FON can infect and induce symptoms in watermelon plants at any growth stage

In the following section, we categorized those metabolites into five groups: amino acids, organic acids, fatty acid, phenolic and other compounds, and discuss them separately.Eleven amino acids, including Alanine , beta alanine , Glycine , Isoline , Leucine , Lysine , Phenylalanine , Proline , Serine , Threonine , and Valine , were significantly up-regulated in response to nano-Cu in a dose-dependent way . The increased exudation of amino acids is likely an active defense response of the cucumber plant. The up-regulated amino acids can provide many binding sites for copper, hindering the translocation from the root cell membrane. Previous studies showed that amino acids play an important role in chelating Cu2+. It is reported that amino acid complexes formed with other metals, e.g. Ni, are much more stable than those with carboxylic acids.Cu in the roots of Cu-tolerant A. maritima exists as a Cu−proline complex.EXAFS spectra demonstrated Cu complexation with the nonproteogenic amino acid nicotianamine, which shows very high affinity for Cu.Kupper et al. assumed that plants keep dissolved metals out of the cytoplasm and sequester/ complex them into the vacuole or cell wall.The upregulated amino acids may also reflect an attempt by the cucumber plants to sequester Cu in stems. Although stem metabolites were not analyzed, it is possible that amino acids are also secreted in the xylem sap to bind with Cu2+ in the transpiration stream. It is reported that more than 99% Cu in tomato and chicory xylem sap was in a bound form with histidine and nicotianamine .Amino acids in root exudate not only bind metals, but also serve as signaling molecules and have an antioxidant defense function.If the upregulation of these amino acids is an active defense of cucumber plant to excess nano-Cu/Cu ions, the increased amino acids possibly will decrease the uptake of Cu by cucumber plants. In order to verify this hypothesis, two-weekold cucumber plants were cultivated in 20 mg/L nano-Cu nutrient solution with different levels of Ser for 48 h. Interestingly, Cu accumulation in roots decreased with increasing Ser concentration,growing strawberries vertical system even though the free Cu ions in nutrient solution were much higher in the presence of Ser.

After the plants were removed, the pH in nutrient solutions was determined. As shown in Figure 5, the pH decreased from 6.37 to 6.01 as the Ser concentration increased from 0 to 25 mM, which may explain why more Cu ions were released in the presence of Ser compared to the control . Those results strongly indicate that amino acids are possibly released to detoxify nano-Cu by binding with Cu ions. However, we cannot rule out the possibility that up-regulation of some amino acids was due to membrane damage, which caused the leakage.Organic acids are strong cation chelators, which play an important role in facilitating mineral element uptake and sequester or exclude toxic metals. Several studies have shown that citric, oxalic, and succinic acids are involved in the detoxification of various dissolved metals.GC-MS results showed citric, succinic, malic, and fumaric acids were the most abundant low molecular weight organic acids in cucumber root exudates, which is consistent with previous reports on organic acid composition in cucumber root exudates. Surprisingly, patterns of succinic, malic, and fumaric acids were not changed by nano-Cu , which indicates those organic acids did not respond to Cu stress. In contrast, citric acid, the most abundant organic acid, was down-regulated by nano-Cu . Citric acid in root exudate decreased 5× at 10 ppm nano-Cu and 60× at 20 ppm in treated cucumber plants compared to the control. It is known that organic acids play an important role in restricting the passage of metals across the root, due to their strong affinity to form stable extracellular complexes with Cu, Al, and Cd.Other reports showed organic acids in the rhizosphere help solubilize minerals and facilitate their uptake by the plant.Citric acid has been shown to assist copper uptake in a moderate-accumulator plant .The down-regulation of citric acid is possibly an active process to decrease the dissolution, uptake, and translocation of Cu into cucumber tissues, or it could represent a shift in metabolism in the tricarboxylic acid cycle . As mentioned before, citric acid can play a dual role: it can either mobilize metals to accelerate uptake in plants that are deficient in some elements,or it can complex with metals to hinder their translocation.In this study, we hypothesized that citric acid played a role in mobilizing Cu ions release from nano-Cu, increasing Cu accumulation in cucumber plants. To confirm this hypothesis, we conducted an additional experiment in which we exposed cucumber plants to 20 mg/L nano-Cu at different concentrations of citric acid . We found that the pH of the hydroponic system decreased from 6.37 to 5.28 . This decrease in pH led to increased dissolved Cu ions to concentrations that were 8 times higher than that in the control .

This result indicates that citric acid has a strong ability to dissolve nano-Cu by decreasing the system pH. Therefore, it is not surprising that Cu levels in cucumber plants grown in 20 mg/L nano-Cu in the presence of 6.25 mM citric acid were 4 times higher than that in plants grown in 20 ppm nano-Cu without additional citric acid . However, it is noteworthy that citric acid at this concentration may damage biological membranes and lead to passive uptake of Cu through leaky membranes. At least, these additional experiments demonstrate that citric acid increased nano-Cu dissolution in cucumber plants. Taken together, the up-regulation of amino acids and down-regulation of citric acid are likely plant strategies to hinder the uptake of Cu and detoxify the Cu toxicity.The release of fatty acids from the membrane is involved in plant tolerance to biotic and abiotic stresses.Pelargonic acid was up-regulated in root exudates after exposure to nano-Cu . Pelargonic acid is a natural non-selective herbicide, which can disrupt intercellular pH and membrane integrity causing rapid cell death Evidence has shown that pelargonic acid participates in stress response and can be an indicator of root membrane damage.The increased pelargonic acids in nano-Cu treated root exudates may be an indicator of membrane damage. Copper also interferes with fatty acid metabolism.Phenolics are secondary metabolites with an important role in stress response.The concentrations of salicylic and benzoic acids were up-regulated in the presence of nano-Cu/Cu, especially salicylic acid . Both compounds are reported to have antioxidant and anti-fungal activities and play a crucial role in plant defense against a variety of biotic and abiotic stressors.The concentrations of salicylic acid in root exudate of 10 and 20 ppm nano-Cu treated plants were 13 and 26 times higher than that in the control. It is reported that salicylic acid serves as an internal signaling molecule in the activation of plant defense after pathogen attack.Previous studies also suggested salicylic acid treatment significantly reduced malondialdehyde and H2O2 concentrations in the roots and leaves of rice under Cu stress, therefore alleviating Cu toxicity.In addition, 4-hydroxybenzoate, a phenolic derivative of benzoic acid, which is a secondary metabolite and also plays a key role in stress response, was up-regulated by exposure to nano-Cu. The up-regulation of these three phenolics is possibly a self-protection mechanism of cucumber to nano-Cu exposure at these levels.

As shown in Figure 3, most of the down-regulated compounds are sugar-related metabolites, which might explain why citric acid exudation decreased as it was preserved for the TCA cycle. It is interesting to find that the level of dehydroascorbic acid in nanoCu treated root exudates is apparently down-regulated . DHA is known to participate in the plant defense against oxidative stress,growing vegetables in vertical pvc pipe and it is also an oxidized form of ascorbic acid. Dehydroascorbate is an intermediate product of the reaction between ascorbic acid and ROS, and can be oxidized to threonic acid. Thus, the down-regulation of DHA is an indicator that ROS was triggered by nano-Cu in the rhizosphere and a response to oxidative stress occurred. It is possible that the membrane damage occurred due to lipid peroxidation induced by ROS.Because the nutritional sources of microbes in the rhizosphere come from root exudates,the altered pattern of amino acids, carboxylic acids, phenolics, and sugar metabolites may possibly affect microbial activities and communities in the rhizosphere. Yuan et al. revealed that n-CeO2 did not affect soil bacterial communities in the absence of soybean plants, but did affect them in the presence of soybean plants, likely through the change of quantity and composition of root exudates. Our results indicate that nano-Cu altered the metabolite profile in cucumber root exudates, and this change may alter the mutually beneficial feedback interactions between plant and microbes in the rhizosphere. Root exudate as a hidden part of plant defense system, has been neglected or underestimated in previous studies investigating plant-related nanotoxicity. In this study, the profiling analysis of root exudate metabolites revealed important detoxification mechanisms of cucumber plants to nano-Cu induced stress. In addition, 1 H NMR and GC-MS based metabolomics provided a comprehensive understanding of the changes in metabolites induced by exposure to nano-Cu, and this powerful combination of analytical techniques may be very useful in revealing effects of other NPs on different plant tissues, even at sublethal NP concentrations. The findings reflect the situation in hydroponic media, which is quite relevant for cucumber production in many parts of the world. However, the results may be different in soil media. Further studies are clearly needed to elucidate the contribution of membrane damage to up-regulated metabolites in root exudate.The Fusarium wilt fungus and the root knot nematode Chitwood; RKN are important soil-borne pathogens causing severe damage in watermelon production throughout the world.

Symptoms of Fusarium wilt at the seedling stage include seedling dieback and a scorched appearance. In mature plants, tissue chlorosis and unilateral wilting can be observed after loss of turgor pressure. As the disease progresses, complete vine wilting is often observed. FON has four physiological races based on variability in aggressiveness on differential cultivars. RKN is an obligatory parasite that induces galls on the infected root system of a susceptible host. Galls disrupt the vascular system of plants making them grow poorly and can lead to plant death under heavy infestation. Pre-plant fumigant application with methyl bromide was often used and had been effective in reducing both FON and RKN in the watermelon production system. Phasing out of MeBr in accordance with the Montreal Protocol resulted in limited options for managing both soil-borne pathogens.Triploid seedless watermelon cultivars, that are currently cultivated widely, do not possess a high level of resistance against FON race 2. To further complicate the issue, FON race 3 has also been identified in several states of the U.S.. Proline is the only effective fungicide labeled for use on watermelon to manage FON. Increased selection pressure on FON pathogen populations might lead to increased resistance to the fungicide. Grafting susceptible watermelon scions to inter specific hybrid squash and bottle gourd Standl can be a viable option for FON management. Two drawbacks with bottle gourd and C. moschata × C. maxima hybrid rootstocks are their susceptibility to root-knot nematode and the higher expense of grafted plants. Therefore, available disease control options should be combined with alternative strategies for the integrated management of FON. Plant disease resistance is affected by the plants’ genetics and by the environment in which it is grown, including nutrient deficiencies and toxicity. Induced resistance has been proposed as one of the explanations for the interaction between specific nutrients and degree of resistance to plant pathogens. Induced resistance is a plant-based defense system that is elicited by specific environmental stimuli, which enables them to resist biotic challenges. These defense responses include the oxidative burst, changes in cell composition and synthesis of antimicrobial compounds such as phytoalexins. The involvement of mineral nutrients in inducing resistance has been studied in several plant-pathogen systems. For instance, several reports indicate that potassium salts can be used for the induction of host-resistance against powdery mildew on cucumber, pepper, tomato and sugar beet. Potassium application has also been shown to increase downy mildew in muskmelon , caused by Pseudoperonospora cubensis, and Microdochium patch caused by Microdochium nivale in creeping bentgrass. Despite these reports, the impact of a particular nutrient cannot be generalized for all plant-pest/pathogen systems, either globally or individually.