Engineered nanomaterials interfaced with plant seeds can improve stress tolerance during the vulnerable seedling stage. Herein, we investigated how priming seeds with antioxidant poly(acrylic acid)-coated cerium oxide nanoparticles (PNC) impacts cotton (Gossypium hirsutum L.) seedling morphological, physiological, biochemical, and transcriptomic traits under salinity stress. Seeds primed with 500 mg L⁻¹ PNC in water (24 h) and germinated under salinity stress (200 mM NaCl) retained nanoparticles in the seed coat inner tegmen, cotyledon, and root apical meristem. Seed priming with PNC significantly (P < 0.05) increased seedling root length (56%), fresh weight (41%), and dry weight (38%), modified root anatomical structure, and increased root vitality (114%) under salt stress compared with controls (water). PNC seed priming led to a decrease in reactive oxygen species (ROS) accumulation in seedling roots (46%) and alleviated root morphological and physiological changes induced by salinity stress. Roots from exposed seeds exhibited similar Na content, significantly decreased K (6%), greater Ca (22%) and Mg content (60%) compared to controls. A total of 4779 root transcripts were differentially expressed by PNC seed priming alone relative to controls with no nanoparticles under non-saline conditions. Under salinity stress, differentially expressed genes (DEGs) in PNC seed priming treatments relative to non-nanoparticle controls were associated with ROS pathways (13) and ion homeostasis (10), indicating that ROS and conserved Ca²⁺ plant signaling pathways likely play pivotal roles in PNC-induced improvement of salinity tolerance. These results provide potential unifying molecular mechanisms of nanoparticle-seed priming enhancement of plant salinity tolerance.

Goosegrass (Eleusine indica L.), a serious annual weed in the world, has evolved resistance to several herbicides including paraquat, a non-selective herbicide. The mechanism of paraquat resistance in weeds is only partially understood. To further study the molecular mechanism underlying paraquat resistance in goosegrass, we performed transcriptome analysis of susceptible and resistant biotypes of goosegrass with or without paraquat treatment. The RNA-seq libraries generated 194,716,560 valid reads with an average length of 91.29 bp. De novo assembly analysis produced 158,461 transcripts with an average length of 1153.74 bp and 100,742 unigenes with an average length of 712.79 bp. Among these, 25,926 unigenes were assigned to 65 GO terms that contained three main categories. A total of 13,809 unigenes with 1,208 enzyme commission numbers were assigned to 314 predicted KEGG metabolic pathways, and 12,719 unigenes were categorized into 25 KOG classifications. Furthermore, our results revealed that 53 genes related to reactive oxygen species scavenging, 10 genes related to polyamines and 18 genes related to transport were differentially expressed in paraquat treatment experiments. The genes related to polyamines and transport are likely potential candidate genes that could be further investigated to confirm their roles in paraquat resistance of goosegrass. This is the first large-scale transcriptome sequencing of E. indica using the Illumina platform. Potential genes involved in paraquat resistance were identified from the assembled sequences. The transcriptome data may serve as a reference for further analysis of gene expression and functional genomics studies, and will facilitate the study of paraquat resistance at the molecular level in goosegrass.

The widespread use of lead (Pb) has led to serious environmental and human health problems worldwide. The application of oxide nanoparticles (CeO₂ NPs) in alleviating abiotic stress in plants has received extensive attention. In this study, 50 mg·L⁻¹ CeO₂ NPs can improve Pb resistance and promote rice growth. Specifically, this study observed that CeO₂ NPs increased the activity of antioxidant enzymes peroxidase (POD), catalase (CAT), and ascorbate peroxidase (APX), but the difference did not reach a significant level. At the same time, CeO₂ NPs upregulated antioxidant metabolites alpha-linolenic acid, linoleic acid, ferulic acid, and kaempferol under Pb stress. In addition, CeO₂ NPs upregulated multiple defense response-related genes, such as OsOPR1 and OsPR10a; RPR10a, and improved rice carbon flow and energy supply by upregulating sucrose and D-glucose. The results of this study provided technical support for alleviating Pb stress in rice.

The interdisciplinary progress in nanotechnology has yielded environmentally friendly and cost-effective strategies to enhance bioherbicidal efficacy. This study presents the biosynthesis of silver nanoparticles (M-AgNPs) using the fungus Exserohilum rostratum, specifically targeting the Leptochloa chinensis weed in paddy fields. The M-AgNPs were characterized with an aqueous solution size of 107.9 nm and a zeta potential of −24.0 ± 0.20 mV, and their properties were analyzed by UV-Vis spectrophotometry, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR). The application of M-AgNP suspension at different concentrations of 70 µg∙mL⁻¹, 80 µg∙mL⁻¹, and 100 µg∙mL⁻¹ to L. chinensis at the 3–4 leaf stage resulted in significant herbicidal effects. These nanoparticles induced oxidative stress and significantly reduced the activities of peroxidase, catalase, and superoxide dismutase in the weed seedlings. Meanwhile, M-AgNP treatments significantly increased the activity of cell wall-degrading enzymes, including polygalacturonase and cellulase, in L. chinensis leaves and caused organelle damage in plant leaf cells. Safety assessments showed no significant impact on rice growth after treatment with M-AgNP₃ (100 µg∙mL⁻¹) suspension. Our results suggest that M-AgNPs represent a sustainable and eco-friendly approach to weed control that is compatible with rice cultivation, thus supporting the adoption of green agricultural practices.

Background: Manual topping is a routine agronomic practice for balancing the vegetative and reproductive growth of cotton (Gossypium hirsutum) in China, but its cost-effectiveness has decreased over time. Therefore, there is an urgent need to replace manual topping with new approaches, such as biological topping. In this study, we examined the function of GhREV transcription factors (a class III homeodomain-leucine zipper family, HD-ZIP III) in regulating the development of shoot apical meristem (SAM) in cotton with the purpose of providing candidate genes for biological topping of cotton in the future.Results: We cloned four orthologous genes ofAtREVin cotton, namelyGhREV1,GhREV2,GhREV3, andGhREV4. All theGhREVsexpressed in roots, stem, leaves, and SAM. Compared withGhREV1andGhREV3, the expression level ofGhREV2andGhREV4was higher in the SAM. However, only GhREV2 had transcriptional activity. GhREV2 is localized in the nucleus; and silencing it via virus-induced gene silencing (VIGS) produced an abnormal SAM. Two key genes, GhWUSA10 and GhSTM, which involved in regulating the development of plant SAM, showed about 50% reduction in their transcripts in VIGS-GhREV2plants.Conclusion: GhREV2 positively regulates the development of cotton SAM by regulatingGhWUSA10andGhSTM potentially.