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Cotton production is negatively impacted by many insect pests from multiple orders, resulting in significant agronomic and economic losses. This study utilized a comparative transcriptomic methodology to discover conserved gene targets with potential applications in pest management across four insect orders that infest cotton: Hemiptera, Lepidoptera, Orthoptera, and Thysanoptera. A total of 104 publicly available RNA-Seq datasets, representing 17 pest species were de novo assembled in two ways, first was classified by read length (PE100 and PE150) and secondly as species-specific transcriptomes, and their qualities were assessed (alignment ≥ 90%, BUSCO ≥ 80%). Functional annotation utilizing insect-specific databases and orthology-based filtering identified three highly conserved genes, namely Arginine kinase (ArgK), Ryanodine receptor (RyR), and Serine/Threonine Protein phosphatase (STPP). These genes are involved in critical physiological functions, including ATP regeneration, calcium ion homeostasis, and phosphorylation-dependent signaling, and were enriched in pathways associated with insect development and stress response, including as JAK/STAT signaling and chitin metabolism. The study aimed to find broad-spectrum targets across several taxa; however, Oxycarenus laetus, a prominent sap-sucking pest of cotton, was chosen for downstream validation because of its increasing importance and ease of access for experimental research. The expression of ArgK, RyR, and STPP in O. laetus was validated by qPCR, affirming the biological significance of these targets and their functional conservation. This integrated methodology, which includes cross-order comparative transcriptome analysis and species-specific validation, illustrates a scalable approach for discovering essential molecular targets with translational potential in pest control. The results establish a basis for the development of RNAi-based or chemical strategies designed for cotton pest control.
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http://dx.doi.org/10.1038/s41598-025-08880-9 | DOI Listing |
Exp Ther Med
October 2025
Section of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete, 71003 Heraklion, Greece.
Immune-related factors may serve an important role in the development of endometriosis, considering the occurrence of substantial abnormalities in the immune system of women with endometriosis, including reduced T-cell reactivity and natural killer cell cytotoxicity, as well as increased numbers and activation of peritoneal macrophages. Moreover, women suffering from endometriosis are at a higher risk for developing various autoimmune diseases as comorbidities of endometriosis. Recent epidemiological data demonstrate that patients with endometriosis have a significantly higher risk (2.
View Article and Find Full Text PDFHealth Sci Rep
September 2025
Department of Dermatology the Union Hospital, Fujian Medical University Fuzhou People's Republic of China.
Background And Aims: Several observational studies have reported inconsistent associations between dyslipidaemia, stains use and atopic dermatitis (AD). Nevertheless, the available data on the effects of -C-lowering as well as TG-lowering drugs remain inconclusive and limited. The aim of this study was to evaluate the causal association of lipid traits and long-term use of lipid-lowering drugs on AD risk.
View Article and Find Full Text PDFInt J Gen Med
September 2025
Department of Geriatrics, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, 610072, People's Republic of China.
Background: Sepsis is characterized by profound immune and metabolic perturbations, with glycolysis serving as a pivotal modulator of immune responses. However, the molecular mechanisms linking glycolytic reprogramming to immune dysfunction remain poorly defined.
Methods: Transcriptomic profiles of sepsis were obtained from the Gene Expression Omnibus.
Mol Ther Methods Clin Dev
June 2025
Precision Safety, Pharma Product Development, Roche Innovation Center Basel, CH-4070 Basel, Switzerland.
Adeno-associated virus (AAV) vectors are widely used in gene therapy, particularly for liver-targeted treatments. However, predicting human-specific outcomes, such as transduction efficiency and hepatotoxicity, remains challenging. Reliable models are urgently needed to bridge the gap between preclinical studies and clinical applications.
View Article and Find Full Text PDFMol Ther Methods Clin Dev
June 2025
Université Paris-Saclay, University Evry, Inserm, Genethon, Integrare Research Unit UMR_S951, 91000 Evry, France.
Pompe disease is a glycogen storage disorder caused by mutations in the acid α-glucosidase (GAA) gene, leading to reduced GAA activity and glycogen accumulation in heart and skeletal muscles. Enzyme replacement therapy with recombinant GAA, the standard of care for Pompe disease, is limited by poor skeletal muscle distribution and immune responses after repeated administrations. The expression of GAA in muscle with adeno-associated virus (AAV) vectors has shown limitations, mainly the low targeting efficiency and immune responses to the transgene.
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