Antifungal Activity of Copper Oxide Nanoparticles against Root Rot Disease in Cucumber

Metal oxide nanoparticles have recently garnered interest as potentially valuable substances for the management of plant diseases. Copper oxide nanoparticles (Cu2ONPs) were chemically fabricated to control root rot disease in cucumbers. A scanning electron microscope (SEM), X-ray diffraction (XRD) and photoluminescence (PL) were employed to characterize the produced nanoparticles. Moreover, the direct antifungal activity of Cu2ONPs against Fusarium solani under laboratory, greenhouse, and field conditions were also evaluated. In addition, the induction of host-plant resistance by Cu2ONPs was confirmed by the results of enzyme activities (catalase, peroxidase, and polyphenoloxidase) and gene expression (PR-1 and LOX-1). Finally, the effect of Cu2ONPs on the growth and productivity characteristics of the treated cucumber plants was investigated. The average particle size from all the peaks was found to be around 25.54 and 25.83 nm for 0.30 and 0.35 Cu2O, respectively. Under laboratory conditions, the study found that Cu2ONPs had a greater inhibitory effect on the growth of Fusarium solani than the untreated control. Cu2ONP treatment considerably reduced the disease incidence of the root rot pathogen in cucumber plants in both greenhouse and field environments. Defense enzyme activity and defense genes (PR1 and LOX1) transcription levels were higher in cucumber plants treated with Cu2ONPs and fungicide than in the untreated control. SEM analysis revealed irregularities, changes, twisting, and plasmolysis in the mycelia, as well as spore shrinking and collapsing in F. solani treated with Cu2ONPs, compared to the untreated control. The anatomical analysis revealed that cucumber plants treated with Cu2ONPs had thicker cell walls, root cortex, and mesophyll tissue (MT) than untreated plants. Cucumber growth and yield characteristics were greatly improved after treatment with Cu2ONPs and fungicide. To the best of our knowledge, employing Cu2ONPs to treat cucumber rot root disease is a novel strategy that has not yet been reported.


Introduction
In Egypt, cucumbers (Cucumis sativus L.) are among the most important cucurbitaceous crops and the leading export vegetable. Cucumbers are grown under protected cultivation conditions in plastic greenhouses in two main growing seasons, i.e., autumn and winter. strategies for controlling plant pathogens in different crops is the use of systemic acquired resistance (SAR) on a large scale [34].
Thus, the current study aims to carry out the following objectives: (1) to fabricate Cu 2 ONPs of unique size and shape, verify their direct antifungal activity against F. solani in vitro, (2) to evaluate their ability to induce systemic resistance against root rot disease in cucumber plants in greenhouse and field conditions, (3) to determine the mechanism of resistance induction through the expression of regulatory and defense genes and the activity of defense enzymes and finally, (4) to look into the impact of produced nanoparticles on some of the growth and production features of cucumbers that have been treated.

Fabrication of Cu 2 ONPs
Cu 2 ONPs were chemically prepared using a low-cost precipitation method, where 1 M copper sulfate (CuSO 4 . 5H 2 O) was dissolved in 100 mL deionized water (DI), followed by the addition of 5 M sodium hydroxide (NaOH), which was also dissolved in 100 mL DI. The reaction occurs at room temperature, after which different quantities of glucose solution (C 6 H 12 O 6 H 2 O) (0.30, 0.35 M) were heated to 50 • C and dropped into the mixture to reduce CuO to Cu 2 O nanoparticles. The precipitates were collected and centrifuged, then washed five times with DI and ethanol, respectively, before being dried for 24 h at 100 • C.

Characterization of Cu 2 ONPs
SEM (JSM-651OLV) and X-ray diffraction (XRD, Shimadzu 6000) were used to investigate the crystal structure and morphological properties of the Cu 2 ONPs, respectively. The samples' optical properties were investigated using a Kimmon He-Cd (325 nm) photoluminescence excitation laser, and the spectra were obtained using a HORIBA iHR320 spectrometer with a Synapse CCD camera. From XRD patterns, the particle size can be calculated employing Scherrer's formula [35], which is as follows: where K is a shape factor and is usually taken to be 0.94, λ is the wavelength of the incident X-ray (Cu Kα1, 0.15406 nm), θ is the angle of Bragg, and β is the total width at half maxima (FWHM) in radians.

Plant Materials
Cucumber (Cucumis sativus L.) seeds of cv. Beta alpha were obtained from the Horticulture Research Institute, Agricultural Research Center (ARC), Dokki, Giza, Egypt.

Fungal Pathogen Identification
F. solani was isolated from naturally infected cucumber plants that displayed dampingoff and root rot symptoms. Cucumber samples were collected from various cultivated areas in Egypt's Giza Governorate. The isolated fungus was purified with the hyphal tip technique and identified using morphological and microscopic features [36]. The identification of fungal isolates was confirmed morphologically at the Plant Pathology Research Institute (PPRI), Agricultural Research Center (ARC), Giza, Egypt. The identified fungus was kept in a potato dextrose agar (PDA) medium at 4 ± 1 • C [37].

Pathogenicity Test
An inoculum of the pathogen F. solani was prepared by growing the isolate in autoclaved bottles containing (100 g sorghum, 50 g sand, and 80 mL water) and incubated at 25 ± 2 • C. The sandy loam soil was autoclaved at 121 • C for 2 h. Plastic pots (30 cm in diameter) were sterilized using 5% formalin and left for 2 days to ensure complete formalin evaporation. Soil infestation was carried out by adding the previous inoculum to each pot at the rate of 3% of the soil weight. Five surface-sterilized cucumber seeds were sown in each pot seven days after soil infestation under controlled greenhouse conditions (25 ± 2 • C, 65 ± 2% humidity). Five replicates were used for each treatment, and pots with pathogen-free sandy loam soil were used for planting a control treatment. The percentage of damping-off at 15, 30, and 45 days after sowing was recorded.

Effects of Cu 2 ONP Concentrations on Fungal Growth
The fungal isolate was cultured on a PDA medium for 7 days, then plugs (5 mm) were re-cultured again onto new PDA plates (9 mm), treated with two concentrations (50 and 100 µg/L) of 0.30 and 0.35 M Cu 2 O NPs, respectively. The fungicide Uniform 390 SE (azoxystrobin + mefenoxam), produced by Syngenta company, Basel, Switzerland, was used as a recommended fungicide against soil-borne disease at an application rate of 1.5 L/hectare). Five plates served as duplicates for each treatment. Plugs (5 mm) of F. solani grown on PDA were used as a control.

In Vivo (Greenhouse) Experiment
Cucumber seeds were planted at a rate of 5 seeds per pot. Five pots were used for each treatment. Infested soil with the pathogenic agent inocula was prepared as mentioned above in the section of the pathogenicity test. All pots were irrigated three times throughout the seven days. In this experiment, 0.30 and 0.35 M Cu 2 ONPs were applied at a concentration level of 100 µg/L, and the fungicide was used at 1.5 L/hectare. All treatments were applied by immersing the seeds for 60 min in the solution before sowing. The experimental design was a randomized complete block. The greenhouse conditions were 24 • C and 60% humidity. The percentages of pre-and post-emergence damping-off and survived plants were calculated according to Shaban and El-Bramawy [38], while root rot assessment was recorded according to the scale 0-4 of Hwang and Chang [39], with minor modifications, which were as follows: 0 = healthy roots, 1 = 1-9%, 2 ≥ 9-39%, 3 ≥ 39-69% and 4 ≥ 69% and above for root discoloration. Root discoloration was recorded at the end of the experiment and calculated according to the following formula: Disease incidence (DI%) = number of infected plants/total plants in the treatment × 100 Root rot index = (total of all ratings/(total number of plants × 4)) × 100 2.8. Laboratory Studies 2.8.1. Enzyme Activity Assay To evaluate the effect of the tested treatments on the activity of defense enzymes (catalase, peroxidase, and polyphenol oxidase) in the treated cucumber plants, 0.5 g of freshly treated cucumber leaves were homogenized at 0-4 • C in 3 mL of 50 mM TRIS buffer (pH 7.8), containing 1 mM EDTA-Na 2 and 7.5% polyvinylpyrrolidone. The homogenates were centrifuged (12,000 rpm, 20 min, 4 • C), and the enzyme activity was estimated at 25 • C, using a typical UV-160A spectrophotometer. Catalase (CAT), peroxidase (POX), and polyphenol oxidase (PPO) activities were measured, as demonstrated by Aebi [40], Hammerschmidt et al. [41], and Malik and Singh [42], respectively.

RT-PCR Analysis
One week after germination, a 100 mg sample of cucumber leaf tissue was taken from the treated and control plants. With a pre-chilled mortar and pestle, the samples were immediately crushed in liquid nitrogen. Total RNA was extracted as explained by Tek and Calis [43]. The isolated RNA was utilized for qRT-PCR amplification. All qRT-PCRs were performed with real-time PCR equipment using the SYBR green method. The specificity was tested by creating a melting curve by progressively increasing the temperature to 95 • C. The gene-specific primers (PR-1 and LOX-1) were used in quantitative RT-PCR (Table 1). To normalize the transcript levels for each sample, the actin gene was used as a reference gene, and the final data were calculated using the formula 2 −∆∆CT [44]. Table 1. Forward and reverse primers sequence for PR-1, LOX-1 and actin genes.

Microscopic Observations of Fungal Morphology
A light microscope (Leica DM1000) examination was used to study the effect of Cu 2 ONPs on mycelia and spores of F. solani. To study the interaction between F. solani, the cause of damping-off and root rot of cucumber plants and copper oxide nanoparticles Cu 2 ONPs (0.35) and Cu 2 ONPs (0.30), small pieces of agar were cut at the parts embedded with copper oxide nanoparticles with F. solani growth and transferred for dehydrating and were subsequently sputter-coated with gold according to methods of Harley and Ferguson [45]. Examination and photographing were carried out using a scanning electron microscope (SEM), JEOL JSM 6510 Iv, at the Faculty of Agriculture, Mansoura University, to observe the copper oxide nanoparticles' effects through parasitism action.

The Anatomical Structure of Cucumber Plants
The anatomical structure of the median internode of the main roots and the grafting zone of 40-day old cucumber plants infected with F. solani and treated with 0.30 and 0.35 M Cu 2 ONPs were investigated. The samples were sliced and fixed in a solution made up of 10 mL formalin, 5 mL glacial acetic acid, and 85 mL 70% ethyl alcohol. Following that, the samples were washed in 50% ethyl alcohol, dried in a standard butyl alcohol series, embedded in paraffin wax at 56 • C (melting point), and cut with a rotary microtome. Finally, crystal violet and erythrosine prepared in Canada balsam were used to stain the samples [46]. An optical microscope was used to examine the slides, and counts and measures (m) for various tissues were calculated.

Field Experiment
A field experiment was conducted to evaluate the efficiency of Cu 2 ONPs and the recommended fungicide against the damping-off disease of cucumber. The experiment was designed in a randomized complete block with four replicates. The field in which the experiment was conducted has a previous history of the disease. Whether it was 0.30 or 0.35 M, Cu 2 ONPs were used at a rate of 100 µg/L and the fungicide at 1.5 L/ha. Each replicate was 2 × 10 m 2 in the area and had two rows of 1 m in width and 10 m in length. Then, the soil was irrigated for 7 days before sowing. Cucumber seeds (cv. Beta Alpha) were planted at a spacing of 50 cm at a rate of 3 seeds per hole (after soaking in the tested treatments for 1 h). The effectiveness of the treatments in lowering damping-off and disease incidence in pre-and post-emergent stages, as well as the percentages of healthy plants that survived, were recorded after 15, 30, and 45 days. The percentages of pre-and postemergence damping-off and survived plants were estimated according to the previously described method.

Growth and Yield Parameters
Plant height, root length, wet weight and dry weight were evaluated in both treated and untreated cucumber plants to evaluate the influence of the tested treatments on some growth characteristics of cucumber plants. According to Torres-Netto et al. [47], the total chlorophyll content in fully expanded cucumber leaves was determined using a portable paper chlorophyll meter (Minolta SPAD-502, Osaka, Japan). Shoot length was measured from the base of the cucumber plants to the top in centimeters; root length was measured from the base of cucumber plants to the top root in centimeters. Fresh weight was measured in grams and the dry weight of plants (80 • C for 36 h) was measured in grams when the weight was stable. Yield parameters, such as the number of fruits/plant, fruit weight (g), fruit weight/plant (kg), and % rate of increase yield, were measured.

Statistical Analysis
All experiments were designed with a complete randomized block design. The WASP software (Web Agriculture Stat Package) was used for the analysis of variance (ANOVA) at p ≤ 0.05. Using the SPSS v.22 software, analysis of variance and Pearson correlation tests were run to determine the relationship between all the measured parameters in this study.

Characterization of Cu 2 ONPs
The crystal structure of the fabricated nanoparticles was examined by XRD, as presented in Figure 1A [45,46]. All the observed diffraction peaks are associated with the standard polycrystalline cubic structure of Cu 2 O with the Pn3m group space (JPCD NO. 05-0667) [48,49]. Only a pure Cu 2 ONP phase is formed when no peaks for other phases appear. Moreover, the intensity (111) peak shows the high quality of crystallization. The calculated values for the particle size from the highest diffraction peak (111) were found to be around 30.96 and 31.91 nm for 0.30 and 0.35 Cu 2 ONPs, respectively. In addition, the average particle size from all the peaks was found to be around 25. 54  the responsible for the broad peak that can produce oxygen vacancies and/or copper interstitials [35]. This peak may be also due to the phonon-assisted excitations from the recombination process in nanoparticles [35]. The other peak resulted from the existence of other defects formed during the growth process, such as oxygen vacancies [35].   Figure 1C,D display the top-view SEM images of the fabricated Cu 2 ONPs. It is noticeable that Cu 2 ONPs demonstrate the morphology of cubic structures [35]. The results confirm and agree with the XRD measurements. From SEM images, the distributions of grain size for the fabricated samples are calculated, as shown in Figure 2A. It is clear that the grain size for the 0.30 Cu 2 ONPs is smaller than the 0.35 Cu 2 ONPs, where its average values were around 0.7 and 0.9 µm, respectively. Therefore, the surface area of 0.30 is higher than 0.35. Such a change in the particle size, average grain size, and surface area for the Cu 2 O NPs is attributed mainly to the glucose amount during the reduction of CuO to Cu 2 ONPs, where glucose acts as a reduced agent and surfactant agent at the same time. In such a case, the increase in glucose prevents the agglomeration of the Cu 2 ONPs and increases the lateral and vertical growth, which produces smaller particle sizes and grain sizes for 0.30 Cu 2 ONPs than 0.35 Cu 2 ONPs [50,51].

Antifungal Activity of Cu2ONPs Against F. solani under Laboratory Conditions
The effects of Cu2ONPs with its two molar concentrations, Cu2ONPs (0.35) and Cu2ONPs (0.30), on the mycelial growth of F. solani compared to the fungicide are presented in Table 2 and Figure 3. The results showed that the used Cu2ONPs and the fungicide significantly inhibited the growth of F. solani compared to the untreated control. The most effective treatment was the fungicide, followed by Cu2ONPs (0.30 M) and Cu2ONPs (0.35 M), respectively. In addition, there was a strong correlation between the inhibition percentage of the tested treatments and their concentrations. Photoluminescence (PL) is a technique used to examine the recombination rate of produced electron-hole pairs and the quality of crystal for the fabricated materials [52,53]. Thus, PL spectra of the synthesized Cu 2 ONPs were described, as shown in Figure 2B,C. The PL spectrum has two emission peaks, which cover up the visible light region. The first one is broader and varies from around 360 to 610 nm and is centered at about 520 nm. The other has smaller intensity and less broadening and is centered at about 705 nm. Excitonic transition series of Wannier hydrogen-like electrons associated with deep-level defects are the responsible for the broad peak that can produce oxygen vacancies and/or copper interstitials [35]. This peak may be also due to the phonon-assisted excitations from the recombination process in nanoparticles [35]. The other peak resulted from the existence of other defects formed during the growth process, such as oxygen vacancies [35].

Antifungal Activity of Cu 2 ONPs against F. solani under Laboratory Conditions
The effects of Cu 2 ONPs with its two molar concentrations, Cu 2 ONPs (0.35) and Cu 2 ONPs (0.30), on the mycelial growth of F. solani compared to the fungicide are presented in Table 2 and Figure 3. The results showed that the used Cu 2 ONPs and the fungicide significantly inhibited the growth of F. solani compared to the untreated control. The most effective treatment was the fungicide, followed by Cu 2 ONPs (0.30 M) and Cu 2 ONPs (0.35 M), respectively. In addition, there was a strong correlation between the inhibition percentage of the tested treatments and their concentrations.

Effect of Cu2ONPs on Disease Incidence under Greenhouse Conditions
The effect of Cu2ONPs compared to the recommended fungicide on the damping-off percentage and root rot disease incidence in the treated cucumber plants under greenhouse conditions is presented in Table 3. The results showed that 0.30 and 0.35 M of Cu2ONPs and the chemical fungicide significantly reduced the damping-off percentage and disease incidence in treated cucumber plants compared to the untreated control. The highest reduction in damping-off percentage and disease incidence was recorded for the recommended fungicide, followed by 0.30 and 0.35 M of Cu2ONPs, respectively. The

Effect of Cu 2 ONPs on Disease Incidence under Greenhouse Conditions
The effect of Cu 2 ONPs compared to the recommended fungicide on the damping-off percentage and root rot disease incidence in the treated cucumber plants under greenhouse conditions is presented in Table 3. The results showed that 0.30 and 0.35 M of Cu 2 ONPs and the chemical fungicide significantly reduced the damping-off percentage and disease incidence in treated cucumber plants compared to the untreated control. The highest reduction in damping-off percentage and disease incidence was recorded for the recommended fungicide, followed by 0.30 and 0.35 M of Cu 2 ONPs, respectively. The reduction in the damping-off percentage and disease incidence in cucumber plants treated with 0.30 M of Cu 2 ONPs was significantly higher than that of 0.35 M of Cu 2 ONPs.

Effect of Cu 2 ONPs on the Activity of Defense Enzymes in Treated Cucumber Plants
The effect of Cu 2 ONPs and the recommended fungicide on the activity of defense enzymes in the treated cucumber plants is presented in Table 4. The data presented in Table 4 indicated that Cu 2 ONPs and the recommended fungicide significantly increased the activities of defense-related enzymes, i.e., catalase, peroxidase and polyphenol oxidase in treated cucumber plants compared to the untreated control. The highest activity for defense enzymes was recorded for 0.30 M Cu 2 ONPs, followed by 0.35 M Cu 2 ONPs and fungicide, respectively.

Relative Expression Assay
Defense gene transcriptions were substantially up-regulated among Cu 2 ONP treatments ( Figure 4). Increased relative transcription levels of the PR-1, and LOX-1 genes analyzed by qRT-PCR were observed in the treated cucumber plants at 7 days after treatment. It was revealed that in the Cu 2 ONP-treated plants, there were more up-regulated PR-1 and LOX-1 than in the control group, and that the Cu 2 ONP (0.30M)-treated plants had slightly higher PR-1 and LOX-1 transcription levels than the Cu 2 ONP (0.35 M) group. The relationship between the cucumber and F. solani was found to be mediated by some genes. The relationship between the cucumber and F. solani was found to be mediated by some genes.

Microscopic Observations of Fungal Morphology
Light microscope examinations of F. solani mycelia and spores treated with 0.30 and 0.35 M Cu 2 ONPs revealed shrinking, twisting, and collapse of treated plants ( Figure 5B,C), compared to untreated F. solani (control) ( Figure 4A).
Scanning electron microscope examination of the fungal structures taken from cucumber roots treated with 0.30 and 0.35 M Cu 2 ONPs showed abnormalities and alterations in the mycelia of F. solani ( Figure 6B), compared to the untreated control ( Figure 6A). Moreover, twisting and plasmolysis of mycelial and spores and shrinking and collapsing were also observed in the roots of the treated cucumber plants ( Figure 6B).    Figure 6B), compared to the untreated control ( Figure 6A). Moreover, twisting and plasmolysis of mycelial and spores and shrinking and collapsing were also observed in the roots of the treated cucumber plants ( Figure 6B).

Effect of Cu2ONPs on Disease Incidence in Two Locations under Field Conditions
The effect of Cu2ONPs compared to the recommended fungicide on damping-off percentage and root rot disease incidence in cucumber plants in Menoufia and Giza Governorates is presented in Table 5. The results showed that 0.30 and 0.35 M of Cu2ONPs and the chemical fungicide significantly reduced the damping-off percentage and disease incidence in the treated cucumber plants compared to the untreated control in the two locations. The highest reduction in damping-off percentage and disease incidence was recorded for the recommended fungicide, followed by 0.30 and 0.35 M of Cu2ONPs in the two locations. The efficacy of Cu2ONPs and the recommended fungicide was higher in Giza than in Menoufia Governorate.

Effect of Cu 2 ONPs on Disease Incidence in Two Locations under Field Conditions
The effect of Cu 2 ONPs compared to the recommended fungicide on damping-off percentage and root rot disease incidence in cucumber plants in Menoufia and Giza Governorates is presented in Table 5. The results showed that 0.30 and 0.35 M of Cu 2 ONPs and the chemical fungicide significantly reduced the damping-off percentage and disease incidence in the treated cucumber plants compared to the untreated control in the two locations. The highest reduction in damping-off percentage and disease incidence was recorded for the recommended fungicide, followed by 0.30 and 0.35 M of Cu 2 ONPs in the two locations. The efficacy of Cu 2 ONPs and the recommended fungicide was higher in Giza than in Menoufia Governorate.

Effect of Cu 2 ONPs on Total Chlorophyll and Growth Parameter of Cucumber Plants under Field Conditions
The results in Table 6 indicated that the applied Cu 2 ONPs (0.30 and 0.35 M) and fungicide increased the growth parameters of treated cucumbers, such as total chlorophyll (SPAD), shoot length (cm), root length (cm), fresh and dry weight (g), under field conditions in the two locations compared to the untreated control. The highest growth parameters in the treated cucumbers were for the chemical fungicide, followed by 0.30 and 0.35 M of Cu 2 ONPs, respectively. Approximately, there are no significant differences in the measured growth parameters of cucumbers between Cu 2 ONPs 0.30 and 0.35 M in the two locations. The measured growth parameters of cucumber treated with Cu 2 ONPs and the fungicide were significantly higher in Giza Governorate than in the Menoufia Governorate. Statistical comparisons were made among treatments within a single column. * The different letters represent significant differences using Fisher's LSD test at p ≤ 0.05. * Each mean value came from three replicates.

Effect of Cu 2 ONPs on Yield Parameter of Cucumber Plants under Field Conditions
The results in Table 7 indicated that the applied Cu 2 ONPs (0.30 and 0.35 M) and fungicide increased the yield parameters of treated cucumbers, such as the number of fruits, fruits weight/plant, weight of fruits and rate of increased yield, under field conditions in the two locations compared to untreated control. The highest yield parameters in the treated cucumbers were for the chemical fungicide, followed by 0.30 and 0.35 M of Cu 2 ONPs, respectively. With regard to the measured yield parameters in the two locations, there are approximately no significant differences between Cu 2 ONPs (0.30) and the fungicide used. The measured yield parameters of the treated cucumbers were significantly higher in the cucumber plants treated with 0.30 M than with 0.35 M Cu 2 ONPs in the two locations.

Pearson Correlation
The relationship between the efficacy of the tested treatments and total chlorophyll, stem length (cm), root length (cm), fresh weight (g), dry weight (g), number of fruits, weight of fruits/plant, and rate of yield increase is indicated as shown in Table 8. The correlations between these variables were strongly positive and ranged between 0.904 and 0.998, which indicates the ability of these treatments under study to control this disease and increase growth and yield parameters.

Discussion
The pathogenic cucumber fungus F. solani is a common fungal genus that causes seed rot in cucumber seedlings, as well as pre-and post-emergency suppression of cucumber seedling production [54]. Cu 2 ONPs were examined in this work to control F. solani in cucumbers under laboratory, greenhouse and field conditions, and the results revealed a considerable reduction in the disease's occurrence. In this investigation, copper oxide nanostructures were found to have promising antifungal action against F. solani under laboratory conditions. This is in agreement with [29], who found that copper oxide nanoparticles inhibited F. solani cultures significantly. Furthermore, the results agreed with those of Elmer and White [31], Elmer et al. [33], and Khatami et al. [29], who found that Cu 2 ONPs had a high potential for controlling soil borne fungi, such as F. solani and F. oxysporum. Consolo et al. [55] showed that both Ag and Cu 2 ONPs caused a significant reduction in the mycelia development of A. alternata and P. oryzae in a dose-dependent concentration. Moreover, copper compounds are still employed as fungicides to protect wood and prevent plant diseases [56,57]. From another point of view, copper oxide is a non-toxic, inorganic antimicrobial agent that inhibits the growth of a wide range of microbes [58][59][60][61][62]. The precise mechanism of copper oxide nanoparticles' antimicrobial activity is still unknown. Researchers have proven in some published studies that the antibacterial activity may be related to the inactivation of the DNA enzyme, and as a result, impedes replication and growth inhibition [29]. Generally, some researchers discovered that NPs operate directly as antibacterial agents, while others discovered that their main role is to change the host's nutritional status and activate defense mechanisms. Copper can be directly poisonous to microorganisms. Moreover, as fertilizer, Cu appears to contribute to host defense [33].
Accordingly, the obtained results show a significant reduction in the damping-off percentage and disease incidence in the cucumber plants treated with 0.30 and 0.35 M of Cu 2 ONPs under greenhouse and field conditions (Menoufia and Giza Governorates) compared to the untreated plants. As explained by some researchers, Cu 2 ONPs have high efficacy against several pathogens that cause damping-off and root rot, making them a viable alternative to fungicides in cucumber protection. It has a dual effect. The first is that it is directly toxic to diseases, and the second is that it can be used as a fertilizer, while also increasing the plant's natural defenses against pathogens. Due to their long-standing usage as contact bactericides and fungicides, CuNPs are also an essential choice in plant disease management [27,31,63].
The induction of host-plant resistance by Cu 2 ONPs was confirmed by the results of enzyme activities (catalase, peroxidase, and polyphenoloxidase) and gene expression (PR-1 and LOX-1). This was shown by the fact that Cu 2 ONPs caused an increment in the activity of catalase, peroxidase, and polyphenol oxidase, as well as in the gene expression of PR-1, and LOX-1. Elmer [33] provided an explanation for this by demonstrating how the presence of both Cu 2 ONPs and F. oxysporum f. sp. niveum strongly up-regulated the gene expression for polyphenol oxidase (PPO) and PR1 in watermelon roots. The PPO enzyme assay results supported the gene expression findings. In order to effectively provide this micronutrient to fight disease, Cu 2 ONPs may be used. According to Ashraf et al. [64], treatment with varying concentrations of CuO-CFNPs resulted in an upward trend in photosynthetic pigments, phenolic content, and stress/antioxidant enzymatic components. In addition, PR-1 is a gene that is often expressed if SAR activity is stimulated [65]. Similarly, transcriptions were increased in Cu 2 ONP treatments. The biosynthesis process of jasmonic acid, the phytohormone that controls ISR, begins with the synthesis of LOX-1, which is the first enzyme produced in this pathway [65].
The effect of Cu 2 ONPs in controlling the disease was also confirmed using a light microscope, a scanning electron microscope, and anatomical characteristics. The significant effect of Cu 2 ONPs was observed on mycelia and spores (abnormalities and alterations, twisting, plasmolysis, shrinking and collapsing) of F. solani. In addition, the cell wall, root cortex, and mesophyll tissue (MT) thickness were all increased with the treatment by Cu 2 ONPs, in comparison to the untreated plants, where the cell wall was ruptured. According to Ashraf et al. [64], comparative exposure to larger concentrations has severe negative consequences on the mycelial surface, resulting in split, distorted, and collapsed structures with tiny vesicles, similar to polyps. It was proposed that Cu-NPs released Cu ions into the growth media, which could diffuse past the cell wall and bond with the surface of fungal cells. Our findings unmistakably demonstrate that fungal mycelia become distorted following treatment with Cu 2 ONPs, which may be related to the interruption of chitin synthesis. Another interpretation revealed that the properties and chemical content of the nanoparticles, as well as their size and surface coating, when they interact with plants, cause several morphological and physiological changes [66].
These findings were in line with those of Elsharkawy et al. [67], who demonstrated that chitosan nanoparticles improved the thickness of the mesophyll tissue (MT), the thickness of the lower and upper epidermis (LE and UE), and the bundle length and width in the midrib in comparison to the control of treated wheat plants. Furthermore, Kim et al. [68] discovered that due to the disruption of the membrane integrity, Candida albicans' normal budding process was inhibited and the structure of the cell membrane was disrupted.
From another point of view, cucumber plants treated with Cu 2 ONPs and a fungicide grew better and demonstrated a better yield in the Governorates of Menoufia and Giza, according to this study. Elmer and White [31] found that foliar spraying of CuONPs substantially enhances root content and fresh weight in eggplants, compared to untreated eggplant. Elmer [33] demonstrated that CuONP-treated plants produced and yielded 39% more fruit than the untreated controls. Furthermore, the administration of Cu-NPs aided mung bean roots and shoot growth. According to Yasmine et al. [69], when wheat was treated with 25 ppm Cu-NPs, the spike length of wheat climbed slowly or remained unchanged, while the number of grains increased dramatically.
Copper compounds have been successful in the control of crop diseases caused by certain fungi and bacteria, as their cost is low and the risks of emergence of resistant strains of pathogens to these compounds are few or low, due to these compounds having more than one site of toxic action [70]. Particularly, copper nanoparticles cause a change in protein expression, which is the key to inhibiting microbial growth [71]. Although silver compounds have the same toxicity as copper compounds on plant pathogens, Cu 2 ONPs are more beneficial for use in the agricultural environment because they are less toxic than AgNPs. Cu 2 ONPs also have numerous modes of inhibitory action for microbial diseases [72], allowing them to be used as an alternative to chemical fungicides to control a variety of plant pathogens that infect plants. This would be extremely useful in decreasing the negative effects of fungicides, particularly on edible plants and fresh vegetables [73]. We also hope, in the future, to increase the study of this compound in terms of toxicity and the adoption of international companies and for it to reach the final product for its application at the field level among farmers.

Conclusions
Cu 2 ONPs inhibited the growth of F. solani in the laboratory, and they also reduced the disease incidence of the pathogen that causes cucumber root rot under greenhouse and field environments. They also improved cucumber growth and production characteristics. Defense enzyme activity and defense genes were expressed at higher levels in the cucumber plants treated with Cu 2 ONPs than in the untreated control. In comparison to the untreated plants, scanning electron microscopy and the anatomical investigation indicated anomalies, alterations, twisting in the mycelia, diminishing spores, and the collapse of F. solani, as well as increased cell wall, root cortex, and mesophyll tissue (MT) thickness of the cucumber plants.