Next Article in Journal
Optimization Design of a Pneumatic Wheat-Shooting Device Based on Numerical Simulation and Field Test in Rice–Wheat Rotation Areas
Next Article in Special Issue
Use of Lentinan and Fluopimomide to Control Cotton Seedling Damping-Off Disease Caused by Rhizoctonia solani
Previous Article in Journal
Dietary Resveratrol Alleviates AFB1-Induced Ileum Damage in Ducks via the Nrf2 and NF-κB/NLRP3 Signaling Pathways and CYP1A1/2 Expressions
Previous Article in Special Issue
The Role of Insect Cytochrome P450s in Mediating Insecticide Resistance
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

A Polysaccharide of Ganoderma lucidum Enhances Antifungal Activity of Chemical Fungicides against Soil-Borne Diseases of Wheat and Maize by Induced Resistance

1
Department of Plant Protection, Shandong Agricultural University, Tai’an 271018, China
2
Key Laboratory of Tobacco Pest Monitoring Controlling & Integrated Management, Tobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao 266101, China
3
Zhaoyuan Agro-Tech Extension Center, Yantai 265400, China
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Agriculture 2022, 12(1), 55; https://doi.org/10.3390/agriculture12010055
Submission received: 23 November 2021 / Revised: 28 December 2021 / Accepted: 28 December 2021 / Published: 2 January 2022
(This article belongs to the Special Issue Sustainable Use of Pesticides)

Abstract

:
Ganoderma lucidum polysaccharide (GLP), which is the primary active ingredient in G. lucidum, has been widely used in functional food and clinical medicine. However, it is rarely reported in the prevention and control of plant diseases. In this study, we found that the GLP can increase the germination rates and seedling heights of maize and wheat. We also found that the combination of GLP and chemical fungicides as a seed coating chemical compound has a control effect of more than 75% on the primary soil-borne diseases of the wheat and maize growing areas in both greenhouse and field trials. Furthermore, the combination of GLP and chemical fungicides prolongs the lasting period and reduces the application dosage of the chemical fungicides by half. In addition, GLP seed dressing could increase the resistance-related gene expression of the TPS and WRKY53 in maize and WMS533, NbPR1a, and RS33 in wheat. The combination of GLP and low-dose chemical fungicides proved to be an effective way to effectively prevent wheat sharp eyespot, root rot, and maize stalk rot in the wheat and maize continuous cropping areas in the North China Plain and to reduce pesticide use and increase crop yield.

1. Introduction

The North China Plain is an important grain production base in China. The annual production of maize and wheat accounts for approximately 40% and 60% of China’s total output, respectively. Therefore, it is also referred as China’s bread basket [1]. However, with the change in climate and the popularization of returning straw to the soil, soil-borne diseases, such as wheat sharp eyespot, wheat root rot, and maize stalk rot in wheat and maize rotation regions has increased yearly and seriously threatened crop yield and quality [2,3,4,5]. The pathogens of the three diseases can live through the winter through mycelium attached to the remnants of the diseased plant. In addition, the mycelium of wheat sheath blight and root rot can also live through the winter in the soil and inside and outside the seeds, respectively. Wheat sharp eyespot caused by Rhizoctonia cerealis van der Hoeven and root rot by Bipolaris sorokiniana are important typical soil-borne diseases threatening wheat production worldwide [6]. Wheat sharp eyespot can infect the stems and sheaths of wheat plants, leading to a block in nutrient transportation. Sharp eyespot is common in China, New Zealand, the United States, and other places, and has become an important disease on wheat. The yield loss and quality reduction caused by this disease exceeded $15 million per year in China [7]. Wheat root rot causes black lesions on the roots and bases and white heads that could even have empty spikes, resulting in a serious loss of wheat yield [8,9]. Maize stalk rot caused by Fusarium graminearum is a systemic soil-borne disease that seriously damages maize production [10]. Its outbreak is sudden and dramatic, which can directly affect the absorption of water and nutrients in maize plants and destruct their metabolic function, thus causing serious losses in maize yield and quality [11,12,13].
Traditionally, the management of soil-borne diseases primarily depends on disease-resistant breeding and chemical agents [14,15]. However, the current agronomic practices are not sufficiently effective, and breeding resistant varieties is time consuming [16]. In addition, research on the use of pesticides in the production of maize and wheat in China has shown that the increased use of pesticides in agriculture results in adverse effects on human and animal health, environmental pollution in water and soil, and side effects on beneficial organisms, including pollinators, decomposers, and natural enemies [17]. In recent years, the increased use of EBIs (ergosterol biosynthesis inhebitors, EBIs), particularly the azole antifungals, has resulted in the development of drug resistance, and there is cross-resistance between the agents [18,19]. The repeated application had also brought about a serious problem of pesticide resistance. Fungicides in the soil could also affect subsequent crop growth through winter wheat seed dressing experiments [20]. Zaller reported that fungicidal seed dressings could increase the number of protozoa, reduce the plant decomposition rate, and affect soil microbial activity [21]. China has implemented a strategic target for pesticide reduction [22]. It focused on how to reduce the use dosage of pesticides, find environmentally friendly alternatives, and safeguard crop production [23]. The use of immune inducers to protect plants against pests by activating host resistance has become a research hotspot in recent years.
Ganoderma lucidum is a basidiomycetes polyporaceous fungus that contains many types of bioactive components, of which the key components are G. lucidum polysaccharide (GLP) [24,25]. Its primary structural feature is a β-1,3-D-linear, which is consistent with many reported structures of fungal polysaccharides, and belongs to the β-1,3-glucans (Figure 1) [26]. The main chain structure of polysaccharides is β-(1→3)-linked d-glucopyranose residue, and the side chain is linked with single, disaccharide, and oligosaccharide at the C-6 position of the main chain. GLP has been used to prevent intestinal disorders and obesity-related metabolic disorders in obese individuals, regulate insulin production, and inhibit cancer cell growth [27,28,29]. However, the application prospects of GLP in agriculture are not clear. In this study, we evaluated the prevention and control effects of GLP and chemical agents combined with reduced dosage on three soil-borne diseases in greenhouse and field trials. The purpose is to study the control effect of GLP on the main soil-borne diseases in the wheat and maize rotation areas in the North China Plain and to explore the possibility of reducing the use of chemicals by inducing plant disease resistance, so as to provide references for the wide application of GLP in disease control and providing a basis for evaluation of biopesticide efficacy.

2. Materials and Methods

2.1. Fungal Isolates, Culture Media, Fungicides and Varieties Tested

The strains used in this study, R. cerealis, B. sorokiniana, and F. graminearum, were all provided by the Microbe Provincial Key Laboratory of Shandong Agricultural University and used after activation and purification steps. They were cultivated in potato dextrose agar (PDA) media (200 g potato, 20 g dextrose and 20 g agar per 1 L). The liquid media excluded agar.
The fungicides used, difenoconazole (96%), fludioxonil (98%), prochloraz (97%), thiram (96%), hexaconazole (95%), metalaxyl (98%), and fluopimomide (98%) were all technical grade. Stock solutions (1 × 104 μg/mL) were prepared in acetone and stored at 4 °C.
The wheat cultivated varieties tested included Shannong 23, Jimai 22 and Luyuan 502. The maize cultivated varieties tested included Zhengdan 958, Xianyu 335 and Luning 202. These cultivated varieties are widely planted in the wheat and maize areas of the North China Plain.

2.2. Extraction and Purification of GLP

Fruiting bodies of G. lucidum were obtained from the Jiangsu Alphay Biological Technology Co., Ltd. (Nantong, China). GLP was obtained using water extraction and alcohol precipitation. The Ganoderma lucidum fruiting body was dried at 50 °C and crushed, and 95% ethanol was used to remove impurities and small lipophilic molecules for 24 h. The solution was degreased with petroleum ether and extracted with distilled water at 80 °C for 8–10 h in several batches. The filtered residue was extracted three times. The extraction solution was mixed, and vacuum concentration was performed. The polysaccharides (crude polysaccharides) were precipitated again with ethanol. The precipitate obtained was lyophilized and combined. (Figure 2) After quantified with the phenol–sulfuric acid method [30], the extraction rate of GLP (w/w) was 25.8%.

2.3. Fungicide Amended-Agar Assay

Gradient dilutions of the chemical fungicides (difenoconazole, fludioxonil, prochloraz, thiram, hexaconazol, metalaxyl, and fluopimomide) and GLP were conducted with acetone and sterile water at an ultra-clean bench; acetone control was used as a control. 1 mL of each diluted solution was mixed with 49 mL of sterilized PDA medium before pouring in plates. A 7 mm mycelial plug cut from the edge of the activated strain was inoculated in the center of each PDA plate. Each treatment was repeated three times, and the culture was grown at 25 °C in dark. When the colony diameter of the control group reached approximately 70 mm, the diameter of the colonies was determined using the cross method (measuring the colony diameter in two vertical directions), and the average value was used to calculate the inhibition rate (%) of each concentration of the agent [31]. The data obtained were analyzed using SPSS 22.0 to calculate the EC50 value of the agent against various pathogens.

2.4. Effects of GLP Seed Dressing on Wheat and Maize Germination and Seedling Growth

Maize and wheat seeds were surface-disinfected for 3 min in 1% (w/v) NaOCl followed by 3 min in 70% (v/v) ethanol and rinsed three times in sterile distilled water before the experiment. Wheat germination and seedling growth were conducted as described by Zhang [4].
The main components of seed coating are as follows: Fungicides (1) 4% GLP, (2) 8% GLP, (3) 0.5% hexaconazole, (4) 1% hexaconazole, (5) 2% hexaconazole, (6) 4% GLP + 0.5% hexaconazole, (7) 15% GLP, (8) 30% GLP, (9) 20% prochloraz, (10) 40% prochloraz, (11) 80% prochloraz, (12) 15% GLP + 20% prochloraz), 3.1% BY140, 4% NNO, 3% Polyacrylamide + CMC, 4% Ethylene glycol, 0.2% Gelatin, 6% Pigment red, and water is used to make up 100%.
In all tests, the coating agent was applied at doses of 100 mL per 100 kg of seeds. The wheat seeds were subjected to 7 treatments: (1) 4% GLP; (2) 8% GLP; (3) 0.5% hexaconazole; (4) 1% hexaconazole; (5) 2% hexaconazole; (6) 4% GLP + 0.5% hexaconazole, and (7) sterile water treatment (control).
The maize seeds were subjected to the following 7 treatments: (1) 15% GLP; (2) 30% GLP; (3) 20% prochloraz; (4) 40% prochloraz; (5) 80% prochloraz; (6) 15% GLP + 20% prochloraz, and (7) sterile water treatment (control).

2.5. Effects of GLP on Wheat Sharp Eyespot, Wheat Root Rot and Maize Stem Rot

The seed treatment in this experiment is completely consistent with the above-mentioned treatments of wheat and corn seed germination and seedling growth, except that the highest dose of fungicide treatment is removed. Then we coated seeds (100 kg) with different doses of GLP or fungicide or the same volume of sterile water (control). The treated seeds are used after being dried in the air. The soil was collected from fields infested with wheat sharp eyespot, root rot and maize stem rot and filled in plastic pots with a diameter of approximately 30 cm. Then each pot received 20 mL of pathogenic bacteria (R. cerealis, D. sorokiniana and F. graminearum) suspension (OD420 = 0.56), and 10 treated seeds were sown in. It was cultured in a greenhouse with temperature of 20 ± 2 °C, relative humidity of 70 ± 5%, and light-dark ratio (L:D) = 14:10. Each pot was one replicate, and each treatment was repeated three times.
The disease incidence and severity in each treatment were investigated at 7 d, 14 d and 21 d after seedlings sprout. The classification criteria of wheat sharp eyespot disease are as follows [32]: grade 0, no onset; grade 1, leaf-based point-like disease; grade 3, lesion circle ring stem less than 1/2; grade 5, stem-based lesions more than 1/2; and grade 7, dead, lodging. The wheat root rot classification criteria were as follows: 0, no visible lesions; level 1, local sensation of the stem base, brown small lesions, light color; level 2, deep brown spots visible at the base of the stem and visible lesions. The width is 1/5 or less of the circumference of the base of the stem; level 3, the lesion at the base of the stem is connected to the growth strip, and the width of the lesion is less than 1/3 of the circumference of the base of the stem, which has an influence on yield; level 4, the lesion is 1/2 or less of the circumference of the base of the stem, which has a heavier effect on the yield, and at level 5, the lesion at the base of the stem is more than 3/5 of the circumference of the base of the stem, which has a serious impact on the yield. The grading criteria of maize stem rot disease were as follows: 0 indicated healthy plants with a well-developed root and coleoptile; 1 indicated plants with 25% of the radicle and coleoptile exhibiting decay symptoms; 2 indicated >25% to 50% of the radicle and coleoptile exhibiting decay symptoms; 3 indicated >50 to 75% of the radicle and coleoptile exhibiting decay symptoms; and 4 indicated radicles and coleoptiles with ≥75% decay. The disease severity index (%) and the control effect (%) of each treatment were calculated according to the formulas (1) and (2), respectively [13,33,34].
Disease severity index = [∑ (number of diseased plants with a certain index value × index value)/(total number of plants investigated × highest disease index)] × 100%.
Control = [(disease severity index in the control group − disease severity index in the treated group)/disease severity index in the control group] × 100%.

2.6. Field Trials

Field tests of efficacy were conducted in the experimental field of Taian, Shandong, China (36.17° N, 117.17° E) from 2017 to 2019. This area belongs to temperate monsoon climate zone with moderate rainfall, annual average temperature is about 13 °C and annual average precipitation is about 670 mm. It belongs to fertile brown soil. Due to long-term wheat and maize rotation, wheat sharp eyespot, wheat root rot, and maize stem rot are severe in this region. The experimental field for each treatment covered 150 m2 with three replications. Maize plants at the test site were planted each year on approximately 5 June. We investigated the incidence of maize stalk rot and its control effect each year on 30 July and 20 August. Wheat was planted in the autumn after the seed dressing treatment, and the incidence and control effect of wheat sharp eyespot were investigated in the wintering, jointing and filling stages of the wheat. The control effect of wheat root rot was examined at the wheat seedling stage.

2.7. RNA Extraction and Real-Time Quantitative RT-PCR

Leaves of maize grown from seeds exposed to 15% and 30% GLP and wheat grown from seeds exposed to 4% and 8% GLP was collected 7 d after seedling emergence and stored at −80 °C. Total RNA was extracted using Plant Total RNA Kits (Omega, Norcross, GA, USA) according to the manufacturer’s instructions. First-strand cDNA was synthesized using a RevertAid First Strand cDNA Synthesis Kit (ThermoFisher Scientific, Waltham, MA, USA). The qRT-PCR reactions were performed in triplicate on each of three replicates. The qRT-PCR was performed on a Quantitative PCR Q6 Thermal Cycler (ABI, Carlsbad, CA, USA) using a SYBR Green-based PCR reaction mixture and 8 ng template cDNA. Specific primers were designed using the Primer Express software (Sandon Biotech, Shanghai, China) (Table 1).

2.8. Data Processing and Analysis

In this paper, in fungicide amended-agar assay, the percentage of inhibition were calculated using the following excel formula, and the half maximal effective concentration (EC50) values was determined by the one-way ANOVA log-probability regression analysis of SPSS 22.0 software.
Inhibition growth (%) = (Diameter of fungal hyphae colony in the control − Diameter of fungal hyphae colony under fungicide effect)/Diameter of fungal hyphae colony in the control) × 100
The test data of diameter of fungal hyphae, greenhouse and field were subjected to the Shapiro–Wilk’s and Levene’s tests (p > 0.05) to confirm normal distribution and homoscedasticity, and statistically analyzed by Duncan’s new complex range method (DMRT) of different treatments, and the test results were evaluated (p < 0.05).

3. Results

3.1. In Vivo Assays Test of GLP and Fungicides against Fusarium graminearum, Drechslera sorokiniana and Rhizoctonia cerealis

The results indicated that prochloraz, fludioxonil and hexaconazole had higher toxicity than metalaxyl and fluopimomide on the hyphal growth of F. graminearum. The fungicidal effect of prochloraz was best with EC50 value 0.088 mg·L−1 (Table 2). Hexaconazole, prochloraz and fludioxonil had higher toxicity than the other treatment on the hyphal growth of D. sorokiniana, with EC50 values all lower than 1.0 mg·L−1. Hexaconazole had the strongest fungicidal effect, and its EC50 value is only 0.144 mg·L−1 (Table 3). Hexaconazole and fludioxonil had higher toxicity on the hyphal growth of R. cerealis, with EC50 values of 0.094 mg·L−1 and 0.312 mg·L−1, respectively (Table 4). In addition, GLP, a biological resistance-inducing agent, showed no direct fungicidal effect on these pathogens.

3.2. Effects of Seed Dressing on Wheat and Maize Germination

It can be seen from Table 5 that the germination rate of wheat seeds treated with GLP was higher than that of the control, while the germination rate of wheat seeds treated with hexaconazole was significantly lower than that of the control. The difference is that there is no significant difference in the germination rate with different doses of GLP treatment, while the germination rate decreases with the increase of the hexaconazole dose. Three days after complete germination, the germination rate of the seeds treated with each dose of hexaconazole was equal to that of the control, indicating that the inhibitory effect of high-dose hexaconazole on germination can be quickly restored. And the combination of GLP and hexaconazole has no significant difference compared with the control, indicating that the compound GLP can alleviate the inhibitory effect of low-dose hexaconazole on germination. In addition, from the numerical point of view, there is no significant difference in the effect of each treatment on the germination rate of different cultivated varieties of wheat.
The results in Table 6 indicated that the germination rate of Zhengdan 958, Xianyu 335 and Luning 202 treated with GLP is higher than 50% when the control germination is 50%, but the induction effect has no significant increase with the treatment dose. Fungicide prochloraz showed a slight decrease in the germination rate of the three cultivated varieties of maize seeds compared with the control. When the control was completely germinated, the three cultivated varieties of maize seeds treated with 40% and 80% prochloraz were lower than the control, and the higher the treatment dose, the lower the germination rate. Therefore, prochloraz has an inhibitory effect on the early germination of maize, and its effect on Xianyu 335 is the most obvious. Three days after the complete germination, the germination rates of the three cultivated varieties of maize seeds treated with GLP and prochloraz were the same as the control. This indicated that the inhibitory effect of prochloraz on the germination of the maize seeds was temporary, and it had no effect on the final emergence rate of each cultivated variety. After treatment of wheat seeds with 20% prochloraz and 15% GLP, the germination rate of the three cultivated varieties of maize was not significantly different with the control.

3.3. Effects of Seed Dressing on the Growth of Wheat and Maize Seedlings

The effect of the GLP on the promotion of the wheat seedling growth and the inhibitory effect of hexaconazole on the plant height of the wheat were more significant in the early stage (Table 7). 7 d after emergence, the plant heights of the three wheat cultivars treated with at 4% g and 8% GLP were significantly higher than the control, and the effect of induction increased in parallel with the treatment dose. The plant height of the three cultivated varieties treated with 0.5%, 1% and 2% hexaconazole was lower than that of the control, and the significance of the inhibition increased in parallel with the dose of the drug, particularly in Jimai 22. The performance of Luyuan 502 on these two cultivated varieties is more pronounced. After treatment with 0.5% hexaconazole and 4% GLP, the plant heights of the three cultivated varieties were 7.22, 6.52 and 7.44 cm, respectively. They were significantly higher than the single dose of hexaconazole. This shows that when the bioinhibitor GLP and hexaconazole are used in combination for seed treatment, it can alleviate the seedling growth inhibition of the triazole fungicides. On the 21st day after emergence, the induction of GLP and the inhibition of hexaconazole were lower than those of the first two determination periods, and the difference between the treatments was significantly reduced, but the high dose of fungicide treatment still had a significant effect on the wheat plant height with the effect on Jimai 22 and Luyuan 502 more pronounced.
Seven days after the emergence of maize, the plant heights of Zhengdan 958, Xianyu 335 and Luning 202 treated with 15% GLP were 7.88, 7.50 and 6.48 cm, respectively, which were significantly higher than the control of 7.23, 6.52 and 5.36 cm. The induction effect of 30% GLP treatment was more pronounced. Treatment of the three cultivated varieties of maize seeds with 20%, 40%, and 80% prochloraz had no effect on maize plant height. Seed treatment with 20% prochloraz and 15% GLP resulted in a plant height of maize that was significantly higher than that of the control and the same dose of prochloraz. On the 21st day after emergence, the difference in plant height between the treatments was reduced. There was no significant difference in the plant height of each dose of GLP and prochloraz-treated Zhengdan 958. The only significant difference observed was from the 30% GLP treatment. The height of the treated Xianyu 335 was significantly higher than that of the control, and there was no significant difference between the other treatments (Table 8).

3.4. Control Effect of The Seed Treatment on 3 Soil-Borne Diseases in Wheat and Maize Continuous Cropping Areas

As seen results in Table 9, the greenhouse control effects of hexaconazole on wheat sharp eyespot increased with the treatment dose. The treatments of Jimai 22, Shannong 23 and Luyuan 502 with 1% hexaconazole treatment, and the control effects on sharp eyespot on the 7 days after the emergence of wheat were 79.7%, 72.0% and 77.3%, respectively. The bioinducing agent GLP was used alone, although the greenhouse effect of the wheat sharp eyespot increased with the treatment dose, but the direct induction effect was still low. The combination of the fungicides and bioinducing agents for wheat seed treatment is much more effective against wheat sharp eyespot than a single agent treatment. After the seed dressing of 0.5% hexaconazole and 4% GLP, the control effects on the three cultivated varieties were 75.8%, 67.1% and 73.4%, respectively. The control effect was not significantly different from the 1% hexaconazole treatment. The 21 d control effect of Shannong 23 was 65.2%, which was 8.9% higher than that of 1% hexaconazole. The treatment group of 1% hexaconazole effectively controlled the wheat root rot, and the control effects on the 7 d of the three cultivated varieties are 76.3%, 80.2% and 80.4%, respectively (Table 10). The 21 d control effects still reached 55.3%, 68.6% and 65.4%. The bioinhibitor GLP was used alone to treat the wheat seed, and its effect on the root rot was minimal, respectively. The control effect of the bioinducing agent GLP and the fungicide hexaconazole mixed seed dressing was significantly higher than the single agent treatment. 0.5% hexaconazole and 4% GLP were mixed, and the 7 d control effects on the three cultivated varieties were 79.4%, 82.6% and 81.5%, respectively. The 21 d control effects were 61.5%, 74.9% and 67.1%, respectively. Both were significantly higher than the 0.5% hexaconazole seed dressing.
Zhengdan 958, Xianyu 335 and Luning 202 were treated with 40% prochloraz, the 7 d control effects on the maize stem rot were 88.8%, 82.9% and 76.2%, respectively (Table 11). The 21 d control effects were down to 60.6%, 65.2% and 56.2%. The control efficiency of three maize varieties was less than 40% when treated with biological inhibitor GLP alone. 20% prochloraz and 15% GLP were applied to the seeds of the three cultivated varieties. The 7-day control effect of the disease was 84.2%, 80.8% and 73.7%, respectively, significantly lower than the 40% prochloraz. However, the control effect after 21 days was still 67.9%, 65.1% and 61.9%, respectively, and the duration of effect was longer.

3.5. Field Control Effect of Seed Treated on Wheat Sharp Eyespot, Wheat Root Rot and Maize Stalk Rot

Field trials performed through two years demonstrated that all treatments reduced disease severity and provided substantial disease control. We observed that the use of GLP seed dressing had a weak effect on wheat sharp eyespot and wheat root rot, which was approximately 35%. The field control effects of the hexaconazole seed dressing on wheat sharp eyespot and wheat root rot in the early stage of wheat growth was approximately 80%. However, with the gradual reduction of the chemical agent alone over time. The combination of the GLP and a relatively low dose of hexaconazole provided good control of wheat sharp eyespot, and it has a long period of validity. The control effect on wheat sharp eyespot in the early winter wheat period is greater than 77%. In the wheat filling stage, the effect of the combined seed dressing on the sharp eyespot is still more than 40%, which is higher than the double dose of hexaconazole seed dressing (Table 12).
GLP treatment of maize stalk rot in the field indicated that the GLP treatment has effects on maize stalk rot. For example, the effect of high-dose prochloraz on maize stalk rot was 76~82% on 30 July 2017 and 30 July 2018. On 20 August, the effect of prochloraz on maize stalk rot was approximately 60%. With the passing of time, the effect of prochloraz on the control of maize stem rot was significantly reduced by 21.1~26.8%. A low-dose combination of prochloraz and Ganoderma lucidum is highly effective at controlling maize stem rot, and its effect is not significantly different from the high dose of prochloraz. In summary, GLP has broad application prospects to prevent and control maize diseases (Table 13).

3.6. Effects of Chemical Seed Treatment on the Yield of Wheat and Maize

After two years of field experiments, we concluded that the yield of wheat and maize could be improved by the combination of the GLP polysaccharide, the chemical fungicides and the combination of the two treatments. The effect of the GLP seed dressing alone on yield was less than that of chemical agent, while the combination of GLP and a low dose of fungicide could significantly increase crop yield and had more pronounced effects on the yield of wheat. 0.5% GLP and 4% prochloraz were combined to treat the wheat seed of the cultivars Jimai 22, Shannon 23 and Luyuan 502. In 2017 and 2018, the yield was 7692.84 and 7128.60, 7910.40 and 6979.35, and 7722.90 and 6535.20 kg·hm−2, respectively. These values were significantly higher than those of the other treatments (Table 14).

3.7. Effect of Seed Treated GLP on Transcript Quantity of Wheat and Maize Disease Resistance-Related Gene

The relative expression level of the broad-spectrum disease resistance-related gene WMS533, resistance to sharp eyespot gene Xwmc364, and the resistance to sharp eyespot related gene RS33 after treatment with 4% GLP was 3.9, 4.5, and 5.8, respectively. 8% GLP-treated of the mitogen-activated protein (MAP) kinase analog gene IR6, the broad-spectrum disease-resistant gene WMS533, resistance to sharp eyespot gene-linked primer Xwmc364, the relative expression levels of the gene NbPR1a and the wheat sharp eyespot resistance gene RS33 were 5.3, 5.8, 3.7, 5.1 and 6.9, respectively, indicating a high level. Different doses of GLP seed dressing have different effects on the expression of resistance genes related to Jimai 22. In general, GLP can induce the expression of the broad-spectrum disease resistant-related gene WMS533 and wheat resistance to the wheat sharp eyespot-related gene RS33. The amount is also significantly increased as the treatment dose is increased. In addition, a high dose of GLP can significantly induce the expression of the mitogen-activated protein (MAP) kinase analog gene IR6 and the pathogenesis-related gene NbPR1a, which may be more significant at inducing wheat resistance to wheat with the high dose of GLP. There is a close relationship between the diseases (Figure 3).
Leaf tissue from 15% and 30% GLP-treated maize seedlings was collected to investigate the expression of resistance-related genes in maize seedlings. The results showed that maize treated with GLP had the greatest influence on the TPS and WRKY53 genes in Zhengdan 958. After seed dressing by 15% and 30% GLP, the relative expression of the TPS and WRKY53 genes was 3.5 and 6.2, and 5.3 and 6.8, respectively. We also detected an increase in the expression levels of genes such as CHITc, TPS21, TPC, and JAR1 (Figure 4).

4. Discussion

The North China Plain is an important grain producing area in China, and the primary planting method is winter wheat and summer maize [35]. Wheat sharp eyespot, which is primarily caused by R. cerealis, wheat root rot, which is primarily caused by D. sorokiniana, and maize stalk rot, which is primarily caused by F. graminearum, are systemic soil-borne diseases that seriously endanger the production of wheat and maize [11,12,36].
Hexaconazole is a triazole fungicide widely used internationally due to its wide spectrum of sterilization and low risk of drug resistance [37]. It is effective at controlling wheat scab and is widely used. Prochloraz is a popular imidazole fungicide that inhibits the biosynthesis of ergosterol, which is part of the cell membrane in many fungi [38]. Due to its high biological activity against F. verticillioides, prochloraz is used as a foliar spray to control maize diseases in the major maize producing regions in China. Our previous research reported a (1~3) β-D-glucan, which can induce the activity of protective enzymes, increase the content of chlorophyll, induce the gene expression of the salicylic acid pathway and act as a broad-spectrum resistance-related pathway to induce resistance against wheat sharp eyespot [32].
Throughout this experiment, we concluded that hexaconazole has strong antifungal effects on wheat sharp eyespot and wheat root rot, and prochloraz is more effective against the maize stem rot pathogen. The seed treatment of the two pesticides has a good control effect on the soil-borne diseases in the seedling stage of plants. Meanwhile, we concluded that the GLP can increase the germination rates and seedling heights of maize and wheat, and exists in all three selected cultivated varieties. When GLP is combined with fungicides to treat wheat and maize seeds, this promotion still exists.
Interestingly, we concluded that GLP does not have any antifungal activity against soil-borne fungi. However, when the seeds are treated with GLP, they can control the soil-borne diseases by approximately 35% in greenhouse potting and field control experiments. Previous studies demonstrated that biological elicitors could control plant diseases by stimulating plants disease resistance, even if they have no obvious fungicidal effect [39]. When the plants are stimulated by biological agonists, they usually change factors, such as the deposition of callose, the synthesis of defense enzymes, reinforcement of the plant cell wall associated with phenyl propanoid compounds, and the accumulation of pathogenesis-related (PR) proteins to protect against pests and diseases [40]. There were reports that seaweed polysaccharides, such as ulvans, alginates, fucans, laminarin, carrageenans, and their derived oligosaccharides, can induce an initial oxidative burst and the activation of SA, JA and/or ethylene signaling pathways in terrestrial plants [1,41]. The activation of these signaling pathways leads to an increase in the expression of PR proteins that have antifungal and antibacterial activities and lead to an increased expression of defense enzymes that participate in the synthesis of PPCs, terpenes, terpenoids and alkaloids with antimicrobial activities [42].
Therefore, we hypothesize that GLP increases resistance to maize stalk rot by affecting the expression of the TPS and WRKY53 genes in maize. GLP achieves resistance to wheat sharp eyespot and wheat root rot by increasing the relative expression of the broad-spectrum disease resistance-related gene WMS533, the disease-related gene NbPR1a, and the wheat resistance-resistance related gene RS33.
Combined with greenhouse pot and field control experiments, we concluded that the effect of GLP alone on wheat sharp eyespot, wheat root rot, and maize stem rot is approximately 35%. It is lower than the control effect of the chemical fungicides hexaconazole and prochloraz. However, we concluded that GLP seed dressing enhances the control effect of the chemical fungicides. When GLP is combined with low-dose hexaconazole or prochloraz in the treatment of wheat or maize seeds, the effect of prevention and control of soil-borne diseases in the early stage of paper growth is approximately 70%, the same degree of control that results from twice the dose of hexaconazole or prochloraz. Over time, the combination of the GLP and low-dose fungicides effectively controls wheat sharp eyespot and maize stem rot, even more than the control effect of the double dose of hexaconazole and prochloraz.
This has strong implications for reducing the use of pesticides. The increase in the dose of the pesticide and the increasing frequency of the use of pesticides leads to the increasing drug resistance of pathogens, resulting in a vicious cycle of increasing drug consumption and plant diseases [43]. GLP can help to solve this problem. First, GLP combined with chemical seed dressings effectively simultaneously prevented plant diseases and reduced the dose of chemicals. Second, GLP and chemical combined seed dressings prolonged the control period, thus reducing the frequency of the use of chemical pesticides. Biological inducers can induce disease resistance in plants, but the control effect on diseases is between 20% and 80% [39]. In many cases, bioinducing agents are less effective at controlling diseases than chemical fungicides. The combination of fungicides and bioinducing agents can enhance the control effect on diseases. The reasons for this are two-fold. First, it takes a certain time for the bioinducing agent to induce disease resistance in the plants. Conventional fungicides can inhibit the growth of pathogenic fungi before the plants develop disease resistance. Second, chemical fungicides have been found very effective in reducing the pathogenicity of the pathogenic fungi [44]. The ability to induce resistance in plants makes it easier to control pathogens, and therefore, reduces the amount of chemical fungicides used and the number of uses [45].
In addition, we found that GLP combined with fungicide can increase crop yield. Field results in 2017 showed that the yield of the combined application of fungicides and GLP by half was equivalent to that of fungicides and GLP, and both were significantly higher than the control. The 2018 results were basically the same as 2017. Only the combined treatment of Xianyu 336 (maize cultivated variety) was significantly higher than the GLP treatment, and the combined treatment of Jimai 22 (wheat cultivated variety) was higher than the fungicide treatment. These findings are consistent with those of Naz, et al., who reported that botanical-chemical formulations protected against B. sorokiniana and enhanced yield in wheat. We speculate that this is due to the fact that GLP promotes plant health and is combined with fungicides to improve disease prevention effects. In addition, in field trials, we also found that maize rough dwarf virus and maize dwarf mosaic virus were less susceptible to GLP seed dressing plots.

5. Conclusions

In short, we studied the control effects of GLP on three soil-borne diseases in wheat and maize rotation region of North China Plain through the greenhouse and in a field trial, and found that GLP could induce resistance of wheat and maize to soil-borne diseases. GLP seed mixing could reduce pesticide dosage and increase crop yield. Based on previous studies, we hypothesized that GLP improves disease resistance by affecting the expression of related genes in maize and wheat. These results provide a reference for the wide application of GLP in disease prevention and treatment.

Author Contributions

Conceptualization, H.W.; methodology, J.W. and H.W.; software, S.S.; formal analysis, X.Y., Z.Z. and Y.L.; investigation, Q.C. and Z.Z.; data curation, X.Y. and S.S.; writing—original draft, X.Y. and H.W.; writing—review and editing, H.W.; funding acquisition, H.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Major Science and Technology Innovation Project of Shandong Province (2019JZZY020608), the National Natural Science Foundation of China (32102259) and the Special Fund for Agro-scientific Research in the Public Interest of China (No. 201503130).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data that support the findings of this study are available from the corresponding authors upon reasonable request.

Conflicts of Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

References

  1. Mercier, L.; Lafitte, C.; Borderies, G.; Briand, X.; Esquerré-Tugayé, M.T.; Fournier, J. The Algal Polysaccharide Carrageenans Can Act as an Elicitor of Plant Defence. New Phytol. 2010, 149, 43–51. [Google Scholar] [CrossRef]
  2. Presello, D.A.; Botta, G.; Iglesias, J.; EyhéRabide, G.H. Effect of disease severity on yield and grain fumonisin concentration of maize hybrids inoculated with Fusarium verticillioides. Crop Prot. 2008, 27, 572–576. [Google Scholar] [CrossRef]
  3. Piao, S.; Ciais, P.; Huang, Y.; Shen, Z.; Peng, S.; Li, J.; Zhou, L.; Liu, H.; Ma, Y.; Ding, Y. The impacts of climate change on water resources and agriculture in China. Nature 2011, 467, 43–51. [Google Scholar] [CrossRef]
  4. Zhang, P.; Zhang, J.; Chen, M. Economic impacts of climate change on agriculture: The importance of additional climatic variables other than temperature and precipitation. J. Environ. Econ. Manag. 2017, 83, 8–31. [Google Scholar] [CrossRef]
  5. Li, H.; Dai, M.; Dai, S.; Dong, X. Current status and environment impact of direct straw return in China’s cropland—A review. Ecotox. Environ. Safe 2018, 159, 293–300. [Google Scholar] [CrossRef] [PubMed]
  6. Ren, X.-X.; Chen, C.; Ye, Z.-H.; Su, X.-Y.; Xiao, J.-J.; Liao, M.; Cao, H.-Q. Development and Application of Seed Coating Agent for the Control of Major Soil-Borne Diseases Infecting Wheat. Agronomy 2019, 9, 413. [Google Scholar] [CrossRef] [Green Version]
  7. Liu, J.; Mundt, C.C. Genetic structure and population diversity in the wheat sharp eyespot pathogen Rhizoctonia cerealis in the Willamette Valley, Oregon, USA. Plant Pathol. 2020, 69, 101–111. [Google Scholar] [CrossRef]
  8. Daval, S.; Lebreton, L.; Gazengel, K.; Boutin, M.; Guillermerckelboudt, A.Y.; Sarniguet, A. The biocontrol bacterium Pseudomonas fluorescens Pf29Arp strain affects the pathogenesis-related gene expression of the take-all fungus Gaeumannomyces graminis var. tritici on wheat roots. Mol. Plant Pathol. 2011, 12, 839. [Google Scholar] [CrossRef]
  9. Wang, A.; Wei, X.; Rong, W.; Dang, L.; Du, L.P.; Qi, L.; Xu, H.J.; Shao, Y.; Zhang, Z. GmPGIP3 enhanced resistance to both take-all and common root rot diseases in transgenic wheat. Funct. Integr. Genom. 2015, 15, 375–381. [Google Scholar] [CrossRef] [PubMed]
  10. Costa, R.V.d.; Simon, J.; Cota, L.V.; Silva, D.D.d.; Almeida, R.E.M.d.; Lanza, F.E.; Lago, B.C.; Pereira, A.A.; Campos, L.J.M.; Figueiredo, J.E.F. Yield losses in off-season corn crop due to stalk rot disease. Pesqui. Agropecu. Bras. 2019, 54, 00283. [Google Scholar] [CrossRef] [Green Version]
  11. Venturini, G.; Assante, G.; Toffolatti, S.L.; Vercesi, A. Mating behavior of a Northern Italian population of Fusarium verticillioides associated with maize. J. Appl. Genet. 2011, 52, 367–370. [Google Scholar] [CrossRef] [Green Version]
  12. Subedi, S.; Subedi, H.; Neupane, S. Status of maize stalk rot complex in western belts of Nepal and its integrated management. J. Maize Res. Dev. 2016, 2, 30–42. [Google Scholar] [CrossRef] [Green Version]
  13. Gai, X.T.; Xuan, Y.H.; Gao, Z.G. Diversity and pathogenicity of Fusarium graminearum species complex from maize stalk and ear rot strains in northeast China. Plant Pathol. 2017, 66, 1267–1275. [Google Scholar] [CrossRef]
  14. Yang, Q.; Yin, G.; Guo, Y.; Zhang, D.; Chen, S.; Xu, M. A major QTL for resistance to Gibberella stalk rot in maize. Theor. Appl. Genet. 2010, 121, 673–687. [Google Scholar] [CrossRef] [PubMed]
  15. Shin, J.H.; Han, J.H.; Ju, K.L.; Kim, K.S. Characterization of the Maize Stalk Rot Pathogens Fusarium subglutinans and F. temperatum and the Effect of Fungicides on Their Mycelial Growth and Colony Formation. Plant Pathol. J. 2014, 30, 397–406. [Google Scholar] [CrossRef] [Green Version]
  16. Song, F.J.; Xiao, M.G.; Duan, C.X.; Li, H.J.; Zhu, Z.D.; Liu, B.T.; Sun, S.L.; Wu, X.F.; Wang, X.M. Two genes conferring resistance to Pythium stalk rot in maize inbred line Qi319. Mol. Genet. Genom. 2015, 290, 1543–1549. [Google Scholar] [CrossRef] [PubMed]
  17. Zhang, C.; Hu, R.; Shi, G.; Jin, Y.; Robson, M.G.; Huang, X. Overuse or underuse? An observation of pesticide use in China. Sci. Total Environ. 2015, 538, 1–6. [Google Scholar] [CrossRef] [PubMed]
  18. Kunz, S.; Deising, H.B.; Mendgen, K. Acquisition of Resistance to Sterol Demethylation Inhibitors by Populations of Venturia inaequalis. Phytopathology 1997, 87, 1272–1278. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Song, Z.; Nes, W.D. Sterol Biosynthesis Inhibitors: Potential for Transition State Analogs and Mechanism-Based Inactivators Targeted at Sterol Methyltransferase. Lipids 2007, 42, 15–33. [Google Scholar] [CrossRef] [PubMed]
  20. Van, W.H.; Tiefenbacher, A.; König, N.; Dorn, V.M.; Hagenguth, J.F.; Prah, U.; Widhalm, T.; Wiklicky, V.; Koller, R.; Bonkowski, M. Single and Combined Effects of Pesticide Seed Dressings and Herbicides on Earthworms, Soil Microorganisms, and Litter Decomposition. Front. Plant Sci. 2017, 8, 215. [Google Scholar]
  21. Zaller, J.G.; König, N.; Tiefenbacher, A.; Muraoka, Y.; Querner, P.; Ratzenböck, A.; Bonkowski, M.; Koller, R. Pesticide seed dressings can affect the activity of various soil organisms and reduce decomposition of plant material. BMC Ecol. 2016, 16, 37. [Google Scholar] [CrossRef] [Green Version]
  22. Jin, S.; Zhou, F. Zero Growth of Chemical Fertilizer and Pesticide Use: China’s Objectives, Progress and Challenges. J. Resour. Ecol. 2018, 9, 50–58. [Google Scholar]
  23. Burketova, L.; Trda, L.; Ott, P.G.; Valentova, O. Bio-based resistance inducers for sustainable plant protection against pathogens. Biotechnol. Adv. 2015, 33, 994–1004. [Google Scholar] [CrossRef]
  24. Cao, Y.; Wu, S.H.; Dai, Y.C. Species clarification of the prize medicinal Ganoderma mushroom “Lingzhi”. Fungal Divers. 2012, 56, 49–62. [Google Scholar] [CrossRef]
  25. Habijanic, J.; Berovic, M.; Boh, B.; Plankl, M.; Wraber, B. Submerged cultivation of Ganoderma lucidum and the effects of its polysaccharides on the production of human cytokines TNF-α, IL-12, IFN-γ, IL-2, IL-4, IL-10 and IL-17. New Biotechnol. 2015, 32, 85–95. [Google Scholar] [CrossRef] [PubMed]
  26. Sasaki, T.; Takasuka, N. Further study of the structure of lentinan, an anti-tumor polysaccharide from Lentinus edodes. Carbohydr. Res. 1976, 47, 99–104. [Google Scholar] [CrossRef]
  27. Chang, C.J.; Lin, C.S.; Lu, C.C.; Martel, J.; Ko, Y.F.; Ojcius, D.M.; Tseng, S.F.; Wu, T.R.; Chen, Y.M.; Young, J.D. Corrigendum: Ganoderma lucidum reduces obesity in mice by modulating the composition of the gut microbiota. Nat. Commun. 2015, 6, 7489. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Li, A.; Shuai, X.; Jia, Z.; Li, H.; Liang, X.; Su, D.; Guo, W. Ganoderma lucidum polysaccharide extract inhibits hepatocellular carcinoma growth by downregulating regulatory T cells accumulation and function by inducing microRNA-125b. J. Transl. Med. 2015, 13, 1–10. [Google Scholar] [CrossRef] [Green Version]
  29. Xu, S.; Dou, Y.; Ye, B.; Wu, Q.; Wang, Y.; Hu, M.; Ma, F.; Rong, X.; Guo, J. Ganoderma lucidum polysaccharides improve insulin sensitivity by regulating inflammatory cytokines and gut microbiota composition in mice. J. Funct. Foods 2017, 38, 545–552. [Google Scholar] [CrossRef]
  30. Chen, X.P.; Yan, C.; Li, S.B.; Chen, Y.G.; Lan, J.Y.; Liu, L.P. Free radical scavenging of Ganoderma lucidum polysaccharides and its effect on antioxidant enzymes and immunity activities in cervical carcinoma rats. Carbohyd. Polym. 2009, 77, 389–393. [Google Scholar]
  31. Liu, Y.; Liu, Z.; Hamada, M.S.; Yin, Y.N.; Ma, Z.H. Characterization of laboratory pyrimethanil-resistant mutants of Aspergillus flavus from groundnut in China. Crop Prot. 2014, 60, 5–8. [Google Scholar] [CrossRef]
  32. Zhang, Z.; Wang, H.; Wang, K.; Jiang, L.; Wang, D. Use of Lentinan To Control Sharp Eyespot of Wheat, and the Mechanism Involved. J. Agric. Food Chem. 2017, 65, 10891–10898. [Google Scholar] [CrossRef]
  33. McDonald, H.; Rovira, A. Development of an Inoculation Technique for Rhizoctonia Solani and Its Application to Screening Cereal Cultivars for Resistance; Parker, C.A., Rovira, A.D., Moore, K.J., Wong, P.T.W., Eds.; Ecology and Management of Soilborne Plant Pathogens, American Phytopathological Society Press: St. Paul, MN, USA, 1985; pp. 174–176. [Google Scholar]
  34. Peng, D.; Li, S.; Chen, C.; Zhou, M. Combined application of Bacillus subtilis NJ-18 with fungicides for control of sharp eyespot of wheat. Biol. Control 2014, 70, 28–34. [Google Scholar] [CrossRef]
  35. Guo, R.; Lin, Z.; Mo, X.; Yang, C. Responses of crop yield and water use efficiency to climate change in the North China Plain. Agric. Water Manag. 2009, 97, 1185–1194. [Google Scholar] [CrossRef]
  36. Hamada, M.S.; Yin, Y.; Chen, H.; Ma, Z. The escalating threat of Rhizoctonia cerealis, the causal agent of sharp eyespot in wheat. Pest Manag. Sci. 2011, 67, 1411–1419. [Google Scholar] [CrossRef]
  37. Wang, Y.; Xu, L.; Li, D.; Teng, M.; Zhang, R.; Zhou, Z.; Zhu, W. Enantioselective bioaccumulation of hexaconazole and its toxic effects in adult zebrafish (Danio rerio). Chemosphere 2015, 138, 798–805. [Google Scholar] [CrossRef] [PubMed]
  38. Baumann, L.; Knörr, S.; Keiter, S.; Nagel, T.; Segner, H.; Braunbeck, T. Prochloraz causes irreversible masculinization of zebrafish (Danio rerio). Environ. Sci. Pollut. Res. 2015, 22, 16417–16422. [Google Scholar] [CrossRef]
  39. Walters, D.R.; Ratsep, J.; Havis, N.D. Controlling crop diseases using induced resistance: Challenges for the future. J. Exp. Bot. 2013, 64, 1263. [Google Scholar] [CrossRef]
  40. Thakur, M.; Sohal, B.S. Role of Elicitors in Inducing Resistance in Plants against Pathogen Infection: A Review. ISRN Biochem. 2013, 2013, 762412. [Google Scholar] [CrossRef] [Green Version]
  41. Aziz, A.; Poinssot, B.; Daire, X.; Adrian, M.; Bézier, A.; Lambert, B.; Joubert, J.M.; Pugin, A. Laminarin elicits defense responses in grapevine and induces protection against Botrytis cinerea and Plasmopara viticola. Mol. Plant-Microbe Interact. 2003, 16, 1118. [Google Scholar] [CrossRef] [Green Version]
  42. Vera, J.; Castro, J.; Gonzalez, A.; Moenne, A. Seaweed Polysaccharides and Derived Oligosaccharides Stimulate Defense Responses and Protection Against Pathogens in Plants. Mar. Drugs 2011, 9, 2514. [Google Scholar] [CrossRef] [PubMed]
  43. Aktar, M.W.; Sengupta, D.; Chowdhury, A. Impact of pesticides use in agriculture: Their benefits and hazards. Interdiscip. Toxicol. 2009, 2, 1–12. [Google Scholar] [CrossRef] [Green Version]
  44. El-Mougy, N.S.; Abd-El-Kareem, F.A.; El-Gamal, N.G.; Fa-Tooh, Y.O. Application of Fungicides Alternatives for Controlling Cowpea Root Rot Disease under Greenhouse and Field Conditions. Egypt J. Phytopathol. 2004, 32, 23–35. [Google Scholar]
  45. Oostendorp, M.; Kunz, W.; Dietrich, B.; Staub, T. Induced disease resistance in plants by chemicals. Eur. J. Plant Pathol. 2001, 107, 19–28. [Google Scholar] [CrossRef]
Figure 1. Three-dimensional chemical structure of the polysaccharides-proteoglycan repeating units-extracted from Ganoderma lucidum. The major polysaccharides identified in the G. lucidum bodies showed to have a backbone of β-(1→3)-linked D-glucopyranosyl residues, with branches of mono-, di- and oligosaccharide side chains substituting at the C-6 of the glucosyl residues in the main chain.
Figure 1. Three-dimensional chemical structure of the polysaccharides-proteoglycan repeating units-extracted from Ganoderma lucidum. The major polysaccharides identified in the G. lucidum bodies showed to have a backbone of β-(1→3)-linked D-glucopyranosyl residues, with branches of mono-, di- and oligosaccharide side chains substituting at the C-6 of the glucosyl residues in the main chain.
Agriculture 12 00055 g001
Figure 2. Flow chart of extracting Ganoderma lucidum polysaccharide.
Figure 2. Flow chart of extracting Ganoderma lucidum polysaccharide.
Agriculture 12 00055 g002
Figure 3. Effect of seed treated GLP on transcript quantity of wheat (Jimai 22) disease resistance-related gene. GLP 4: 4% GLP, GLP 8: 8% GLP. * indicates significant difference at 0.05 level.
Figure 3. Effect of seed treated GLP on transcript quantity of wheat (Jimai 22) disease resistance-related gene. GLP 4: 4% GLP, GLP 8: 8% GLP. * indicates significant difference at 0.05 level.
Agriculture 12 00055 g003
Figure 4. Effect of seed treated GLP on the transcript quantity of the maize (Zhengdan 958) disease resistance-related gene. GLP 15: 15% GLP, GLP 30: 30% GLP. * indicates significant difference at 0.05 level.
Figure 4. Effect of seed treated GLP on the transcript quantity of the maize (Zhengdan 958) disease resistance-related gene. GLP 15: 15% GLP, GLP 30: 30% GLP. * indicates significant difference at 0.05 level.
Agriculture 12 00055 g004
Table 1. Groups of real-time quantitative PCR (RT-qPCR) primers used to amplify genes pecific regions.
Table 1. Groups of real-time quantitative PCR (RT-qPCR) primers used to amplify genes pecific regions.
Accession No.GenesLeft Primer 5′-3′Right Primer 5′-3′
MaizeGRMZM2G103342PODAGTAGATGATCCCTGTCCGCGCCGCCACCCTCTTATTAGA
GRMZM2G112488PR-10TGAAGGTGGACTCGACGTACCGATCGCATGCATGGTCTAC
GRMZM2G127087TPSGACCAGACAAGAGCTACCGACCCATTCCAACAAACGCAGA
GRMZM2G402613PR-5CGGCAACAGCAACTACCAAGGCACACAAATCCAGCTACGT
GRMZM2G453805CHCTcCGTGCAGAACAACTACAGCAATGCGTCTTTGTCTCCCGAT
GRMZM2G162505CHITACCTCCACCAATCCAACCAACAACAGCCGCTACAAGTACC
GRMZM2G336824OMTCCACCCTTCTCCAGATCCTCAGACTCACAAAGGGAGCCAA
AC205502.4_FG004TPS21AGAGGTCACACGCTTCATGAGCCATGCTCACTGATGTAGC
GRMZM2G148904EACACGTACCCCATCTTCCTCAGATCATCAATCGTCGGAGCG
GRMZM2G028306TPCAGAGAAAAGGCTGGAGTGCTGATTTAGTCGCTGCAGGGTG
GRMZM2G136372PR5CTCCAGCCAACTTCTTTCTTTGGGGGTGAACATCATCGTCTTAT
GRMZM2G449681WRKY53GACATTGTGGTCCCATCTGATGAGAGGGGGAGAGAAGAGAT
GRMZM2G079112JA-COL1TGGAACCCCTAAAAATTTCCCTGATCTGTTTCCCTCCTCGAC
GRMZM2G091276JAR1TCCTCTCTATTGCGAAAAGGTTAGTGCCAGTAAGAAAGTTCAGA
GRMZM2G001930JA-MYC2AATCCGCATTCTGAACCATTTCGAAAGAGGAGGAGAAATGGTGG
U76259EF1AGCCTGGTATGGTTGTTACTCATACCCACGCTTCAGATCC
WheatAK455337.1IR5GCCGTTCGCATAGTCAATCCGCACCATTATTCGCTTGT
AK332579.1IR2GACATCCATTTCCAGGGGCGCGGTCTGGGCATTCATC
JF718349.1DQ-GLUGCTGGAAAGGATGTTGCTTGCCCGTTACACTTGGAT
HG670306.1IR6CACTGGGTCGTGACACTTCTCCTCCTCTTCCTTGTATGCTG
HG670306.1WMC44GGTCTTCTGGGCTTTGATCCTGTGTTGCTAGGGACCCGTAGTGG
AK446945.1csGSAAGATTGTTCACAGATCCATGTCAGAGTATTCCGGCTCAAAAAGG
AK448410.1WMS533AAGGCGAATCAAACGGAATAGTTGCTTTAGGGGAAAAGCC
XM_016633336.1NbPR1aCGTTGAGATGTGGGTCAATGCCTAGCACATCCAACACGAA
AK449901.1NbrbohBGTGATGCTCGTTCTGCTCTTCTTTAGCCTCAGGGTGGTTG
XM_013385118.1Xgwm526CAATAGTTCTGTGAGAGCTGCGCCAACCCAAATACACATTCTCA
AK449144.1Xwmc364ATCACAATGCTGGCCCTAAAACCAGTGCCAAAATGTCGAAAGTC
HG670306.1RS33TGGAGAGGACAGCCCATGGAGTTGGTAGTAGGTGCGCCCTTGCTCACCATGCTGCTGATAACATGATCCA
AK450528.1ActinCACTGGAATGGTCAAGGCTGCTCCATGTCATCCCAGTTG
Table 2. In vivo assays test of GLP and fungicides on Fusarium graminearum.
Table 2. In vivo assays test of GLP and fungicides on Fusarium graminearum.
TreatmentsRegression EquationR2EC50 Value
(mg·L−1)
95%Confidence Interval
(mg·L−1)
ProchlorazY = 5.794 + 0.750 X0.9740.0880.072~0.106
FludioxonilY = 5.170 + 0.750 X0.9620.5930.442~0.795
HexaconazoleY = 5.095 + 0.814 X0.9800.7640.594~0.981
MetalaxylY = 3.102 + 1.014 X0.9605.9274.419~7.650
FluopimomideY = 5.195 + 1.045 X0.9696.1375.643~6.983
GLP////
Note: GLP has no inhibitory effect on Fusarium graminearum.
Table 3. In vivo assays test of GLP and fungicides on Drechslera sorokiniana.
Table 3. In vivo assays test of GLP and fungicides on Drechslera sorokiniana.
TreatmentsRegression EquationR2EC50 Value
(mg·L−1)
95%Confidence Interval
(mg·L−1)
HexaconazoleY = 1.29 + 1.54 X0.9880.1440.111~0.176
ProchlorazY = 1.06 + 1.40 X0.9830.1820.125~0.229
FludioxonilY = 0.28 + 1.98 X0.9810.7660.624~0.908
DifenoconazoleY = 0.92 + 1.57 X0.9683.2592.635~3.913
ThiramY = −1.74 + 2.51 X0.9736.9155.526~8.314
FluopimomideY = −5.28 + 3.22 X0.98543.3338.21~48.45
GLP////
Note: GLP has no inhibitory effect on Drechslera sorokiniana.
Table 4. In vivo assays test of GLP and fungicides on Rhizoctonia cerealis.
Table 4. In vivo assays test of GLP and fungicides on Rhizoctonia cerealis.
TreatmentsRegression EquationR2EC50 Value
(mg·L−1)
95%Confidence Interval
(mg·L−1)
HexaconazoleY = 2.79 + 2.30 X0.9520.0940.032~1.255
FludioxonilY = 0.76 + 1.47 X0.9850.3120.081~0.574
FluopimomideY = −1.00 + 1.62 X0.9864.1693.125~4.852
ProchlorazY = −1.17 + 1.54 X0.9835.7385.112~6.312
GLP////
Note: GLP has no inhibitory effect on Rhizoctonia cerealis.
Table 5. Effects of seed dressing on wheat germination.
Table 5. Effects of seed dressing on wheat germination.
Wheat Cultivated VarietyTreatmentDosage
(mL/100 kg Seed)
Germination Rate (%)
Control Germination 50%Control Total Germination3 Days after Control Total Germination
Jimai 22CK10050.00 b95.00 bc97.00 b
4% GLP10052.25 a97.25 a98.25 a
8% GLP10053.25 a96.25 ab97.25 ab
0.5% Hexaconazole10050.00 b95.00 bc95.75 c
1% Hexaconazole10046.75 c94.00 c95.75 c
2% Hexaconazole10044.75 d91.75 d95.50 c
0.5% H + 4% GLP10050.25 b96.75 ab97.00 b
Shannong 23CK10048.75 b96.00 b97.00 b
4% GLP10050.00 ab96.75 ab97.75 ab
8% GLP10051.75 a98.25 a98.25 a
0.5% Hexaconazole10048.75 b95.00 b95.75 c
1% Hexaconazole10047.25 b92.75 c95.75 c
2% Hexaconazole10044.00 c90.50 d96.75 bc
0.5% H + 4% GLP10049.00 b95.00 b97.00 b
Luyuan 502CK10048.00 b95.00 bc96.50 ab
4% GLP10048.25 b96.25 ab97.00 a
8% GLP10049.25 ab97.25 a97.25 a
0.5% Hexaconazole10050.25 a96.00 ab96.00 b
1% Hexaconazole10045.75 c94.25 c96.00 b
2% Hexaconazole10042.75 d91.75 d94.75 c
0.5% H + 4% GLP10048.00 b96.00 ab96.00 b
Note: CK means that seeds are treated with sterile water. 0.5% H + 4% GLP stands for the combination of hexaconazole with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests. Table 6, Table 7, Table 8, Table 9, Table 10, Table 11, Table 12, Table 13 and Table 14 are the same.
Table 6. Effects of seed dressing on maize germination.
Table 6. Effects of seed dressing on maize germination.
Maize Cultivated VarietyTreatmentDosage
(mL/100 kg Seed)
Germination Rate (%)
Control Germination 50%Control Total Germination3 Days after Control Total Germination
Zhengdan 958CK10049.00 b96.75 a97.50 b
15% GLP10051.25 a97.00 a97.75 b
30% GLP10051.75 a97.25 a99.25 a
20% Prochloraz10049.00 b96.75 a97.75 b
40% Prochloraz10047.75 c95.75 b98.00 b
80% Prochloraz10047.25 c94.50 c99.25 a
20% P + 15% GLP10049.75 b97.00 a97.75 b
Xianyu 335CK10049.00 b95.75 c98.75 a
15% GLP10052.25 a97.00 b97.75 b
30% GLP10053.75 a98.25 a99.00 a
20% Prochloraz10048.00 b97.00 b97.75 b
40% Prochloraz10046.00 c95.75 c97.50 b
80% Prochloraz10045.25 c94.50 d97.50 b
20% P + 15% GLP10049.00 b96.75 b99.00 a
Luning 202CK10049.00 b96.75 b98.75 a
15% GLP10050.25 ab96.75 b99.00 a
30% GLP10051.25 a98.25 a99.25 a
20% Prochloraz10048.75 b98.00 a99.00 a
40% Prochloraz10046.50 c94.50 d97.75 b
80% Prochloraz10046.00 c95.75 c97.50 b
20% P + 15% GLP10048.75 b97.75 a99.00 a
Note: 20% P + 15% GLP stands for the combination of prochloraz with GLP. Different lower-cases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 7. Effects of seed dressing on the growth of wheat seedlings.
Table 7. Effects of seed dressing on the growth of wheat seedlings.
Wheat Cultivated VarietyTreatmentDosage
(mL/ 100 kg Seed)
Height (cm)
7 d14 d21 d
Jimai 22CK1007.35 c18.50 b27.50 b
4% GLP1009.03 b20.56 a28.02 b
8% GLP1009.81 a21.18 a30.96 a
0.5% Hexaconazole1007.18 c18.95 b26.96 c
1% Hexaconazole1006.25 d15.94 c26.35 c
2% Hexaconazole1005.28 e15.29 c26.02 c
0.5% H + 4% GLP1007.22 c18.75 b28.55 b
Shannong 23CK1006.28 c15.50 b26.50 b
4% GLP1007.50 b16.80 a27.00 b
8% GLP1008.75 a18.06 a28.50 a
0.5% Hexaconazole1006.39 c15.0 bc26.96 b
1% Hexaconazole1005.47 d14.33 c26.03 c
2% Hexaconazole1004.84 d13.91 c25.78 c
0.5% H + 4% GLP1006.52 c15.85 b27.12 b
Luyuan 502CK1007.01 d17.50 c26.50 b
4% GLP1009.84 b20.75 b28.22 a
8% GLP10011.96 a24.33 a27.85 a
0.5% Hexaconazole1006.50 e16.96 c26.35 b
1% Hexaconazole1006.06 e16.34 d25.96 b
2% Hexaconazole1005.43 e16.02 d25.78 b
0.5% H + 4% GLP1007.44 d17.69 c26.86 b
Note: Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 8. Effects of seed dressing on the growth of maize seedlings.
Table 8. Effects of seed dressing on the growth of maize seedlings.
Maize Cultivated VarietyTreatmentDosage
(mL/100 kg Seed)
Height (cm)
7 d14 d21 d
Zhengdan 958CK1007.23 c28.50 b55.50 a
15% GLP1007.88 b30.56 a58.22 a
30% GLP1008.31 a31.18 a58.56 a
20% Prochloraz1007.18 c28.31 b56.39 a
40% Prochloraz1007.06 c28.25 b55.29 a
80% Prochloraz1006.89 c27.96 b55.18 a
20% P + 15% GLP1007.83 b30.47 b55.49 a
Xianyu 335CK1006.52 c26.50 b55.50 b
15% GLP1007.50 b27.00 b56.78 b
30% GLP1008.57 a28.50 a58.06 a
20% Prochloraz1006.48 c27.12 b56.23 b
40% Prochloraz1006.29 c26.51 b55.85 b
80% Prochloraz1006.37 c26.02 b54.95 b
20% P + 15% GLP1007.35 b26.94 b56.17 b
Luning 202CK1005.36 b24.50 c47.50 a
15% GLP1006.48 a25.22 b47.75 a
30% GLP1006.96 a25.85 b48.33 a
20% Prochloraz1005.22 b24.35 c47.88 a
40% Prochloraz1005.08 b24.12 c46.89 a
80% Prochloraz1005.11 b23.98 c46.85 a
20% P + 15% GLP1006.44 a25.29 c47.69 a
Note: 20% P + 15% GLP stands for the combination of prochloraz with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 9. Control effect of the seed treatment on wheat sharp eyespot.
Table 9. Control effect of the seed treatment on wheat sharp eyespot.
Wheat Cultivated VarietyAgentiaDosage
(mL/100 kg Seed)
Control Effect (%)
7 d14 d21 d
Jimai 224% GLP10028.1 ± 1.7 d24.5 ± 2.1 d22.9 ± 1.9 d
8% GLP10032.7 ± 2.6 b31.4 ± 2.4 b29.6 ± 3.7 c
0.5% Hexaconazole10050.3 ± 4.9 c43.7 ± 1.8 c40.1 ± 2.5 b
1% Hexaconazole10079.7 ± 7.4 a69.8 ± 7.1 a64.3 ± 3.7 a
0.5% H + 4% GLP10075.8 ± 2.7 a68.1 ± 1.9 a66.6 ± 2.4 a
Shannong 234% GLP10024.5 ± 0.6 d21.9 ± 0.4 e19.6 ± 1.1 d
8% GLP10030.8 ± 1.5 bc27.9 ± 1.3 d26.2 ± 3.7 c
0.5% Hexaconazole10043.4 ± 3.2 c38.6 ± 1.6 c30.8 ± 2.2 c
1% Hexaconazole10072.0 ± 4.3 a66.5 ± 3.9 a59.4 ± 2.5 b
0.5% H + 4% GLP10067.1 ± 5.3 b65.7 ± 1.3 a65.2 ± 2.8 a
Luyuan 5024% GLP10030.5 ± 1.8 d27.9 ± 2.7 d26.0 ± 1.6 d
8% GLP10036.0 ± 3.1 c32.4 ± 1.3 c29.6 ± 0.8 c
0.5% Hexaconazole10051.6 ± 3.7 b47.7 ± 2.5 b42.2 ± 1.2 b
1% Hexaconazole10077.3 ± 8.3 a71.5 ± 2.9 a63.6 ± 2.0 a
0.5% H + 4% GLP10073.4 ± 4.1 a68.7 ± 2.6 a65.2 ± 1.2 a
Note: 0.5% H + 4% GLP stands for the combination of hexaconazole with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 10. Control effect of seed treatment on wheat root rot.
Table 10. Control effect of seed treatment on wheat root rot.
Wheat Cultivated VarietyAgentiaDosage
(g a.i./100 kg Seed)
Control Effect (%)
7 d14 d21 d
Jimai 224% GLP10029.8 ± 1.9 d26.3 ± 2.7 d24.5 ± 1.7 c
8% GLP10035.4 ± 3.1 c32.7 ± 2.2 c30.8 ± 1.7 b
0.5% Hexaconazole10046.9 ± 4.5 b40.3 ± 2.9 b35.7 ± 3.5 b
1% Hexaconazole10076.3 ± 3.4 a62.4 ± 4.6 a55.3 ± 4.1 a
0.5% H + 4% GLP10079.4 ± 3.6 a70.3 ± 4.1 a61.5 ± 3.4 a
Shannong 234% GLP10028.2 ± 1.7 d25.7 ± 1.6 d22.9 ± 1.8 d
8% GLP10038.5 ± 2.1 c34.7 ± 1.9 c30.5 ± 1.6 c
0.5% Hexaconazole10052.4 ± 2.8 b46.8 ± 3.1 b42.5 ± 1.7 b
1% Hexaconazole10080.2 ± 7.9 a74.5 ± 9.1 a68.6 ± 5.7 a
0.5% H + 4% GLP10082.6 ± 3.8 a76.7 ± 4.2 a74.9 ± 2.5 a
Luyuan 5024% GLP10030.5 ± 2.6 d29.3 ± 1.8 c28.6 ± 2.4 c
8% GLP10039.3 ± 2.8 c35.4 ± 2.3 b34.7 ± 3.1 b
0.5% Hexaconazole10049.2 ± 2.6 b41.5 ± 2.5 b37.8 ± 3.5 b
1% Hexaconazole10080.4 ± 3.5 a71.5 ± 3.5 a65.4 ± 2.5 a
0.5% H + 4% GLP10081.5 ± 4.2 a73.6 ± 3.2 a67.1 ± 2.9 a
Note: 0.5% H + 4% GLP stands for the combination of hexaconazole with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 11. Control effect of seed treatment on maize stalk rot.
Table 11. Control effect of seed treatment on maize stalk rot.
Maize Cultivated VarietyAgentiaDosage
(g a.i./100 kg Seed)
Control Effect (%)
7 d14 d21 d
Zhengdan 95815% GLP10029.5 ± 3.6 d27.8 ± 2.1 d26.2 ± 2.4 d
30% GLP10037.6 ± 1.9 c34.8 ± 1.9 c32.2 ± 2.3 c
20% Prochloraz10068.8 ± 3.5 b55.6 ± 3.4 b49.3 ± 5.6 b
40% Prochloraz10088.8 ± 7.8 a75.9 ± 6.9 a60.6 ± 7.8 a
20% P + 15% GLP10084.2 ± 7.7 a75.6 ± 2.4 a67.9 ± 4.1 a
Xianyu 33515% GLP10030.2 ± 1.8 d26.5 ± 1.7 d23.2 ± 1.7 d
30% GLP10039.7 ± 2.4 c37.6 ± 1.2 c34.9 ± 2.6 c
20% Prochloraz10068.2 ± 3.7 b53.1 ± 4.2 b46.2 ± 3.1 b
40% Prochloraz10082.9 ± 3.7 a74.4 ± 2.7 a65.2 ± 3.7 a
20% P + 15% GLP10080.8 ± 3.9 a73.8 ± 6.7 a65.1 ± 3.4 a
Luning 20615% GLP10027.3 ± 2.5 d23.2 ± 2.1 c21.6 ± 2.3 c
30% GLP10038.8 ± 2.3 c36.4 ± 1.7 b35.1 ± 1.2 b
20% Prochloraz10053.5 ± 3.8 b37.6 ± 3.6 b32.9 ± 3.7 b
40% Prochloraz10076.2 ± 2.1 a62.5 ± 3.7 a56.2 ± 4.5 a
20% P + 15% GLP10073.7 ± 3.5 a70.7 ± 2.6 a61.9 ± 3.4 a
Note: 20% P + 15% GLP stands for the combination of prochloraz with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 12. Field control effect of seed treated on wheat sharp eyespot and wheat root rot.
Table 12. Field control effect of seed treated on wheat sharp eyespot and wheat root rot.
YearWheat Cultivated VarietyAgentia Treatment
(100 mL/100 kg Seed)
Wheat Sharp EyespotWheat Root Rot
Before OverwinteringJointing StageFilling Period
2017–2018Jimai 22CK///
8% GLP38.6 ± 1.7 b28.4 ± 1.9 c21.3 ± 0.6 d36.2 ± 2.2 b
1% Hexaconazole80.6 ± 2.3 a58.4 ± 2.1 b38.6 ± 2.4 b81.3 ± 4.9 a
0.5% H + 4% GLP78.7 ± 2.5 a68.2 ± 4.2 a42.4 ± 4.5 a75.9 ± 3.7 a
Shannong 23CK///c
8% GLP35.7 ± 1.5 b26.9 ± 1.1 d19.8 ± 1.7 d32.8 ± 11.9 b
1% Hexaconazole81.3 ± 2.5 a62.4 ± 3.2 b39.2 ± 2.6 b79.6 ± 3.8 a
0.5% H + 4% GLP78.8 ± 2.4 a67.3 ± 2.7 a42.8 ± 2.8 a75.3 ± 4.1 a
Luyuan 502CK///
8% GLP32.7 ± 1.2 b29.3 ± 1.5 c20.9 ± 1.2 d36.4 ± 3.3 b
1% Hexaconazole80.5 ± 5.7 a63.2 ± 4.4 b30.3 ± 1.8 b70.6 ± 2.9 a
0.5% H + 4% GLP79.6 ± 5.2 a70.4 ± 1.9 a41.9 ± 2.3 a73.3 ± 3.1 a
2018–2019Jimai 22CK///
8% GLP36.3 ± 1.6 b26.2 ± 1.4 d20.8 ± 1.7 d40.2 ± 1.1 b
1% Hexaconazole76.9 ± 2.5 a56.3 ± 2.1 b35.6 ± 2.3 b85.8 ± 7.6 a
0.5% H + 4% GLP75.8 ± 2.8 a63.3 ± 2.9 a41.7 ± 3.2 a80.5 ± 5.2 a
Shannong 23CK///c
8% GLP37.9 ± 0.4 b32.2 ± 1.7 d24.2 ± 0.9 b30.4 ± 2.4 b
1% Hexaconazole80.3 ± 4.1 a64.5 ± 3.5 b40.2 ± 3.3 a79.2 ± 6.6 a
0.5% H + 4% GLP78.9 ± 7.2 a69.2 ± 4.9 a43.7 ± 1.7 a72.4 ± 3.3 a
Luyuan 502CK///
8% GLP35.6 ± 2.1 b30.2 ± 1.4 c22.7 ± 1.7 c34.2 ± 2.9 b
1% Hexaconazole81.4 ± 3.8 a61.2 ± 2.2 b29.8 ± 1.9 b75.8 ± 4.1 a
0.5% H + 4% GLP77.1 ± 5.1 a72.7 ± 3.6 a40.6 ± 1.2 a70.6 ± 5.2 a
Note: 0.5% H + 4% GLP stands for the combination of hexaconazole with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 13. Field control effect of seed treatment on maize stalk rot.
Table 13. Field control effect of seed treatment on maize stalk rot.
YearMaize Cultivated
Variey
AgentiaDosage
(mL/100 kg Seed)
Control Effect (%)
30 July20 August
2017Zhengdan 95830% GLP10032.5 ± 2.5 b24.7 ± 1.9 b
40% Prochloraz10076.4 ± 5.2 a59.8 ± 4.3 a
20% P + 15%GLP10073.2 ± 4.1 a56.2 ± 5.7 a
Xianyu 33530% GLP10033.9 ± 2.6 b25.7 ± 2.4 b
40% Prochloraz10075.5 ± 1.9 a57.2 ± 4.3 a
20% P + 15% GLP10076.4 ± 2.8 a60.1 ± 5.3 a
Luning 20630% GLP10035.9 ± 1.9 b34.2 ± 1.4 b
40% Prochloraz10075.3 ± 3.5 a54.4 ± 2.8 a
20% P + 15% GLP10074.1 ± 2.7 a52.5 ± 1.6 a
2018Zhengdan 95830% GLP10038.2 ± 1.5 b29.7 ± 2.1 b
40% Prochloraz10071.6 ± 4.6 a55.3 ± 3.1 a
20% P + 15% GLP10079.5 ± 6.2 a61.4 ± 2.8 a
Xianyu 33530% GLP10036.5 ± 2.9 b24.7 ± 1.4 b
40% Prochloraz10080.6 ± 7.3 a60.5 ± 5.2 a
20% P + 15% GLP10073.3 ± 4.8 a53.2 ± 2.9 a
Luning 20630% GLP10036.1 ± 1.7 b25.4 ± 0.6 b
40% Prochloraz10078.2 ± 4.8 a56.3 ± 2.2 a
20% P + 15% GLP10082.6 ± 2.2 a50.8 ± 2.7 a
Note: 20% P + 15% GLP stands for the combination of prochloraz with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Table 14. Effects of chemical seed treatment on the yield of wheat and maize.
Table 14. Effects of chemical seed treatment on the yield of wheat and maize.
Cultivated VarietyTreatmentDosage
(mL/100 kg Seed)
Yield (kg·hm−2)
20172018
MaizeZhengdan 958CK1008233.80 b8193.75 c
30% GLP1008344.05 ab8252.10 bc
40% Prochloraz1008555.70 a8584.35 a
20%P + 15% GLP1008582.85 a8526.45 ab
Xianyu 335CK1008252.25 b8440.95 b
30% GLP1008406.45 ab8549.10 b
40% Prochloraz1008631.30 a8849.10 a
20%P + 15% GLP1008624.25 a8890.20 a
Luning 202CK1007596.60 b7865.55 b
30% GLP1007652.70 ab8125.80 ab
40% Prochloraz1007931.25 a8503.80 a
20%P + 15% GLP1007953.90 a8577.90 a
WheatJimai 22CK1007248.60 b6253.95 b
8% GLP1007344.45 ab6604.80 ab
1% Hexaconazole1007554.25 ab6454.05 b
0.5% H + 4% GLP1007692.84 a7128.60 a
Shannong 23CK1007362.45 b6224.40 b
8% GLP1007492.05 ab6610.20 ab
1% Hexaconazole1007624.35 ab6440.55 ab
0.5% H + 4% GLP1007910.40 a6979.35 a
Luyuan 502CK1007210.95 b5950.95 b
8% GLP1007338.75 ab6318.75 ab
1% Hexaconazole1007522.05 ab6277.90 ab
0.5% H + 4% GLP1007722.90 a6535.20 a
Note: 0.5% H + 4% GLP stands for the combination of hexaconazole with GLP. Different lowercases in the same column indicate significantly different at p < 0.05 level according to Duncan’s multiple range tests.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Yang, X.; Sun, S.; Chen, Q.; Zhang, Z.; Wang, J.; Liu, Y.; Wang, H. A Polysaccharide of Ganoderma lucidum Enhances Antifungal Activity of Chemical Fungicides against Soil-Borne Diseases of Wheat and Maize by Induced Resistance. Agriculture 2022, 12, 55. https://doi.org/10.3390/agriculture12010055

AMA Style

Yang X, Sun S, Chen Q, Zhang Z, Wang J, Liu Y, Wang H. A Polysaccharide of Ganoderma lucidum Enhances Antifungal Activity of Chemical Fungicides against Soil-Borne Diseases of Wheat and Maize by Induced Resistance. Agriculture. 2022; 12(1):55. https://doi.org/10.3390/agriculture12010055

Chicago/Turabian Style

Yang, Xiu, Shoumin Sun, Qiqi Chen, Zhongxiao Zhang, Jie Wang, Yali Liu, and Hongyan Wang. 2022. "A Polysaccharide of Ganoderma lucidum Enhances Antifungal Activity of Chemical Fungicides against Soil-Borne Diseases of Wheat and Maize by Induced Resistance" Agriculture 12, no. 1: 55. https://doi.org/10.3390/agriculture12010055

APA Style

Yang, X., Sun, S., Chen, Q., Zhang, Z., Wang, J., Liu, Y., & Wang, H. (2022). A Polysaccharide of Ganoderma lucidum Enhances Antifungal Activity of Chemical Fungicides against Soil-Borne Diseases of Wheat and Maize by Induced Resistance. Agriculture, 12(1), 55. https://doi.org/10.3390/agriculture12010055

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop