In plants dehydration imposed by salinity can invoke physical changes at the interface of the plasma membrane and cell wall. Changes in hydrostatic pressure activate ion channels and cause depolarization of the plasma membrane due to disturbance in ion transport. During the initial phases of salinity stress, the relatively high osmotic potential of the rhizosphere enforces the plant to use a diverse spectrum of strategies to optimize water and nutrient uptake. Signals of salt stress are recognized by specific root receptors that activate an osmosensing network. Plant response to hyperosmotic tension is closely linked to the calcium (Ca2+) channels and interacting proteins such as calmodulin. A rapid rise in cytosolic Ca2+ levels occurs within seconds of exposure to salt stress. Plants employ multiple sensors and signaling components to sense and respond to salinity stress, of which most are closely related to Ca2+ sensing and signaling. Several tolerance strategies such as osmoprotectant accumulation, antioxidant boosting, polyaminses and nitric oxide (NO) machineries are also coordinated by Ca2+ signaling. Substantial research has been done to discover the salt stress pathway and tolerance mechanism in plants, resulting in new insights into the perception of salt stress and the downstream signaling that happens in response. Nevertheless, the role of multifunctional components such as Ca2+ has not been sufficiently addressed in the context of salt stress. In this review, we elaborate that the salt tolerance signaling pathway converges with Ca2+ signaling in diverse pathways. We summarize knowledge related to different dimensions of salt stress signaling pathways in the cell by emphasizing the administrative role of Ca2+ signaling on salt perception, signaling, gene expression, ion homeostasis and adaptive responses.
17 October 2019 in Journal of Plant Growth Regulation
Cadmium (Cd) is a heavy metal that is widely contaminating the environment due to its uses in industries as corrosive reagents, paints, batteries, etc. Cd can easily be absorbed through plant roots and may have serious negative impacts on plant growth. To investigate the mechanisms utilized by plants to cope with Cd toxicity, an experiment was conducted on maize seedlings. We observed that the plant growth and photosynthetic mechanism were negatively influenced during 20 days of Cd stress. The expression levels of ornithine decarboxylase (ORDC) increased in the six seedlings under Cd exposure compared to the control. However, Cd toxicity led to an increase in putrescine (Put) content only on day 15 when compared to the control plants. In fact, with the exception of day 15, the increases in the ORDC transcript levels did not show a direct correlation with the observed increases in Put content. Spermidine and Spermine levels were reduced on day 6 by Cd application, which was parallel with suppressed Spermidine synthase gene. However, an increase in Spermidine and Spermine levels was observed on day 12 along with a significant elevation in Spermidine synthase expression. On day 6, Cd was observed to start accumulating in the root with an increase in the expression of microRNA 528; while on day 15, Cd started to be observed in the shoot part with an increase in microRNA 390 and microRNA 168. These results imply that different miRNAs may regulate polyamines (PAs) in maize under Cd toxicity, suggesting a plant-derived strategy to commit a PAs/miRNA-regulated mechanism/s in different developmental stages (time points) in response to Cd exposure.
Cadmium (Cd) contamination is a critical environmental issue, adversely affecting plant growth and agricultural productivity. While numerous studies have explored the role of various bacteria in mitigating heavy metal toxicity, the specific impacts of sulfate-reducing bacteria ( Desulfovibrio desulfuricans, SRB) and the cyanobacterium Spirulina (Arthrospira platensis, SP), both individually and in combination, on Cd-contaminated plants remain underexplored. This study investigates the effects of SRB and SP on lettuce plants exposed to Cd contamination, aiming to enhance our understanding of their potential in alleviating Cd toxicity and promoting plant health. Results revealed that Cd contamination significantly reduced root growth in all treatments except for the combined application of SRB and SP. This combination also led to a marked decrease in leaf Cd content and improved leaf area, particularly under Cd stress. Furthermore, SP and SRB together increased the relative water content in contaminated soils, and SRB alone induced hydrogen peroxide production in non-contaminated soils. The co-application of SRB and SP significantly boosted catalase and superoxide dismutase activities, enhancing photosynthetic capacity and overall plant growth under Cd stress. These findings underscore the promising potential of using SRB and SP synergistically to mitigate Cd-induced challenges in lettuce cultivation, offering a viable strategy to improve crop productivity in contaminated environments.
Drought stress hinders plant growth by reducing water availability, leading to stunted plants growth, lower photosynthesis rates, and decreased yields. This research explored the impact of the combination of Spirulina and sulfate-reducing bacteria on the growth and resilience of lettuce plants under three drought levels (80%, 60%, and 40%). Overall, drought reduced germination percentages, but at 40% level, Spirulina significantly improved germination rates. At higher drought levels, Spirulina and sulfate-reducing bacteria positively influenced germination compared to the control, with SRB showing the most pronounced effect. Root growth increased significantly under 60% drought, though no root elongation under different stress levels was impacted. Leaf area decreased with increasing drought, but sulfate-reducing bacteria significantly enhanced it, especially at 80% drought. Control plants’ relative water content decreased with increasing drought severity. However, the combination of Spirulina and sulfate-reducing bacteria at 60% drought mitigated this effect. Notably, under 60% and 80% drought, hydrogen peroxide levels increased, though the Spirulina and sulfate-reducing bacteria combined consistently elevated hydrogen peroxide levels in both 60% and 80% conditions. Superoxide dismutase activity rose by 80% in non-treated plants, while Spirulina and sulfate-reducing bacteria individually enhanced superoxide dismutase activity across moderate and high drought. Catalase activity decreased at 80% drought in control plants; however, an increase was observed with sulfate-reducing bacteria in 80% stress level. The Fv/Fm ratio and PiABS declined as drought intensified, but sulfate-reducing bacteria improved these parameters at both 60% and 80% stress levels. ABS/RC and ET0/RC ratios responded positively to sulfate-reducing bacteria under severe drought. These findings suggest that while Spirulina and sulfate-reducing bacteria enhance drought tolerance in lettuce, sulfate-reducing bacteria are especially effective under higher drought stress conditions.
Soil salinity gradually become a major problem in arid and semi-arid regions of the world. Seed coating through bio-materials is a new method that maintains humidity around the seed. The aim of this study is to use absorbing bio-compounds to increase the percentage of germination and improving growth of Zea mays L. under salt stress. The experiment was conducted with maize seed which coated with tragacanth, tragacanth + Anabaena and tragacanth + Pseudo anabaena when exposed to 0, 120 and 160 mM NaCl per kg of coco-peat. All seed treatments effectively promoted seed germination percentage in 160 mM NaCl. Seed coating with tragacanth led to a significant increase of growth indices compared to the non-coated seeds under salt stress. While, the combination of tragacanth with Anabaena or Peusodoanabaena reduced the growth parameters. Coating treatment of maize seeds resulted in decreasing of Na content in the plants compared to the plants from non-coated seeds. The results suggested that maize seed coating with tragacanth could improve Na tolerance in the plants associated with a positive regulation of the seed germination and plant growth.