Effect of silicon on the young maize plants exposed to nickel stress.

Nickel (Ni) is involved in several physiological processes in plants but its excess in environment has many phytotoxic effects. Silicon (Si), an element required for optimal plant performance, has been shown to have beneficial effects for plants coping with various types of stresses. Here we studied the alleviative potential of Si (2.5 mM) added to hydroponically grown maize (Zea mays L.) plants under Ni (100 µM) stress. Ni decreased most of the growth parameters, total chlorophyll (Chl) and leaf relative water content (RWC), and catalase (CAT; EC 1.11.1.6) activity, while leaf water loss (LWL), contents of proline (Pro), hydrogen peroxide (H2O2) and ascorbate (AsA), membrane lipid peroxidation and activities of peroxidase (POX; EC 1.11.1.7) and superoxide dismutase (SOD; EC 1.15.1.1) were increased. Supplementation of Si to Ni-treated plants enhanced the leaf area, Chl content, RWC, CAT and POX (only in younger leaf) activities and decreased LWL, the contents of Pro (in younger leaf), H2O2 (roots) and AsA, lipid peroxidation and POX and SOD activities. We may conclude that Si mitigated the Ni-induced stress in maize by amelioration of the leaf water deficient status (Pro, RWC, LWL), enhancing membrane stability (MDA) and influencing enzymatic (SOD, POX, CAT) and non-enzymatic (Pro, AsA) defence systems. The increased Chl content and leaf area improve overall plant performance.

Multiple effects of silicon on alleviation of nickel toxicity in young maize roots.

Although beneficial metalloid silicon (Si) has been shown to alleviate the toxicity of various heavy metals, there is a lack of knowledge about the role of Si in possible alleviation of phytotoxicity caused by excess of essential nickel (Ni). In the present study we investigated the growth and biomass production, reactive oxygen species (ROS) formation and activities of selected antioxidants, as well as combined effect of Ni and Si on the integrity of cell membranes and electrolyte leakage in young maize roots treated for 24, 48 and 72 h with excess of Ni and/or Si. By histochemical methods we also visualized Ni distribution in root tissues and compared the uptake of Ni and Si with the development of root apoplasmic barriers. Ni enhanced the root lignification and suberization and shifted the development of apoplasmic barriers towards the root tip. Similarly, localization of Ni correlated with lignin and suberin deposition in root endodermis, further supporting the barrier role of this tissue in Ni uptake. Si reversed the negative impact of Ni on root anatomy. Additionally, improved cell membrane integrity, and enhanced ascorbate-based antioxidant system might be the mechanisms how Si partially mitigates the deleterious effects of Ni excess in maize plants.

The effect of cadmium-nickel interactions on superoxide production, cell viability and membrane potential (EM) in roots of two maize cultivars.

Effects of CdCl2, NiCl2 or both on superoxide production, viability and membrane potential (EM) of root cells in meristematic (MZ) and differentiation (DZ) zones of two maize cultivars (cv. Premia and cv. Blitz) were studied. Plants were supplied with 10 and 100 µM concentrations of heavy metals (HM). The responses in the studied parameters to HM were concentration- and time-dependent, and were found only in the cells of MZ. The treatment of roots with Cd-stimulated massive superoxide production, although to different extent depending on the cultivar, root zone, and metal concentration. The stimulating effect of Ni on oxidative burst in Cd-treated maize roots was related to an increased Cd-induced superoxide production. The cell death appeared between 24 and 48 h and between 12 and 24 h of the 10 µM and 100 µM metal treatments, respectively. This was in accordance with Cd-induced ROS (superoxide) production and the EM decline in the corresponding time periods. Cell viability, EM changes and partially superoxide production indicate that the impact of the metals on the studied parameters declined in the order Cd+Ni > Cd > Ni and that cv. Blitz tends to respond more sensitively than cv. Premia.

Partially resistant Cucurbita pepo showed late onset of the Zucchini yellow mosaic virus infection due to rapid activation of defense mechanisms as compared to susceptible cultivar.

Zucchini yellow mosaic virus (ZYMV) is an emerging viral pathogen in cucurbit-growing areas wordwide. Infection causes significant yield losses in several species of the family Cucurbitaceae. To identify proteins potentially involved with resistance toward infection by the severe ZYMV-H isolate, two Cucurbita pepo cultivars (Zelena susceptible and Jaguar partially resistant) were analyzed using a two-dimensional gel electrophoresis-based proteomic approach. Initial symptoms on leaves (clearing veins) developed 6-7 days post-inoculation (dpi) in the susceptible C. pepo cv. Zelena. In contrast, similar symptoms appeared on the leaves of partially resistant C. pepo cv. Jaguar only after 15 dpi. This finding was confirmed by immune-blot analysis which showed higher levels of viral proteins at 6 dpi in the susceptible cultivar. Leaf proteome analyses revealed 28 and 31 spots differentially abundant between cultivars at 6 and 15 dpi, respectively. The variance early in infection can be attributed to a rapid activation of proteins involved with redox homeostasis in the partially resistant cultivar. Changes in the proteome of the susceptible cultivar are related to the cytoskeleton and photosynthesis.

Expression of P-glycoprotein in L1210 cells is linked with rise in sensitivity to Ca2+.

L1210/VCR cell line (R) was obtained by adaptation of the L1210 mouse leukaemia cells (S) to vincristine and showed P-glycoprotein (P-gp) mediated multidrug resistance (MDR). R cells were observed to be more sensitive to high external calcium as parental S. More pronounced calcium uptake was observed for R cells. Moreover, differences in intracellular calcium cell localization between S and R cells were found ultrastructurally following a calcium precipitating cytochemical method. In S cells, calcium precipitates were found to be localized predominantly along the cell surface coat and within mitochondria delineating the cristae. In R cells, precipitates were also found inside nuclei, at the border of heterochromatin clumps, and scattered within the cytoplasm. High extracellular calcium did not influence the P-gp mediated extrusion of calcein/AM as P-gp substrate. These results indicate that calcium enters and consequently damages the MDR cells to a higher extent than parental cells.