Dinotefuran, a third-generation neonicotinoid insecticide, is widely used in agriculture production due to its excellent insecticidal efficacy. Considering its persistence and high toxicity in soil, it is essential to evaluate its low-dose toxic effects on non-target soil organisms such as the springtail (Folsomia candida). The results revealed that the 7-day half lethal concentration (7d-LC50) of dinotefuran contact toxicity to springtails was 0.029 mu g cm(-2). Its chronic toxicity in 4 soil types was ranked as: red soil (0.021 mg kg(-1)) > fluvo-aquic soil (0.040 mg kg(-1)) > artificial soil (0.049 mg kg(-1)) > black soil (0.085 mg kg(-1)). Soil organic matter (SOC), pH, and total nitrogen (TN) were identified as critical factors affecting dinotefuran toxicity. Biochemical assay results showed that environmental concentrations (0.2-1.6 mg kg(-1)) of dinotefuran induced oxidative stress and oxidative damage in springtails. Oxidative stress-related enzymes (including superoxide dismutase (SOD) and catalase (CAT)) and detoxification enzymes were subjected to initial activation at low dinotefuran concentrations, inhibition and re-activation at high concentration. Target enzyme acetylcholinesterase (AChE), malondialdehyde (MDA) content, and total protein content were inhibited with prolonged exposure time and increasing concentrations of dinotefuran. Molecular docking analysis showed that dinotefuran bound to the active sites of related enzymes, thus disrupting their structure and functions, eventually resulting in damages to physiological functions of springtails. In summary, this study deciphers the dinotefuran toxicological mechanism on soil springtails at environmental concentrations. Our findings lay theoretical basis for further assessing its pollution risk and managing its application.

Acanthamoeba castellanii is a widespread unicellular eukaryote found in diverse environments, including tap water, soil, and swimming pools. It is responsible for severe infections, such as Acanthamoeba keratitis and granulomatous amebic encephalitis, particularly in individuals with immunocompromisation. The ability of protozoans to form dormant and persistent cysts complicates treatment, as current therapies are ineffective against cyst stages and suffer from poor specificity and side effects. Nitroxoline, a quinoline derivative with well- established antibacterial, antifungal, and antiviral properties, is a promising therapeutic candidate. This study aimed to elucidate cellular signalling events that counteract the effects of nitroxoline. In this study, nitroxoline significantly reduced the viability of A . castellanii trophozoites in a dose- and time-dependent manner, inducing morphological changes and apoptosis. Transcriptomic analysis revealed substantial alterations in gene expression, including enrichment of metabolic pathways, DNA damage responses, and iron ion binding. Nitroxoline treatment upregulated genes involved in DNA repair and oxidative stress response while regulating genes in the methionine and cysteine cycles. It also decreased the mitochondrial membrane potential, HAS production, and total iron amount in A . castellanii. Bioinformatic analyses and molecular docking studies suggest direct interactions between nitroxoline and several A . castellanii proteins. Our research provides a comprehensive molecular map of the response of A . castellanii to nitroxoline, revealing significant changes in gene expression related to the stress response and metabolic pathways. These findings underscore the potential of nitroxoline as a potent anti- Acanthamoeba agent, offering new insights into its mechanism of action and paving the way for effective combinational therapeutic strategies.

Salinity stress is one of the main abiotic factors that negatively impact plant growth and productivity. Continuous exposure to NaCl leads to the accumulation of ions such as sodium (Na+), chloride (Cl-), and sulfate (SO(4)2(-)) in plant cells, impairing nutrient absorption and causing cellular and tissue damage. Therefore, it is necessary to find alternatives to mitigate the harmful effects of salinity stress in plants. This study aimed to evaluate the biochemical and morphological changes in Allium cepa exposed to different treatments of NaCl and lutein, both individually and in combination. Seeds (120) were germinated in Petri dishes containing NaCl (50 mM/mL) and lutein (256 mu g/mL and 512 mu g/mL) solutions, at pH 7.1. Then, the conductivity, the germination rate, and the biochemical and molecular analyses were performed. Combination of 256 mu g/mL lutein with 50 mM/mL NaCl demonstrated potential to reduce salinity-induced oxidative stress, suggesting the use of lutein as an effective mitigator against salt stress damage. Lutein showed a binding affinity of -7.19 kcal/mol with the onion target protein. These findings indicate that lutein may enhance plant resistance to adverse conditions, promoting greater survival and development. Further studies in other plant models are recommended to validate the use of lutein as a protective agent for agricultural management in saline soils.

Salinity stress is a major threat to agricultural productivity and sustainability, often causing irreversible damage to photosynthesis. Lavender, a valuable aromatic plant, experiences growth impacts under salt stress. However, the regulatory mechanisms of photosynthesis related to its adaptation to salt stress remain unclear. In this study, lavender was exposed to 0, 100, 200, and 300 mM NaCl for 28 days. It was observed that lavender effectively maintained chlorophyll stability when salt concentrations were below 200 mM and stress duration was under 21 days. The most effective model for lavender under salt stress was identified as a right-angled hyperbolic modified model. Under moderate salt stress (100 mM, 200 mM), genes such as LaPSB28, LaPSBS, and LaPSBR contributed to PSII core stability, enhanced photosynthetic pigment levels, and sustained high electron transfer rates to improve salt-tolerance. Additionally, LaLHCB4-1 and LaPSAK-1 regulated stomatal size, thereby facilitating gas exchange and supporting the photosynthetic process. Conversely, under high salt stress (300 mM), LaPSBW-1, -2, and LaPSAB were found to reduce photosynthetic pigment levels and inhibit photosynthetic activity. However, genes such as LaCHLG-2, LaGLG-3, LaBAM1-1 and -3, and LaCHLP-3 aided in starch synthesis by increasing pigment content, thus promoting energy balance and enhancing salt tolerance. This regulation involved photosynthesis-antenna proteins and pathways related to starch, sucrose, and chlorophyll metabolism. These findings may support the cultivation of salt-tolerant lavender varieties and maximize saline soil usage.

Root-knot nematode (RKN) (Meloidogyne incognita) is a major plant parasitic nematode that severely damages crops, leading to significant yield losses and substantial economic impact globally. This study aims to investigate an environmentally sustainable biological strategy for mitigating parasitic populations of the root-knot nematode, M. incognita. Specifically, the research focuses on assessing the nematicidal efficacy of Acalypha indica against M. incognita mortality and second-stage juveniles' (J2) hatching under controlled in vitro conditions. A. indica leaf aqueous extract was applied at varying concentrations (250, 500, 750, and 1000 ppm) to J2s and egg masses of M. incognita. Notably, at 1000 ppm, a significant increase in J2 mortality and hatching inhibition was observed, while 250 ppm concentration showed the least favorable outcome; with mortality rates ranging from 22-82%. Chemical analysis via gas chromatography-mass spectroscopy (GC-MS) identified Benzoic acid, Cyclooctasiloxane, and 3-Isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris (trimethylsiloxy) tetrasiloxane as predominant compounds. The nematicidal activity of A. indica leaf extract was further validated through in silico molecular docking, revealing that benzoic acid, Cyclooctasiloxane, and 3-Isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris (trimethylsiloxy) tetrasiloxane bind to the ODR 3 protein of M. incognita with binding energies of -15.72, -8.91, and -7.35 kJ/mol, respectively. These findings hold promise for environmentally benign root-knot nematode management, contributing to improved soil health.

Penthiopyrad, a chiral pesticide, has been widely used in agricultural production. However, systematic evaluation of stereoselective bioactivity and biotoxicity of penthiopyrad in soil environment is insufficient. In this study, the stereoselective bioactivity of penthiopyrad against three soil-borne disease pathogens and its stereoselective biotoxicity to soil non-target organisms were investigated. The present results showed that the bioactivities of S-penthiopyrad were 546, 76 and 1.1-fold higher than those of R-penthiopyrad due to their different interaction modes with SDH in different target pathogens. S-penthiopyrad was more persistent in the soil environment and had stronger bioaccumulation than R-penthiopyrad. The accumulation of penthiopyrad in earthworms induced the response of detoxification system, resulting in the significant increases in the activity of detoxifying enzymes, such as GST, CarE, and CYP450. Additionally, both S-penthiopyrad and R-penthiopyrad induced cell apoptosis, intestinal damage and differentially expressed genes in earthworms, especially S-penthiopyrad. Furthermore, S-penthiopyrad has stronger binding capacity with COL6A and ACE proteins, while Rpenthiopyrad has stronger binding capacity with CYP450 family proteins, which may be the main reason for the differences in biotoxicity between PEN enantiomers. Considering the differences in bioactivity and biotoxicity of penthiopyrad enantiomers, as well as the modes of action of pesticides on target and non-target organisms, Spenthiopyrad has greater potential for future development.

Fluxapyroxad, an emerging succinate dehydrogenase inhibitor fungicide, is widely used due to its excellent properties. Given its persistence in soil with a 50 % disappearance time of 183-1000 days, it is crucial to evaluate the long-term effects of low-dose fluxapyroxad on non-target soil organisms such as earthworms ( Eisenia fetida). The present study investigated the impacts of fluxapyroxad (0.01, 0.1, and 1 mg kg(-1 )) on Eisenia fetida over 56 days, focusing on oxidative stress, digestive and nervous system functions, and histopathological changes. We also explored the mechanisms of fluxapyroxad-enzyme interactions through molecular docking and dynamics simulations. Results demonstrated a significant dose-response relationship in the integrated biomarker response of 12 biochemical indices. Fluxapyroxad altered expression levels of functional genes and induced histopatho- logical damage in earthworm epidermis and intestines. Molecular simulations revealed that fluxapyroxad is directly bound to active sites of critical enzymes, potentially disrupting their structure and function. Even at low doses, long-term fluxapyroxad exposure significantly impacted earthworm physiology, with effects becoming more pronounced over time. Our findings provide crucial insights into the chronic toxicity of fluxapyroxad and emphasize the importance of long-term, low-dose studies in pesticide risk assessment in soil. This research offers valuable guidance for the responsible management and application of fungicides.

Salinity stress has become a major threat to worldwide crop production. Exogenous melatonin (MT) has appeared as a promising treatment against salt stress in several plant species. However, MT effect on the tolerance of sorghum plants under different saline conditions (moderate and severe) remains ambiguous. This study was carried out to explore the impact of MT (0, 50, 100 and 200 mu M) as a foliar application on sorghum seedlings grown under moderate and severe saline conditions using sodium chloride, NaCl (75 and 150 mu M NaCl). Salinity treatments were applied as solution in sand medium in pots. The results demonstrated that rising salinity level negatively affected plant growth, photosynthetic pigments (chlorophylls and carotenoids), leaf water status and ionic homeostasis (sodium, potassium, and calcium ions). Applied-MT specifically at 100 or 200 mu M enhanced the osmotic balance, cell membrane stabilizing and leaf relative water content. These effects were associated with an obvious restriction to the level of hydrogen peroxide, lipid peroxidation (malondialdehyde content) and methylglyoxal. Moreover, antioxidant activities of peroxidase, catalase, superoxide dismutase, and ascorbate peroxidase enzymes were modulated by MT treatments. Molecular docking modeling assessment illustrated top-ranked confirmations between MT and the target antioxidant enzymes. MT forms multiple hydrogen bonds with key amino acid residues for glycine (A: 162), tryptophan (A: 41), leucine (A: 165), tyrosine (A: 235) in the active site of ascorbate peroxidase. The alkyl interactions with leucine (A: 37), arginine (A: 38) and cysteine (A: 168) also contribute to its high affinity. Despite sorghum plant is commonly moderately tolerant to salinity stress, the results of this study confirmed its high sensitivity to a wide range of saline conditions at early growth stages. Melatonin spraying led to improvements in various morphological, physiological and biochemical mechanisms that harmonized together to confer stress resistance to salt-stressed sorghum seedlings.

Contact herbicides are widely used if rapid weeds eradication is required despite of a number of inherent disadvantages (transfer to water and soil, damage of non-target plants, promotion of resistant weeds expansion, etc.). Supramolecular chemistry can solve the problems associated with herbicide degradation and spreading, as well as suppress their harmful effects on humans and the environment. Pillar[n]arene derivatives are of special interest among other macrocyclic platforms due to their ability to implement various substrates in the macrocycle cavity. However, most of the works devoted to the interaction of pillararenes with pesticides considers binding of paraquat and its derivatives. In this work, water soluble derivatives of pillar[5]arene containing Ltryptophan residues have been proposed for binding a range of herbicides including paraquat dichloride, pyridate, 3-(methylphosphinico)propionic acid, and glufosinate-ammonium. The ester derivative of pillar[5]arene was found to be able to bind the above species. The betaine derivative showed selective and efficient interaction with pyridate (logKa = 4.02) and paraquat (logKa = 3.17). The effect of the charge of the pillar[5]arene substituent on the toxicity of the macrocyclic platform towards A549 and LEK cell lines was demonstrated. Introduction of carboxylate functions to form betaine fragments compensated for the positive charge of the macrocycle substituent and decreased its toxicity by three orders of magnitude for A549 cell line (167.0 mu M), and by two orders of magnitude for LEK cells (56.0 mu M) compared to ester derivative of pillar[5]arene (3.1 and 3.6 mu M respectively). The results obtained confirmed the prospects of the use of amino acid derivatized pillar[5] arenes in the development of new approaches to the removal of the herbicides from the environment that are demanded both in agriculture and aquaculture.

Pesticides are substances used for controlling, preventing, and repelling pests in agriculture. Among them, neonicotinoids have become the fastest -growing class of insecticides because of their efficiency in targeting pests. They work by strongly binding to nicotinic acetylcholine receptors (nAChRs) in the central nervous system of insects, leading to receptor blockage, paralysis, and death. Despite their selectivity for insects, these substances may be hazardous to non -target creatures, including earthworms. Although earthworms may be invasive in some regions like north America, they contribute to the development of soil structure, water management, nutrient cycling, pollution remediation, and cultural services, positively impacting the environment, particularly in the soil ecosystem. Thus, this study aimed to develop a novel earthworm behavior assay since behavior is a sensitive marker for toxicity assay, and demonstrated its application in evaluating the toxicity of various neonicotinoids. Here, we exposed Eisenia fetida to 1 and 10 ppb of eight neonicotinoids (acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram pestanal, thiacloprid, thiametoxam, and sulfoxaflor) for 3 days to observe their behavior toxicities. Overall, all of the neonicotinoids decreased their locomotion, showed by a reduction of average speed by 24.94 -68.63% and increment in freezing time movement ratio by 1.51 -4.25 times, and altered their movement orientation and complexity, indicated by the decrement in the fractal dimension value by 24 -70%. Moreover, some of the neonicotinoids, which were acetamiprid, dinotefuran, imidacloprid, nitenpyram, and sulfoxaflor, could even alter their exploratory behaviors, which was shown by the increment in the time spent in the center area value by 6.94 -12.99 times. Furthermore, based on the PCA and heatmap clustering results, thiametoxam was found as the neonicotinoid that possessed the least pronounced behavior toxicity effects among the tested pesticides since these neonicotinoid-treated groups in both concentrations were grouped in the same major cluster with the control group. Finally, molecular docking was also conducted to examine neonicotinoids ' possible binding mechanism to Acetylcholine Binding Protein (AChBP), which is responsible for neurotransmission. The molecular docking result confirmed that each of the neonicotinoids has a relatively high binding energy with AChBP, with the lowest binding energy was possessed by thiametoxam, which consistent with its relatively low behavior toxicities. Thus, these molecular docking results might hint at the possible mechanism behind the observed behavior alterations. To sum up, the present study demonstrated that all of the neonicotinoids altered the earthworm behaviors which might be due to their ability to bind with some specific neurotransmitters and the current findings give insights into the toxicities of neonicotinoids to the environment, especially animals in a soil ecosystem.