Asbestos is an industrially important microfiber present in cement industries and some mining sites and is very toxic to plant growth and development, but it has been neglected over the years. Therefore, this study was conducted to investigate the hazardous effects of asbestos on the growth and development of two important grass species (switchgrass and timothy grass). In order to mitigate the toxic effects of asbestos, a compost (bio-fertilizer) was also used. The asbestos soil samples were collected within a 10 km area of a cement factory. The results revealed that the asbestos-contaminated soils displayed a considerable increment in heavy metal uptake including chromium (Cr), manganese (Mn), vanadium (V), arsenic (As), and barium (Ba), which led to stunted plant growth. Consequently, the activities of antioxidant enzymes such as superoxide dismutase (SOD), glutathione peroxidase (GPX), and catalase (CAT) were stimulated to kept the redox balance under control. Among all the contaminated soils, the soil that was taken within a 0 Km area, closest to the cement factory, was the most toxic one. However, a compost amendment (25%) as a bio-fertilizer substantially reduced the toxic effects of asbestos fiber on the overall growth and development of plants, by reducing the metals’ uptake. Moreover, it was found that the roots of both grass species experienced higher heavy metal accumulation relative to the shoots. Collectively, it can be proposed that the studied grass species can be used for phytoextraction purposes, since both of them absorbed the heavy metals from the asbestos-contaminated soils.

Plant defence responses can be triggered by the application of elicitors for example chitosan (β-1,4-linked glucosamine; CHT). It is well-known that CHT induces rapid, local production of reactive oxygen species (ROS) and nitric oxide (NO) resulting in fast stomatal closure. Systemic defence responses are based primarily on phytohormones such as ethylene (ET) and salicylic acid (SA), moreover on the expression of hormone-mediated defence genes and proteins. At the same time, these responses can be dependent also on external factors, such as light but its role was less-investigated. Based on our result in intact tomato plants (Solanum lycopersicum L.), CHT treatment not only induced significant ET emission and stomatal closure locally but also promoted significant production of superoxide which was also detectable in the distal, systemic leaves. However, these changes in ET and superoxide accumulation were detected only in wild type (WT) plants kept in light and were inhibited under darkness as well as in ET receptor Never ripe (Nr) mutants suggesting pivotal importance of ET and light in inducing resistance both locally and systemically upon CHT. Interestingly, CHT-induced NO production was mostly independent of ET or light. At the same time, expression of Pathogenesis-related 3 (PR3) was increased locally in both genotypes in the light and in WT leaves under darkness. This was also observed in distal leaves of WT plants. The CHT-induced endoplasmic reticulum (ER) stress, as well as unfolded protein response (UPR) were examined for the first time, via analysis of the lumenal binding protein (BiP). Whereas local expression of BiP was not dependent on the availability of light or ET, systemically it was mediated by ET.

The mycotoxin fusaric acid (FA) induces rapid oxidative burst leading to cell death in plants. At the same time, plant defence reactions are mediated by several phytohormones for instance ethylene (ET). However, previously conducted studies leave research gaps on how ET plays a regulatory role under mycotoxin exposure. Therefore, this study aims to the time-dependent effects of two FA concentrations (0.1 mM and 1 mM) were explored on the regulation of reactive oxygen species (ROS) in leaves of wild-type (WT) and ET receptor mutant Never ripe (Nr) tomatoes. FA induced superoxide and H₂O₂ accumulation in both genotypes in a mycotoxin dose- and exposure time-dependent pattern. 1 mM FA activated NADPH oxidase (+34% compared to the control) and RBOH1 transcript levels in WT leaves. However, superoxide production was significantly higher in Nr with 62% which could contribute to higher lipid peroxidation in this genotype. In parallel, the antioxidative defence mechanisms were also activated. Both peroxidase and superoxide dismutase activities were lower in Nr but ascorbate peroxidase showed one-fold higher activity under 1 mM FA stress than in WT leaves. Interestingly, catalase (CAT) activity decreased upon FA in a time- and concentration-dependent manner and the encoding CAT genes were also downregulated, especially in Nr leaves at 20%. Ascorbate level was decreased and glutathione remained lower in Nr than WT plants under FA exposure. Conclusively, Nr genotype showed more sensitivity to FA-induced ROS suggesting that ET serves defence reactions of plants by activating several enzymatic and non-enzymatic antioxidants to detoxify excess ROS accumulation.

Fusarium pathogens are causal agents of several crop diseases and produce harmful mycotoxins resulting in crop and yield reduction worldwide. Among crop diseases, Fusarium wilt, Fusarium head blight, and Fusarium root blight are mostly reported diseases in numerous vegetables, crops, and fruits and have posed pressure on current food production and safety. In addition, the production of mycotoxins further aggravates plant health and causes serious health risks in humans and animals through food chain contamination. Different management practices have been enlisted in this chapter to reduce or eradicate Fusarium wilt in different crops. Interestingly, various mechanisms developed by plants have also been highlighted to fight against Fusarium pathogens and limit the growth of mycotoxins. One of defence mechanisms is plant antioxidant mechanisms to reduce oxidative stress by increasing enzymatic and non-enzymatic antioxidants to maintain cellular homeostasis under Fusarium infection. The other defence response is through hormonal signalling to combat fungal pathogens. Different phytohormones such as salicylic acid, ethylene, jasmonate, abscisic acid, cytokinin, auxin, and other plant secondary metabolites play a crucial part in the reduction of Fusarium growth and inhibit mycotoxin production through defence-related genes. Further, the use of different pre-harvest and post-harvest strategies has been elucidated to enhance plant resistance and growth by decreasing fungal pathogenicity and virulence.