Peroxidation Levels Research Articles

Effect of Potassium Optimization on Wheat Drought Tolerance in Controlled Conditions

Potassium is an essential nutrient that influences key processes in plants, including osmotic regulation, photosynthesis, and nitrogen assimilation. This study investigated the drought tolerance of wheat (Triticum spp.) plants treated with sufficient potassium (SK, 1 mM) and low potassium (LK, 0.05 mM) under PEG-induced drought stress. Plant physiological development, canopy temperature, photosynthetic efficiency, antioxidant defense enzymes, and nitrogen assimilation enzymes were assessed. In non-drought conditions, LK increased canopy temperature and reduced dry matter yield and photosynthetic performance, with these effects becoming more pronounced under drought stress. SK-treated plants exhibited higher biomass, chlorophyll content, maximum quantum efficiency of photosystem II, and lower canopy temperatures, even under drought conditions. Furthermore, LK restricted the accumulation of key osmotic regulators, including proline, amino acids, and soluble sugars. Under drought stress, LK plants also showed increased hydrogen peroxide and superoxide anion levels, while SK plants had lower reactive oxygen species accumulation and higher antioxidant enzyme activities (catalase and superoxide dismutase). Additionally, LK resulted in reduced activity of nitrogen assimilation enzymes (nitrate reductase, NR, and nitrite reductase, NiR) under both normal and drought conditions. In contrast, SK-treated wheat seedlings maintained higher NR and NiR activities and higher soluble protein content during drought stress. These findings underscore the critical role of potassium management in enhancing wheat yield, particularly in water-scarce regions, as optimal potassium supply strengthens essential physiological and biochemical mechanisms that improve plant tolerance to drought stress.

Sulfur deficiency reduces the thermotolerance of Heliotropium thermophilum to high temperatures

Heliotropium thermophilum, a thermotolerant plant, was subjected to low sulfate treatments to examine the effects of sulfur deficiency on the plant's thermotolerance. For this aim, two different concentrations (0.15 mM and 0.30 mM) of low-sulfate media as well as full nutrition (FN) medium were prepared and the plants were cultured at 25 °C for 60 days, then divided into 2 groups for temperature applications and kept at either 25 or 40 °C for 7 days. H. thermophilum could survive in low-sulfate media at 40 °C, but high temperature damages such as chlorosis, and green color retention were observed. In addition, heat treatment reduced plant fresh weight, relative water content, and total sugar contents in both low-sulfate media. Moreover, proline and hydrogen peroxide levels were the highest in plants grown in 0.15 mM sulfate at 40 °C. Peroxidase activities were increased in plants grown in low-sulfate media at high temperature, compared to values at 25 °C. In plants grown in 0.30 mM sulfate medium, catalase activity was elevated, whereas it was reduced in 0.15 mM sulfate-grown plants at 40 °C compared to the values at 25 °C. Glutathione reductase (GR) activity at 40 °C was downregulated in 0.30 mM sulfate-grown plants while in those grown in FN and 0.15 mM-sulfate media it did not change. Heat Shock Factor 4 (HSF4) and HSFA4A genes were also upregulated by low sulfate and high temperature although HSFA4A gene activation was lower under sulfur deficiency. Moreover, HSFA3 gene expression at 40 °C decreased upon the application of 0.30 mM sulfate. We hypothesize that sulfur deficiency makes H. thermophilum susceptible to high temperatures by decreasing chlorophyll and sugar contents, and reducing the activities of the antioxidant enzymes and thus plant growth. Moreover, the down-regulation of the HSFA3 and HSFA4A gene, caused by sulfur deficiency, confirms the negative effects of sulfur deficiency on plant response to high temperatures.

Genome-Wide Identification of the GbUBC Gene Family in Sea-Island Cotton (Gossypium barbadense) and the Active Regulation of Drought Resistance in Cotton by GbUBC23

Cotton is an economically critical crop worldwide, and drought stress strongly affects its growth and development. Ubiquitination modifies protein activity and is crucial in numerous biological processes. Ubiquitin-conjugating enzymes serve as intermediaries in the protein ubiquitination process and play important roles in plant responses to abiotic stress. However, the impact of ubiquitination on the response of cotton to abiotic stress is not fully understood. Bioinformatic methods were employed in this study to analyze the physiochemical characteristics, gene structure, collinearity, expression patterns, and evolutionary relationships of GbUBC gene family members in sea-island cotton. In sea-island cotton, a minimum of 125 GbUBC genes are irregularly distributed across the 26 chromosomes, with multiple instances of gene duplication observed among the members. Phylogenetic analysis categorized the GbUBC gene family into 15 ubiquitin-conjugating enzyme (E2) subgroups, one ubiquitin E2 enzyme variant (UEV) subgroup, and one COP10 subgroup. GbUBC gene expression pattern analyses revealed that most GbUBC genes responded differently to cold, heat, NaCl, and polyethylene glycol (PEG) treatments, with certain GbUBC genes exhibiting high expression levels in specific fiber development period and organs. Furthermore, molecular biology methods were employed to elucidate the biological functions of GbUBC23. The GbUBC23 gene was highly expressed in the cotyledons of sea-island cotton and was activated by PEG treatment. GbUBC23 is localized to the nucleus and cytomembrane. The silencing of the GbUBC23 gene under drought conditions led to decreased drought tolerance and survival rates in sea-island cotton. Compared with those in the control plants, the activity of proline and superoxide dismutase and the expression levels of the drought-induced genes GbNCED3, GbRD22, GbRD26 were significantly lower, but the levels of malondialdehyde and hydrogen peroxide were significantly higher. Our findings revealed 125 members of the GbUBC gene family in sea-island cotton, with the GbUBC23 gene critically contributing to the abiotic stress response. These findings indicate that the GbUBC gene family may play a crucial role in the drought stress response in sea-island cotton.

Application of hydrogen-rich water maintains red pitaya fruit quality through regulation of ROS and energy metabolism

Hydrogen-rich water (HRW) treatment has been shown to enhance the shelf life of fruit and vegetables. This study aimed to investigate the effects of HRW on improving the quality of red pitaya and its underlying regulatory mechanisms. The results revealed that applying HRW at a 70% concentration reduced decay and weight loss rates, slowed the respiratory rate, and delayed the decline in titratable acidity and total soluble solids. Additionally, HRW treatment mitigated the increase in superoxide anion production and hydrogen peroxide levels, while enhancing antioxidant enzyme activities and gene expression, including those of peroxidase, superoxide dismutase, glutathione peroxidase, catalase, ascorbate peroxidase, monodehydroascorbate reductase, and glutathione reductase. Non-enzymatic antioxidant compounds such as ascorbate and glutathione also increased. Moreover, RT-qPCR analysis showed that HRW treatment upregulated HcMYB6 and downregulated HcR2R3MYB. Dual-luciferase reporter assays indicated that HcMYB6 activated the expression of HcSOD and HcCAT, whereas HcR2R3MYB repressed their expression. These findings suggest that HcMYB6 and HcR2R3MYB may be involved in reactive oxygen species metabolism, with HcMYB6 being induced and HcR2R3MYB inhibited by HRW treatment. Furthermore, HRW treatment led to increased adenosine triphosphate and adenosine diphosphate levels, a decrease in adenosine monophosphate content, and elevated gene expression and activity of Ca2⁺-ATPase, succinate hydrogenase, H⁺-ATPase, and cytochrome C. Collectively, these results demonstrate that HRW treatment effectively reduces oxidative damage and improves energy status, thereby preserving the quality of red pitaya fruit.

The paradoxical effects of beneficial bacteria on Solanum lycopersicum under Cd stress.

This study investigated the complex interactions between a novel consortium and tomato seedlings under cadmium (Cd) stress. The consortium consists of two bacteria, Pseudomonas sp. HS4 and Paenarthrobacter sp. AS8, both with proven plant growth-promoting (PGP) properties, isolated from Cd hyperaccumulators. Our research highlights the paradoxical effects of these bacteria, revealing their dual role in reducing Cd uptake while simultaneously inducing oxidative stress in plants. Hydroponic experiments showed that the consortium reduced Cd accumulation in tomato shoots by 52% compared to uninoculated controls. However, this reduction was accompanied by decreased plant biomass and increased oxidative stress, with malondialdehyde (MDA) and hydrogen peroxide (H₂O₂) levels up to 80% and 160% higher, respectively, in inoculated plants. Root H₂O₂ production increased by 38% under 50 μM Cd without a corresponding rise in catalase (CAT) activity. Despite Cd exposure, the consortium promoted chlorophyll and carotenoid synthesis, restoring pigment levels to those of unstressed controls. Gene expression analysis revealed a complex impact on stress responses, with inoculation suppressing Sl1 gene expression in roots and upregulating the oxidative stress-related GR-1 gene in shoots. These findings highlight the complex and multifaceted relationship between beneficial bacteria and plant fitness under heavy metal stress, with significant implications for sustainable agriculture. The study raises new questions regarding the broader physiological and ecological impacts of applying hyperaccumulator-associated bacteria in crop management, emphasizing the necessity for deeper mechanistic insights into these interactions to fully harness their potential in improving crop resilience and productivity.

Rapid changes in stress-related gene expression after short exposure of Arabidopsis leaves to cold plasma

Cold Atmospheric Plasma (CAP) technology has emerged as a promising tool in various biological applications due to its ability to generate a composite signal comprising reactive oxygen and nitrogen species, ultraviolet radiation, and electromagnetic fields, all while maintaining a stable temperature. Although CAP treatments have demonstrated significant effects on seed germination and plant growth, the direct molecular responses of plants to CAP exposure remain poorly understood. In this study, young Arabidopsis thaliana leaves were exposed to a brief 5- or 30-s localized CAP treatment, resulting in rapid and localized tissue damage without causing lethal effects on the entire plant. Molecular analyses conducted on the entire plant rosette revealed a notable increase in hydrogen peroxide levels, along with the upregulation of stress-related genes, akin to a wound response. Of particular interest, the activation of RelA/SpoT Homolog (RSH) genes encoding proteins that regulate the synthesis of the stress marker (p)ppGpp, also known as alarmone, and playing a major role in the energic regulation of photosynthesis, occurred shortly after CAP exposure. The expression of RSH genes was up-regulated after 5s CAP exposure, while the wound stress marker ZAT12 remained unaffected, highlighting a specific signalling pathway to activate RSH genes. This finding suggests the potential involvement of the alarmone signalling pathway in the plant's response to CAP exposure, thereby opening avenues for further exploration of metabolic pathways and signalling cascades induced by CAP treatment.

Andrographolide Attenuates Myocardial Ischemia-Reperfusion Injury in Mice by Up-Regulating PPAR-α.

Andrographolide (AGP), a bioactive diterpene lactone, is an active constituent extracted from Andrographis paniculata. It has many biological activities, such as antioxidant, antitumor, antivirus, anti-inflammation, hepatoprotection, and cardioprotection. The aim of the present study is to investigate the cardioprotective effects of AGP in a mouse model of myocardial ischemia-reperfusion injury (MIRI). Adult male C57BL/6J mice were pre-treated orally with AGP (25mg/kg) for six days. After 30min of the left anterior descending coronary artery occlusion followed by 24h of reperfusion, mice received an additional dose of AGP. The results showed that: (i) AGP pretreatment significantly reduced myocardial infarct size and cardiac injury biomarkers in MIRI mice and improved left ventricular ejection fraction (EF) and fractional shortening (FS); (ii) AGP pretreatment attenuated MIRI-induced oxidative stress imbalance in MIRI mice by increasing total antioxidant capacity (T-AOC) and reducing the levels of hydrogen peroxide (H2O2), nitric oxide (NO), malondialdehyde (MDA), and dihydroethidium (DHE); (iii) AGP pretreatment increased Bcl-2 expression and decreased caspase-3 and Bax expression in ischemic myocardial tissue, along with a reduction in TUNEL-positive cells. Further analysis showed that stimulation by I/R decreased peroxisome proliferator-activated receptor-α (PPAR-α) expression in ischemic cardiac tissue, which was prevented by AGP administration. Moreover, administration of the PPAR-α antagonist GW6471 (1mg/kg) abolished the protective effect of AGP on oxidative stress and apoptosis in the ischemic heart tissue of mice stimulated by ischemia-reperfusion. Taken together, these results suggest that AGP attenuates MIRI-induced cardiac injury by up-regulating PPAR-α expression, thereby preventing oxidative stress and cellular apoptosis.

Detecting structural and functional mitochondrial abnormalities in periodontal tissues using an experimental periodontitis model

Background: Recent research indicates that mitochondrial dysfunction plays a significant role in the development and progression of oral inflammation, such as periodontitis and pulpitis. Aim: To assess structural and functional mitochondrial abnormalities in periodontal tissues using an experimental periodontitis model in rats. Materials and methods: The study used male Wistar rats aged 4 months, with a body weight of 221.0±7.5 g. Simple randomization was used to divide the animals into two groups (n=10 each). Group 1 (control) consisted of intact animals, while Group 2 consisted of animals with experimentally induced periodontitis. A ligature-induced periodontitis model was used, with a non-absorbable polyfilament thread sutured into the gum near the mandibular incisors. Histological examinations were used to validate the experimental periodontitis model. The following molecular genetic and biochemical parameters were assessed: nuclear DNA and mitochondrial DNA (mtDNA) damage, abundance and heteroplasmy of mtDNA, mitochondrial gene expression, and levels of hydrogen peroxide (H2O2), malondialdehyde, and reduced glutathione. Results: The resulting experimental periodontitis model revealed histological changes in periodontal tissues, indicating periodontitis in the animals. On day 14 after ligation, histological findings showed that Group 2 had more significant mtDNA damage and heteroplasmy in periodontal tissues than Group 1 (control). Moreover, Group 2 showed a decrease in the expression of mtDNA genes involved in adenosine triphosphate synthesis. This group also had lower glutathione levels and higher H2O2 and malondialdehyde levels than the control group. Conclusion: The experimental periodontitis model in rats revealed structural and functional mitochondrial abnormalities in periodontal tissues. New approaches to assessing mitochondrial function in periodontitis may facilitate the diagnosis and treatment of the disease and its complications.

Translocation mechanism and the role of aerenchyma in nanoplastic translocation in Myriophyllum sp. "Roraima" and physiological responses.

Nanoplastics have become a growing concern due to their potential impact on freshwater vegetation. The uptake, translocation, and effects of 0.05-µm nanoplastics on Myriophyllum sp. "Roraima" were investigated, along with the role of aerenchyma in nanoplastic transport.Microscopic observations revealed nanoplastic particle adsorption to the plant surface and entry into the roots and stems, with higher abundance and more dispersed distribution by direct contact. Nanoplastic particles were detected in the plant stem, primarily concentrated in regions adjacent to the aerenchyma. No morphological effects were observed. Induced changes in photosynthesis, including increased maximum quantum efficiency of photosystem II (Fv/Fm), decreased non-photochemical quenching (NPQ), decreased photosynthetic pigments, and increased photoprotective pigments, were recognized. Additionally, hydrogen peroxide levels and antioxidant enzyme activities varied in response to nanoplastic exposure. This study provides insights into the impact of nanoplastics on Myriophyllum sp. "Roraima" and has reviewed the underlying mechanisms, highlighting the role of aerenchyma in nanoplastic transport within the plant. Moreover, this study contributes to the understanding of the potential impacts of nanoplastic pollution on freshwater macrophytes while acknowledging the influence of phyto-anatomical structure on nanoplastic translocation.

Divacancy graphene and graphyne as potential biomedical sensors: A first-principles study

Imbalance in the levels of hydrogen peroxide signals the onset of chronic diseases in our body. Thus, it becomes imperative to design simple material systems with single molecule sensitivity. In this study, we investigate graphene and graphyne based systems by including various vacancy structures to assess their potential as H2O2 sensor materials. From the computed adsorption energies, we select two promising candidates, interestingly both are divacancies in graphene and graphyne. We then investigate electron transport in both the systems using the DFT-NEGF approach. Upon adsorption of H2O2 on the 585 vacancy (a special case of divacancy) in graphene and divacancy graphyne monolayers, we observe distinguishing current-voltage and electron transmission characteristics, in particular, in the former. For the 585 divacancy graphene system through analysis of the electronic properties, we identify the underlying mechanisms responsible for the difference in current values between the clean and H2O2 adsorbed systems, and hence its sensing ability. This work opens up a new avenue of intelligently incorporating vacancy defects in cheaper carbon-based 2D materials to effectively serve as potentially highly sensitive and selective biosensors for early disease detection.

Nanoscale Mixed-Ligand Metal-Organic Framework for X-ray Stimulated Cancer Therapy.

Concurrent localized radiotherapy and systemic chemotherapy are standards of care for many cancers, but these treatment regimens cause severe adverse effects in many patients. Herein, we report the design of a mixed-ligand nanoscale metal-organic framework (nMOF) with the ability to simultaneously enhance radiotherapeutic effects and trigger the release of a potent chemotherapeutic under X-ray irradiation. We synthesized a new functional quaterphenyl dicarboxylate ligand conjugated with SN38 (H2QP-SN) via a hydroxyl radical-responsive covalent linkage. Because of the similar length of QP-SN and bis(p-benzoato)porphyrin (DBP) ligands, QP-SN was incorporated into Hf-DBP nMOF to afford a novel multifunctional mixed-ligand Hf-DBP-QP-SN nMOF with good biocompatibility. Hf-DBP-QP-SN not only enhances radiation damage to tumors via a unique radiotherapy-radiodynamic therapy (RT-RDT) process but also increases ·OH generation from radiolysis with electron-dense Hf12 secondary building units (SBUs) to release SN38 from Hf-DBP-QP-SN for chemotherapy. Elevated levels of hydrogen peroxide in the tumor microenvironment further stimulate the release of SN38 by enhancing ·OH generation under X-ray irradiation. With low doses of X-ray irradiation, Hf-DBP-QP-SN suppressed the growth of CT26 colon and 4T1 breast tumors by 93.5% and 95.2%, respectively, without any sign of general toxicity. Our study highlights the potential of using ionizing radiation-mediated chemistry for on-demand activation of nanotherapeutics for synergistic radiotherapy and chemotherapy without causing severe adverse effects.

Management of yield losses in Vigna radiata (L.) R. Wilczek crop caused by charcoal-rot disease through synergistic application of biochar and zinc oxide nanoparticles as boosting fertilizers and nanofungicides

The mung bean crop (Vigna radiata (L.) R. Wilczek) is widely recognized as a key source of pulse food worldwide. However, this crop suffers substantial yield losses due to humid environments, particularly from infestations by the fungal pathogen Macrophomina phaseolina, which causes charcoal rot disease. This infestation results in significant agronomic losses, affecting both the crop’s growth characteristics and overall yield. Previous research suggests that these losses can be mitigated through environmentally friendly soil amendments, such as biochar, as well as by applying various nanofungicides. This study aims to explore the potential of biochar and zinc oxide nanoparticles (ZnONPs) to reduce the severity of charcoal rot disease and enhance the agronomic traits and yield of mung bean plants affected by this disease. The experiment was conducted in triplicate, applying ZnONPs at three concentrations (5, 10, and 20 mg. L− 1) via foliar spraying, combined with two levels of biochar (20 g and 40 g per pot). Positive and negative control treatments were also included for comparison. The results demonstrated that applying 40 g of biochar per pot and 20 mg. L− 1 of foliar-applied ZnONPs increased the activities of the anti-oxidative defence enzymes. Additionally, this treatment strategy boosted the plants’ disease resistance mechanisms, leading to lower mortality rates and reduced levels of malondialdehyde (MDA) and hydrogen peroxide (H₂O₂) by 61.7% and 49.23%. Moreover, the treatment positively impacted key growth parameters, increasing total chlorophyll content by 43%, plant height by 47%, and legume count per plant by 80.4%. The application of biochar and ZnONPs also improved seed protein content, reflecting an enhancement in nutritional quality. This study supports the use of biochar and ZnONPs as biostimulants to manage yield losses in mung bean crops affected by charcoal rot disease. The future prospects of using ZnONPs and biochar as treatments in agriculture are promising, as they offer innovative, eco-friendly solutions to enhance crop productivity, improve soil health, and reduce reliance on synthetic chemicals, paving the way for more sustainable and resilient agricultural systems.

Comparative Analysis of Phytochemicals and Gene Expression in Soybean (Glycine max) Under Acute Moderated and Severe Elevated Ozone: Unravelling the Role of Antioxidant Defence

ABSTRACTThe increasing concentrations of ground‐level ozone (O3) resulting from industrialisation and anthropogenic activities present a substantial environmental threat to agricultural productivity, particularly affecting O3‐sensitive crops such as soybeans. The effects of acute O3 exposure on soybean yield attributes and seed quality and whether soybean showed different detoxification mechanisms in response to moderate and severe O3 stress are not extensively explored. In this study, soybean seedlings were exposed to moderate (80 nmol mol−1) and acute severe (200 nmol mol−1) O3 stress, and then growth parameters, yield attributes, reactive oxygen species (ROS) levels, enzymatic and non‐enzymatic antioxidant properties and associated gene expression in the leaves were assessed. The results revealed that moderate O3 exposure enhanced growth parameters but reduced the 100‐grain weight, while acute severe exposure sharply depressed growth parameters, yield attributes and the 100‐grain weight. Moderate O3 fumigation significantly increased hydrogen peroxide (H2O2) levels and catalase (CAT) activity from 4 to 32 h. Acute severe O3 stress induced the overproduction of superoxide anions (O2.−) and H2O2 during nearly the whole experiment period, but only enhanced superoxide dismutase (SOD) activity at 32 h, and showed no stimulatory effects on CAT activity. Additionally, the relative expression levels of the SOD and CAT gene family in soybean leaves exposed to elevated O3 were upregulated, peaking at 8 h. Moderate O3 treatment enhanced reduced glutathione (GSH) and ascorbate (AsA) levels and increased the activities of AsA–GSH cycle‐related enzymes. In contrast, acute severe O3 exposure inhibited GSH and AsA contents and markedly suppressed AsA–GSH cycle‐related enzymes, particularly from 8 to 32 h. Redundancy analysis indicated that CAT and AsA play crucial roles in scavenging O3‐induced ROS under moderate stress, while ascorbate peroxidase (APX) and GSH were more effective under acute severe stress conditions. These findings provide insights into the differential impacts of acute O3 stress on soybeans, emphasising the importance of considering both crop yield and grain quality in assessing O3 risks to crops.

Orf116b Induces Pollen Abortion in a Novel Cotton (Gossypium hirsutum L.) Cytoplasmic Male Sterile Line J4A.

Cytoplasmic male sterile (CMS) systems have great potential in hybrid seed production in many plants. However, the incompatibility between the cytoplasmic and nuclear genes and the availability of fewer CMS lines limit the system's application in cotton heterosis. Therefore, the present study sequenced the mitochondrial (mt) genomes of a novel cotton (Gossypium hirsutum L.) CMS line J4A and its cytoplasmic nuclear homologous maintainer line J4B to investigate the mechanism underlying CMS and improve its application. A novel CMS gene, orf116b, was identified in the CMS line. Ectopic expression of orf116b in Escherichia coli suppressed growth, while its overexpression in Arabidopsis, rice, tobacco, and cotton led to complete or partial male sterility. Further analysis of anthers revealed mt disruption in J4A with higher levels of hydrogen peroxide (H2O2) and malondialdehyde (MDA), but lower levels of ATP and ribosomal protein (RP) than in J4B. Finally, a membrane-based yeast two-hybrid (MYTH) assay and bimolecular fluorescence complementation (BiFC) assays demonstrated that orf116b probably interacts with an anther-specific protein, LAT52. These observations collectively proved that orf116b is associated with early and stable pollen abortion in cotton, providing a foundation for further research on cotton fertility restoration and heterosis breeding.

Genome-wide analysis of miR172-mediated response to heavy metal stress in chickpea (Cicer arietinum L.): physiological, biochemical, and molecular insights

BackgroundChickpea (Cicer arietinum L.), a critical diploid legume in the Fabaceae family, is a rich source of protein, vitamins, and minerals. However, heavy metal toxicity severely affects its growth, yield, and quality. MicroRNAs (miRNAs) play a crucial role in regulating plant responses to both abiotic and biotic stress, including heavy metal exposure, by suppressing the expression of target genes. Plants respond to heavy metal stress through miRNA-mediated regulatory mechanisms at multiple physiological, biochemical, and molecular levels. Although the Fabaceae family is well represented in miRNA studies, chickpeas have been notably underrepresented. This study aimed to investigate the effects of heavy metal-induced stress, particularly from 100 µM concentrations of cadmium (Cd), chromium (Cr), nickel (Ni), lead (Pb), and 30 µM arsenic (As), on two chickpea varieties: ILC 482 (sensitive) and Azkan (tolerant). The assessment focused on physiological, biochemical, and molecular parameters. Furthermore, a systematic characterization of the miR172 gene family in the chickpea genome was conducted to better understand the plant’s molecular response to heavy metal stress.ResultsVariance analysis indicated significant effects of genotype (G), treatment (T), and genotype-by-treatment (GxT) interactions on plant growth, physiological, and biochemical parameters. Heavy metal stress negatively impacted plant growth in chickpea genotypes ILC 482 and Azkan. A reduction in chlorophyll content and relative leaf water content was observed, along with increased cell membrane damage. In ILC 482, the highest hydrogen peroxide (H₂O₂) levels in shoot tissue were recorded under As, Cd, and Ni treatments, while in Azkan, peak levels were observed with Pb treatment. Malondialdehyde (MDA) levels in root tissue were highest in ILC 482 under Cd and Ni exposure and in Azkan under As, Cr, and Cd treatments. Antioxidant enzyme activities, including superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), and ascorbate peroxidase (APX), were significantly elevated under heavy metal stress in both genotypes. Gene expression analysis revealed upregulation of essential antioxidant enzyme genes, such as SOD, CAT, and APX, with APX showing notable increases in both shoot and root tissues compared to the control. Additionally, seven miR172 genes (miR172a, miR172b, miR172c, miR172d, miR172e, miR172f, and miR172g) were identified in the chickpea genome, distributed across five chromosomes. All genes exhibited conserved hairpin structures essential for miRNA functionality. Phylogenetic analysis grouped these miR172 genes into three clades, suggesting strong evolutionary conservation with other plant species. The expression analysis of miR172 and its target genes under heavy metal stress showed varied expression patterns, indicating their role in enhancing heavy metal tolerance in chickpea.ConclusionsHeavy metal stress significantly impaired plant growth and physiological and biochemical parameters in chickpea genotypes, except for cell membrane damage. The findings underscore the critical role of miR172 and its target genes in modulating chickpea’s response to heavy metal stress. These insights provide a foundational understanding for developing stress-tolerant chickpea varieties through miRNA-based genetic engineering approaches.

Unraveling the acute sublethal effects of acetamiprid on honey bee neurological redox equilibrium

Understanding the off-target effects of neonicotinoid insecticides, including acetamiprid, which is the most commonly applied agricultural chemical, is crucial as it may be an important factor of negative impact on pollinator insects causing a number of problems such as colony collapse disorder (CCD) of honey bees. While CCD is known as a multifactorial disease, the role of pesticides in this context is not negligible. Therefore, it is essential to gain a deeper comprehension of the mechanisms through which they function. The aim of this research was to study the effects of sublethal acetamiprid doses on honey bees, specifically focusing on the redox homeostasis of the brain. According to our findings, it can be confirmed that acetamiprid detrimentally impacts the redox balance of the brain increasing hydrogen peroxide and malondialdehyde levels, suggesting consequential lipid peroxidation and membrane damage as consequences. Moreover, acetamiprid had negative effects on the glutathione system and total antioxidant capacity, as well as key enzymes involved in the maintenance of redox homeostasis. In summary, it can be concluded that acetamiprid adversely affected the redox balance of the central nervous system of honey bees in our study. Our findings could potentially contribute to a better understanding of pesticide-related consequences and to improvement of bee health.

Effects of Deltamethrin on Photosynthetic Pigments and Ascorbate-Glutathione (ASA-GSH) Cycle in Lemna minor

Deltamethrin is a synthetic pyrethroid insecticide that can cause adverse effects on non-target organisms. This study was designed to investigate the effects of different concentrations (0.001, 0.005 and 0.01 ppm) of deltamethrin on photosynthetic pigments and the ascorbate-glutathione (ASA-GSH) cycle in Lemna minor, a freshwater macrophyte. To assess the effect of deltamethrin on L. minor, photosynthetic pigments, malondialdehyde (MDA) and hydrogen peroxide (H2O2) levels, and the activities of some antioxidant enzymes (SOD, CAT and POD) and enzymatic and non-enzymatic antioxidants associated with the ASA-GSH cycle were measured. The results showed that exposure to deltamethrin decreased chl a, chl b and carotenoid levels and increased MDA and H2O2 levels. In addition, deltamethrin exposure significantly increased SOD, CAT and POD activities. The activities of ASA-GSH cycle enzymes (APX, GR, GPX, MDHAR and DHAR) decreased in L. minor exposed to 0.01 ppm deltamethrin, while GST activity increased. Exposure to low doses of deltamethrin increased ASA and GSH levels, while 0.01 ppm deltamethrin decreased the amounts of ASA and GSH compared to the control. Taken together, the present study revealed that different concentrations of deltamethrin inhibited photosynthetic activity, increased lipid peroxidation and caused oxidative stress and activated the antioxidant defense system of L. minor to eliminate the increased oxidative stress.

Unveiling Salt Tolerance Mechanisms and Hub Genes in Alfalfa (Medicago sativa L.) Through Transcriptomic and WGCNA Analysis.

Alfalfa (Medicago sativa L.), an important forage crop with high nutritional value and good palatability, plays a vital role in the development of animal husbandry in China. In Northeast China, there are vast areas of saline-alkali land that remain undeveloped. Given that alfalfa is a highly adaptable forage crop, exploring its salt tolerance at the molecular transcriptional level and identifying salt-tolerant genes has great significance for breeding salt-resistant alfalfa varieties. This also provides valuable genetic resources for better utilization of saline-alkali land. In this study, we conducted two rounds of screening on 41 alfalfa varieties and identified WL168 as a salt-sensitive variety and Longmu801 as a salt-tolerant variety. After 7 days of 300 mM salt stress, both varieties showed a decreasing trend in plant height, fresh weight, and dry weight over time, but Longmu801 demonstrated better water retention ability compared to WL168. Chlorophyll content also declined, but chlorophyll a and total chlorophyll levels in Longmu801 were higher than in WL168. Hydrogen peroxide and malondialdehyde levels increased overall, but Longmu801 had significantly lower levels than WL168 under prolonged stress. Both varieties showed increasing trends in soluble sugars, proline, and antioxidant enzymes (SOD, POD, CAT), with Longmu801 significantly outperforming WL168. This suggests that the two varieties share similar growth and physiological response mechanisms, with their differences primarily arising from variations in indicator levels. In the above, comparisons between varieties were conducted based on the relative values of the indicators in relation to their controls. Transcriptomic analysis revealed that under salt stress, Longmu801 had 16,485 differentially expressed genes (DEGs) relative to its control, while WL168 had 18,726 DEGs compared to its control. Among these, 2164 DEGs shared the same expression trend, with GO functions enriched in response to oxidative stress, nucleus, plasma membrane, and others. The KEGG pathways were enriched in phenylpropanoid biosynthesis, protein processing in the endoplasmic reticulum, starch and sucrose metabolism, and others. This suggests that alfalfa's transcriptional response mechanism to salt stress involves these pathways. Additionally, the variety-specific DEGs were also enriched in the same KEGG pathways and GO functions, indicating that the differences between the two varieties stem from their unique stress-responsive DEGs, while their overall mechanisms for coping with stress remain similar. To further identify salt stress-related genes, this study conducted WGCNA analysis using 32,683 genes and physiological indicators. Six modules closely related to physiological traits were identified, and the top five genes ranked by degree in each module were selected as hub genes. Further analysis of these hub genes identified five genes directly related to salt stress: Msa085011, Msa0605650, Msa0397400, Msa1258740, and Msa0958830. Mantel test analysis revealed that these genes showed strong correlations with physiological indicators. This study will provide important insights for breeding salt-tolerant alfalfa varieties.

Impact of organic, conventional, and stingless bee honeys on the antibacterial activity of gummy candies against oral bacteria

ObjectivesThis study aimed to investigate the impact of organic, conventional, and stingless honey on gummy candies, focusing on the effect of the cariogenic bacterium, Streptococcus mutans UA159, and total bacterial count in saliva from adolescents. MethodsAntimicrobial compounds in three honey samples were identified, and the minimum inhibitory concentration against S. mutans UA159 was determined. The antibacterial activities of the three honey candy formulations were determined against S. mutans UA159 in artificial saliva and total bacteria in saliva collected from adolescents. The sensory acceptance of the candy formulations by children, adolescents, and adults was investigated. ResultsCandies prepared using conventional honey showed the highest antibacterial activity against S. mutans UA159 in vitro and total bacteria in human saliva. This effect was attributed to the higher levels of quercetin, myricetin, caffeine, and hydrogen peroxide in conventional honey. ConclusionsNicotinic, ferulic, and p-coumaric acids found in honey had low antibacterial activity against oral bacteria. Quercetin, myricetin, caffeine, and hydrogen peroxide are the main anticariogenic compounds in honey and exert antibacterial effects on adolescent saliva, despite added to candies. However, organic production does not necessarily improve the biological properties of honey. All candies were equally liked by sensory assessors (acceptance >70%), facilitating the selection of honey with higher biological activities to formulate functional candies.

Modulatory effects of glutamic acid on growth, photosynthetic pigments, and stress responses in olive plants subjected to cadmium stress

Cadmium (Cd) is a toxic heavy metal that severely impacts plant growth and photosynthesis and induces oxidative stress. This study investigates the modulatory effects of glutamic acid (GA) on Olea europaea (olive) seedlings subjected to cadmium stress. The experiment included control, Cd-stressed, GA-treated, and combined Cd and GA-treated groups. Cd exposure significantly reduced plant growth, as evidenced by decreased root length (3.5 cm) and shoot length (9 cm) compared to control plants (5 cm and 12 cm, respectively). Additionally, Cd stress led to a reduction in chlorophyll content (16.2 mg/g fresh weight) and elevated oxidative markers like H2O2 and MDA. The application of GA significantly improved plant growth and physiological parameters, with statistically significant increases in root length (up to 6.5 cm) and shoot length (up to 14 cm) in the combined treatment group (p ≤ 0.05). Furthermore, GA treatment led to a marked elevation in total chlorophyll content (up to 27.5 mg/g fresh weight), compared to 16.2 mg/g in Cd-stressed plants (p ≤ 0.05), reflecting a significant improvement in photosynthetic efficiency. GA also elevated the antioxidant enzyme activity catalase (CAT) and peroxidase (POD), reducing oxidative stress by decreasing hydrogen peroxide and MDA levels. The findings suggest that glutamic acid effectively mitigates Cd-induced phytotoxicity, enhancing stress resistance and promoting plant growth. This research provides valuable insights into using glutamic acid as a possible approach to mitigate heavy metal stress in plants, offering implications for agriculture and environmental management in Cd-contaminated areas. Specific applications may include its use in phytoremediation practices or as a supplement in agricultural management to improve crop resilience in polluted environments. Further research could explore the molecular mechanisms underlying GA’s protective effects and its potential synergy with other biostimulants to enhance heavy metal tolerance in a broader range of crops.