significantly prolonged instar duration, reduced body weight and length, and decreased pupation and eclosion rates, with the emergence of abnormal adults. Analysis of nutritional components in maize leaves revealed significantly higher levels of amino acids, soluble sugars, and sterols in mature than in tender. Hormone analysis in S. frugiperda larvae revealed higher 20E titers in individuals feeding on mature during prepupal and pupal stages. We demonstrated the crucial role of sterols in regulating the level of 20E and pupation rate of S. frugiperda. Based on these findings, we propose that isoleucine, arginine, glutamic acid, sucrose, campesterol, and β-sitosterol serve as key nutrients influencing the development of S. frugiperda. Moreover, β-sitosterol is a significant factor influencing the interaction between maize leaves and S. frugiperda. Our research results provide a reference for the control strategy of S. frugiperda based on breeding insect-resistant varieties by altering host nutrition.

Cereal cyst nematode (Heterodera avenae), an important plant-parasitic nematode causing yield losses of wheat, has been found in many provinces in China. It is urgent to develop an effective method of protecting wheat from H. avenae damage. Because of its novel mode of action, fluopyram has been registered for controlling root-knot nematodes on cucumber and tomato in China. However, the bioactivity of fluopyram against H. avenae and whether this seed treatment can effectively control H. avenae on wheat remains unknown. In this study, a bioactivity assay revealed that fluopyram increased the mortality of H. avenae second-stage juveniles (J2), with lethal concentrations (LC) required to kill 50% (LC50) and 90% (LC90) of 0.92 mg⋅liter⁻¹ and 2.92 mg⋅liter⁻¹_, respectively. Hatching tests showed that the H. avenae egg hatching percent was reduced by 35.2 to 69.2% with fluopyram at rates of 1.6 to 6.4 mg⋅liter⁻¹, and that the egg hatching period was delayed by 3 to 9 days compared with the control. During pot and field trials, fluopyram seed treatment significantly reduced the H. avenae population density and increased wheat yield by 3.0 to 13.7%. Therefore, fluopyram seed treatment is an effective approach for the management of H. avenae on wheat in China.