Xingtao Qie

BACKGROUND: Phyma leptostachya is a traditional insecticidal plant that has been employed as a natural insecticide for the control of various pests. Nanotechnology possesses transformative potential in the field of crop protection and contributes to the optimal utilization and outstanding performance of plant extracts. Hence, the preparation process of P. leptostachya extract‐loaded nanoemulsions was investigated in this study, as well as the aphicidal activity and safety to non‐target organisms. RESULTS: Nanoemulsion formulated with the emulsifier EL‐60 demonstrated superior stability. Furthermore, the stability of these nanoemulsions was found to enhance with increasing emulsifier concentrations, ranging from 1% to 5%. The optimized formulation of nanoemulsion was formed as follows: 0.2% P. leptostachya extract, 2% S‐200, 3% EL‐60, and 94.8% deionized water. Finally, P. leptostachya extract‐loaded nanoemulsion showed excellent insecticidal activity against Acyrthosiphon pisum with LC ₅₀ 0.2267 mg/mL at 24 h. The LC ₅₀ of nanoemulsion to earthworm was much higher than 10 mg/kg dried soil, indicating nanoemulsion has good safety. In addition, nanoemulsion had no effect on the plant height of Vicia faba and bolster its antioxidant systems. CONCLUSION: This research has enabled the design and fabrication of nanoemulsions loaded with P. leptostachya extract, which serve as a novel insecticide aimed at enhancing insecticidal efficacy with low toxicity that is beneficial to the sustainable control of pests. © 2025 Society of Chemical Industry.

Monolepta signata is a polyphagous and highly destructive agricultural pest, currently only distributed in Asia. In its place of origin, it poses a serious threat to important economic crops, for instance, maize (Zea mays L.) and cotton (Gossypium hirsutum L.). Based on morphological and molecular data research, it has been found that M. quadriguttata (Motschulsky), M. hieroglyphica (Motschulsky), and M. signata are actually the same species. This discovery means that the range of this pest will expand, and it also increases the risk of it spreading to non-native areas worldwide. It is crucial for global agricultural production to understand which countries and regions are susceptible to invasion by M. signata and to formulate corresponding prevention, control, and monitoring strategies. This study uses the maximum entropy model, combined with bioclimatic variables and elevation, to predict the potentially suitable areas and diffusion patterns of M. signata worldwide. The results indicate that in its suitable area, M. signata is mainly affected by three key climatic factors: Precipitation of Wettest Month (bio13), Mean Temperature of Warmest Quarter (bio10), and Temperature Seasonality (bio4). Under the current status, the total suitable region of M. signata is 252,276.71 × 10⁴ km². In addition to its native Asia, this pest has potentially suitable areas in Oceania, South America, North America, and Africa. In the future, with climate change, the suitable area of M. signata will expand to high-latitude areas and inland areas. This study found that by the 2070s, under the SSP5-8.5 climate scenario, the change in the potentially suitable area of this insect is the largest. By identifying the potentially suitable areas and key climatic factors of M. signata, we can provide theoretical and technical support to the government, enabling them to more effectively formulate strategies to deal with the spread, outbreak, and invasion of M. signata.

Sex pheromones, which consist of multiple components in specific ratios promote intraspecific sexual communications of insects. Plutella xylostella (L.) is a worldwide pest of cruciferous vegetables, the mating behavior of which is highly dependent on its olfactory system. Long trichoid sensilla on male antennae are the main olfactory sensilla that can sense sex pheromones. However, the underlying mechanisms remain unclear. In this study, 3 sex pheromone components from sex pheromone gland secretions of P. xylostella female adults were identified as Z11‐16:Ald, Z11‐16:Ac, and Z11‐16:OH in a ratio of 9.4 : 100 : 17 using gas chromatography – mass spectrometry and gas chromatography with electroantennographic detection. Electrophysiological responses of 581 and 385 long trichoid sensilla of male adults and female adults, respectively, to the 3 components were measured by single sensillum recording. Hierarchical clustering analysis showed that the long trichoid sensilla were of 6 different types. In the male antennae, 52.32%, 5.51%, and 1.89% of the sensilla responded to Z11‐16:Ald, Z11‐16:Ac, and Z11‐16:OH, which are named as A type, B type, and C type sensilla, respectively; 2.93% named as D type sensilla responded to both Z11‐16:Ald and Z11‐16:Ac, and 0.34% named as E type sensilla were sensitive to both Z11‐16:Ald and Z11‐16:OH. In the female antennae, only 7.53% of long trichoid sensilla responded to the sex pheromone components, A type sensilla were 3.64%, B type and C type sensilla were both 0.52%, D type sensilla were 1.30%, and 1.56% of the sensilla responded to all 3 components, which were named as F type sensilla. The responding long trichoid sensilla were located from the base to the terminal of the male antennae and from the base to the middle of the female antennae. The pheromone mixture (Z11‐16:Ald : Z11‐16:Ac : Z11‐16:OH = 9.4 : 100 : 17) had a weakly repellent effect on female adults of P. xylostella. Our results lay the foundation for further studies on sex pheromone communications in P. xylostella.

Chemosensory proteins (CSPs) are highly efficient carry tools to bind and deliver hydrophobic compounds, which play an important role in the chemosensory process in insects. The diamondback moth, Plutella xylostella L. (Lepidoptera: Plutellidae), is a cosmopolitan pest that attacks cruciferous crops. However, the detailed physiological functions of CSPs in P. xylostella remain limited to date. Here, we identified a typical CSP, named PxylCSP18, in P. xylostella and investigated its expression patterns and binding properties of volatiles. PxylCSP18 was highly expressed in antennae and head (without antennae), and the expression level in the male antennae of P. xylostella was obviously higher than that in the female antennae. Moreover, PxylCSP18 has a relatively broad binding spectrum. Fluorescence competitive binding assays showed that PxylCSP18 had strong binding abilities with 14 plant volatiles (Ki < 10 μM) that were repellent or attractive to P. xylostella. Notably, PxylCSP18 had no significant binding affinity to (Z)-11-hexadecenal, (Z)-11-hexadecenyl acetate, and (Z)-11-hexadecenyl alcolol, which are the pheromone components of P. xylostella. The attractive effects of trans-2-hexen-1-ol and isopropyl isothiocyanate to male adults and the attractive effects of isopropyl isothiocyanate and the repellent effects of linalool to female adults were significantly decreased after knocked down the expression of PxylCSP18. Our results revealed that PxylCSP18 might play an important role in host plant detection, avoidance of unsuitable hosts, and selection of oviposition sites; however, it does not participate in mating behavior. Overall, these results extended our knowledge on the CSP-related functions, which provided insightful information about CSP-targeted insecticides.

Plutella xylostella L. is a destructive pest affecting cruciferous vegetables, causing massive economic losses worldwide. Plant−based insecticides are considered promising insect control agents. The Angelica pubescens extract inhibited female oviposition, with an oviposition deterrence index (ODI) of 61.65% at 12.5 mg/mL. We aimed to identify the bioactive compounds in A. pubescens extract. The compounds from A. pubescens extract were analyzed using LC−MS techniques. The toxicity and behavioral responses of larvae and adults of P. xylostella to ten compounds were investigated. We found that the caryophyllene oxide and 3,4-dimethoxycinnamic acid inhibited female oviposition; the ODIs were 98.31% and 97.59% at 1.25 mg/mL, respectively. The A. pubescens extract, caryophyllene oxide, and 3,4-dimethoxycinnamic acid caused larval mortality, with LC₅₀ values of 21.31, 4.56, and 5.52 mg/mL, respectively. The EAG response of females was higher than that of males under A. pubescens extract conditions, while the EAG response of males was higher than that of females in caryophyllene oxide and 3,4-dimethoxycinnamic acid conditions. The A. pubescens extract and caryophyllene oxide showed repellent activity against both female and male adults, while the 3,4-dimethoxycinnamic acid did not elicit any notable behavioral responses from P. xylostella adults. A. pubescens extract and caryophyllene oxide are potential insecticides, oviposition deterrents, and behavioral regulators against P. xylostella, and they could be potential candidates for the development of biological insecticides to control P. xylostella.

Compared to other insects, the pea aphid Acyrthosiphon pisum has a reduced immune system with an absence of genes coding for a lot of immunity‐related molecules. Notably, nitric oxide synthase (NOS), which catalyses the synthesis of nitric oxide (NO), is present in the pea aphid. However, the role of NO in the immune system of pea aphid remains unclear. In this study, we explored the role of NO in the defence of the pea aphid against bacterial infections and found that the NOS gene of the pea aphid responded to an immune challenge, with the expression of ApNOS observably upregulated after bacterial infections. Knockdown of ApNOS using RNA interference or inhibition of NOS activity increased the number of live bacterial cells in aphids and the mortality of aphids after bacterial infection. Conversely, the increase in NO level in aphids using NO donor inhibited the bacterial growth, increased the survival of bacteria‐infected aphids, and upregulated immune genes, such as Toll pathway and phagocytosis related genes. Thus, NO promotes immune responses and plays an important role in the immune system of pea aphid.