Jul 2026· Journal of the Entomological Research Society· 0 citations· 39 references
TL;DR
Qualitative molecular insights into the midgut-level responses of H. armigera to EMB exposure are provided and further quantitative estimation of the altered levels of proteins can help formulation of an effective management strategy.
Abstract
Helicoverpa armigera is a major polyphagous pest with an immense potential to develop resistance to conventional insecticides. Emamectin benzoate (EMB), a compound derived from abamectin, is widely used for its efficacy against lepidopteran larvae. Despite several studies revealing its toxic and growth regulatory effects, information regarding its effects on midgut protein composition remains limited. In this study, we examined the midgut protein profile of H. armigera larvae following exposure to dietary EMB. Midgut proteins were separated by SDS-PAGE and differentially obtained bands were identified using liquid chromatography-mass spectrometry (LC-MS). The EMB-treated larvae showed a total of 39 differential proteins, among which 35 proteins were differentially deleted while just 4 proteins were differentially detected. The chief differentially absent proteins were found to be associated with metabolism, protein processing, signal transduction and stress response, while the differentially detected proteins were related to glycolysis and signal transduction. The differential absence/presence of these proteins indicated their plausible role in causing the disrupted metabolic and physiological processes in EMB-treated H. armigera larvae. This study provides qualitative molecular insights into the midgut-level responses of H. armigera to EMB exposure. However, further quantitative estimation of the altered levels of proteins can help formulation of an effective management strategy.
Background: Imidacloprid, a widely used neonicotinoid insecticide, is routinely applied to control pests in Astragalus membranaceus var. mongholicus, a crucial medicinal herb producing Astragali Radix. However, the early short-term transcriptional and metabolic responses of its seedlings under imidacloprid gradient stress remain poorly characterized. Methods: In this study, 80-day seedlings were subjected to three foliar spray treatments: blank control (CK), the recommended imidacloprid concentration (2000-fold dilution, 475 mg·L−1), and an excessively high concentration (500-fold dilution, 1900 mg·L−1). Leaf samples were harvested 24 h post-treatment for untargeted ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC–MS/MS) metabolomics (6 biological replicates) and RNA-seq transcriptome sequencing (3 biological replicates). Results: The low- and high-dose treatments induced 1076 and 860 differential metabolites and 6818 and 7283 differentially expressed genes, respectively. Flavonoids, saponins, terpenoids, amino acid metabolites, and energy-related pathways were prominently affected. KEGG enrichment indicated activation of flavone/flavonol biosynthesis, phenylpropanoid metabolism, amino acid metabolism, MAPK signaling, cutin/suberin/wax biosynthesis, and ABC transporter pathways, whereas high-dose exposure was associated with stronger changes in genes related to DNA replication and cell wall remodeling. Integrated network analysis highlighted CHS, PAL, MYC2, KCS, and ABCG40 as candidate regulators linking stress signaling, secondary metabolism, and metabolite transport. Conclusions: Seedlings of A. membranaceus var. mongholicus exhibit dose-dependent acute responses to imidacloprid. Moderate pesticide exposure primarily activates defensive secondary metabolism, whereas excessive dosage triggers genome-wide transcriptional reprogramming. This work identifies key metabolic pathways and hub genes, offering candidate molecular markers for investigating pesticide stress adaptation in medicinal Astragalus and guiding standardized pesticide application in cultivation.
Dabao Yin, Xue Li, Li Zhou et al.· Genes· 0 citations
Findings provide insights into the potential multifaceted insecticidal action of benzothiazole in T. castaneum at the transcriptomic level and support its further development as a target-specific grain fumigant.
Kaidi Cui, Xueran Hu, Weifeng Cheng et al.· Pest Management Science· 0 citations
The antennal gland (AnG) of decapod crustaceans has been proposed as a potential source of bioactive molecules involved in chemical communication; however, its protein composition remains largely unexplored. Here, we present the first reference proteomic map of the aqueous extract from the antennal gland of the Pacific white shrimp Litopenaeus vannamei. Protein extracts from immature and mature females were analyzed using an integrated workflow combining one-dimensional SDS-PAGE, reverse-phase high-performance liquid chromatography (RP-HPLC), and nanoLC-tandem mass spectrometry. Electrophoretic and chromatographic analyses revealed a high degree of qualitative similarity between reproductive stages. SDS-PAGE resolved six major protein bands (~227, 166, 77, 42, 35, and 17 kDa), most comprising multiple co-migrating proteins as revealed by LC-MS/MS. Hemocyanin was identified as the predominant protein and was detected across several electrophoretic bands. Additional proteins were associated with innate immunity, including β-1,3-glucan-binding protein and coagulable hemolymph protein; reproductive processes, including vitellogenin, spermatogonial stem-cell renewal factor, farnesoic acid O-methyltransferase, estrogen sulfotransferase, and prostaglandin reductase 1; as well as energy metabolism, protein homeostasis, cytoskeletal organization, and intracellular trafficking. Because several identified proteins are widely distributed or known hemolymph components, their detection cannot be assumed to reflect AnG-specific expression or function. Collectively, these findings establish a molecular reference for the L. vannamei AnG and reveal protein components associated with multiple physiological processes. This dataset provides a proteomic framework for future comparative and functional studies aimed at elucidating antennal gland physiology and experimentally evaluating the potential involvement of proteinaceous or peptide-based molecules in chemical communication in decapod crustaceans.
J. Alvarado-Mesén, Rodolfo Umaña-Castro, Julián Fernández et al.· General and Comparative Endo...· 0 citations
The fall armyworm (S. frugiperda) has developed resistance to numerous insecticides and is currently considered one of the most destructive pests threatening global crop production. Consequently, the development of environmentally sustainable pest management strategies has become increasingly important. Insect-associated pathogenic bacteria represent a promising source of bioactive metabolites with potential insecticidal properties. In the present study, pathogenic bacteria associated with S. frugiperda were isolated and molecularly identified as Serratia marcescens strain INS420 based on 16 S rRNA gene sequencing. The secondary metabolites produced by this bacterium demonstrated significant insecticidal activity under both laboratory and field conditions. Metabolic profiling of the extracted compounds was performed using liquid chromatography–mass spectrometry (LC–MS) and gas chromatography–mass spectrometry (GC–MS), revealing the presence of several bioactive compounds, including diketopiperazines, fatty acids and their esters, squalene, phthalate derivatives, and a cardenolide. To gain insights into the potential mechanism of action, molecular docking simulations were conducted to evaluate the binding affinity of the identified metabolites with S. frugiperda acetylcholinesterase (AChE). Among the detected compounds, squalene and several fatty acid derivatives exhibited stable interactions within the active site of the enzyme, suggesting a possible inhibitory effect on AChE activity. Collectively, these findings demonstrate that S. marcescens associated with S. frugiperda produces metabolites with notable insecticidal potential and highlight insect-associated pathogenic bacteria as a valuable source of bioactive compounds for the sustainable management of fall armyworm.
Kreema A. El-Lebody, Ramy E. El-Ansary, Shaimaa A. Nour et al.· Scientific Reports· 0 citations
Corynespora leaf spot, caused by Corynespora cassiicola, is an emerging disease in crops that significantly impacts both yield and quality. Currently, the use of fungicides to control Corynespora leaf spot has led to the development of varying degrees of resistance in the pathogen. Therefore, it is crucial to screen for highly effective fungicides with novel modes of action. This study evaluated the antifungal activity of 1-hydroxyphenazine (1OH-PHZ) against multiple phytopathogenic fungi, with a half-maximal effective concentration (EC50) of 19.23 μg/ml against C. cassiicola hyphae. In vivo assay demonstrated antifungal activity of 67.22 and 45.03% on detached tomato leaves and fruits, respectively, at a dose of 500.0 μg/ml. Microscopic and ultrastructural observations revealed hyphal collapse, surface wrinkling, and indistinct organelle boundaries following treatment. Integrated transcriptomic and metabolomic analyses showed differentially expressed genes and differentially abundant metabolites, primarily affecting amino acid metabolism and biosynthesis pathways. Molecular docking, dynamic simulations, and microscale thermophoresis assays demonstrated that 1OH-PHZ binds to PLP-dependent transferase (PLPDT), exhibiting a binding free energy of -7.2 kcal/mol and a dissociation constant (Kd) value of 1.16 μM. Collectively, these findings suggest that 1OH-PHZ potentially binds to PLPDT, thereby disrupting amino acid metabolism and biosynthesis, which subsequently affects the synthesis and morphological development of the fungal cell wall and cell membrane. Through the combination and screening of highly active fungicidal substances, this study offers mechanistic insights that support the potential development of 1OH-PHZ as a novel agricultural fungicide for managing C. cassiicola infections.
Dongxue Li, Haowen Ni, Yuqi Bin et al.· Phytopathology· 0 citations
Coptotermes formosanus, a worldwide pest, inflicts large losses on agriculture, forestry, construction, and other industries. As efficient, environmentally friendly pest control methods, microbial biopesticides are widely used to manage major pests. We previously isolated an Akanthomyces lecanii strain with strong insecticidal activity against termites. However, the interaction between the biocontrol agent and termites is still unknown. In this study, PacBio single-molecule real-time (SMRT) sequencing technology and Illumina RNA-seq sequencing technology were used to explore the transcriptomic differences in C. formosanus before and after A. lecanii infection. A total of 7,882,407 full-length transcripts were obtained. Single genes were further annotated using the NR, GO, KEGG, COG/KOG, Swiss-Prot, and KEGG homology public databases. A total of 2,782 differentially expressed genes were identified, including 1,440 upregulated genes and 1,342 downregulated genes. The expression of the Toll signaling pathway, mitogen-activated protein kinase (MAPK) pathway, detoxification metabolism, and immune-related genes, including scavenger receptor, apolipophorin, Cdc42, Integrin, Toll, serine protease, and transferrin genes, may be related to A. lecanii infection. This work not only greatly enriches the gene annotation resources of C. formosanus but also provides a new perspective for understanding the fungal immune defense mechanisms of social insects at the molecular level. These findings provide a theoretical basis for the development of new immunosuppressive agents.
K. Feng, Qi Ye, Yi-Yang Zhao et al.· Sociobiology· 0 citations
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