A case study of non-traditional treatments for the control of wheat stem rust disease

Abstract

Wheat stem rust causes by Puccinia graminis f. sp. tritici is a serious threat to wheat production all over the world. This study evaluated the efficacy of Bacillus subtilis, B. polymyxa and B. megaterium, Eugenol and leaf extract of Artemisia cina against the disease, and the involved mechanisms in disease resistance. B. subtilis and Eugenol treatments inhibited spore germination and increased incubation and latent periods than other treatments. Additionally, the lowest infection type, pustule length and pustule width, and receptivity (no. of pustules) were recorded in case of B. subtilis and Eugenol treatments compared with the check control. The best results in disease assessment were achieved by foliar spray application 24 h before and after inoculation. Abnormalities, lysis, collapse, and shrinking of urediniospores were recorded in treated leaves. The activities of antioxidant defense enzymes, i.e., catalase (CAT), peroxidase (POX), and polyphenoloxidase (PPO), were significantly increased in B. subtilis and Eugenol treatments. On the other hand, electrolyte leakage was decreased. The active compounds in B. subtilis were revealed by utilizing GC-MS analysis.

Background

In Egypt, wheat is liable to attack by many diseases such as rusts, powdery mildew, and smut. Wheat rusts are still the main biotic stress, which affect the yield quantity and quality of most wheat cultivars under Egyptian conditions (Omara and Abdelaal 2018). Stem rust, caused by Puccinia graminis f. sp. tritici, is one of the 3 main rusts attacking wheat plants in Egypt. Disease severity increases in the absence of resistance varieties, and the disease outbreak may occur suddenly, particularly with the continuous genetic changes of host pathogen interactions (Omara et al. 2017).

The main strategy for stem rust management depends on planting resistant varieties, early detection of the disease, and successful application of effective fungicides at the right time with sufficient doses. Although several fungicides are effective for disease control, but they may have a negative impact on human health and safety due to the persistence of residues and exposure risks (Hermas et al. 2008). The intensive repeated application of fungicides causes environmental pollution and leads to the development of new pathogen strains, which could be more aggressive if they have resistance against the routinely used fungicides (Abd El-Moneim et al. 2011). It was reported that the application of biological control treatments, such as Bacillus subtilis, B. polymyxa, B. circilance, Pseudomonas fluorescens, and Trichoderma harzianum, and some chemical inducers such as Eugenol, Allicin, and Fulvic acid were effective in management strategies against different pathogens (El-Sawy et al. 2016 and Omara et al. 2019), particularly against P. graminis (Abd El-Moneim et al. 2011). Several Bacillus spp. are antagonistic to plant pathogenic fungi due to the production of at least 66 different antibiotic compounds (Ferreira et al. 1991). Eugenol is an active ingredient that was used successfully in the elimination of many plant pathogens. Eugenol treatment reduced rust severity (%) and AUDPC at adult stage by inhibition of P. striiformis urediniospores germination, reduction of incubation and latent periods at the seedling stage (El-Sawy et al. 2016). Similarly, the application of Artemisia cina was effective in the control of wheat leaf rust disease through increased incubation and latent periods and prevention of urediniospores germination. Therefore, successful and safe approaches in plant protection, using biological and natural inducers, are required (Omara et al. 2015 and 2019).

Plant infection with different pathogens is related with the accumulation of reactive oxygen species (ROS). So, antioxidant defense system seems to be a common response to oxidative stress (Omara and Abdelaal 2018). After pathogen attack, several antioxidant enzymes such as peroxidase, polyphenol oxidase, and catalase start its function by decreasing ROS levels and elimination of detrimental effects under disease stress (Hafez et al. 2014). Also, electrolyte leakage (EL) is an indication of increased permeability of the plasma membrane under disease stress (Omara et al. 2015).

Therefore, the aim of this investigation was to evaluate the effect of foliar application of non-traditional treatments against the wheat stem rust pathogen as well as understanding the physiological and biochemical changes in the treated wheat plants under stress of P. graminis f. sp. tritici.

Materials and methods

Bacterial strains

Bacillus subtilis, B. polymyxa, and B. megaterium used in this study were kindly obtained from Agric. Microbiology Department, Soils, Water and Environmental Res. Inst. (SWERI), Agricultural Research Center (ARC), Giza, Egypt. The strains were maintained on nutrient agar medium for 48 h at 28 ± 2 °C and stored in refrigerator at 4 °C until use after Difco Manual (1985).

Preparation of bacterial suspension

Bacterial suspension was prepared by cultivating Bacillus strains on nutrient broth medium using shaking flask submerged culture. Conical flasks (500 ml) containing 200 ml of the respective media were inoculated with 1 ml bacterial inocula of 24 h old culture and incubated in rotary shaking incubator (120 rpm) at 28 ± 2 °C for 72 h. The bacterial suspension density was adjusted to 10⁶ cfu/ml (Sun et al. 2013). The obtained cell suspensions were foliar sprayed directly on the wheat plants (100 ml for each treatment). Foliar spraying of wheat plants was applied using the 2 applications methods, i.e., 24 h before inoculation and 24 h before and after inoculation.

Natural materials

1. Eugenol

Eugenol was kindly supplied by the Faculty of Pharmacy, Ain Shams University, Egypt, in the form of crude powder and used at concentration of 0.5 g/l.

2. Artemisia cina extract

Artemisia cina leaves were air-dried for 72 h at 35 °C then ground by a blender into fine powder. One hundred grams of the powder was macerated in 500 ml of ethanol and acetone mixture (at the ratio of 1:1, v/v) by shaking for 5 h on an electrical shaker. Extract was filtered through sterilized filter papers and then dried over anhydrous sodium sulfate and evaporated to dryness. The residue was dissolved in ethanol 99% (Lopa, India) to reach the desired concentrations (2%) as described by Morsy (2010).

Microscope examination

Effect of treatments on urediniospores germination and disease symptoms

Under in vitro conditions, fresh urediniospores were sprayed on cleaned and sterilized glass slides (Nair and Ellingboe 1962). Slides were covered with a thin smear of 2% water agar then amended with different treatments. Slides were placed on V-shaped glass rods in sterilized petri-dishes with moistened filter papers. Slides were incubated at 25 °C for 12 h under full light condition and microscopically examined at × 40 magnification to determine the percentage of spore-germination (Reifschneider et al. 1985). Spores were considered to have germinated if a germ tube, as long as the width, was produced (Menzies and Belanger 1996). Percentages of germination were calculated for 100 spores on a slide. Three slides were examined for each treatment. Slides with water agar free from any treatment were used as control.

Meanwhile under greenhouse conditions, after symptoms appearance, the treated plants with the previous treatments and the check treatment were sampled at the 4th day, and specimens of lesions were prepared for microscopic examination. Leaves showing stem rust pustules were maintained in lactophenol on slides. Abnormality or deleterious effects on P. graminis were observed using light microscope and photographed.

Greenhouse experiments

Incubation, latent periods, pustule size, and receptivity (number of pustules)

Seeds of Gemmeiza-11 cultivar (5–7 grains) were sown in 10 cm plastic pots filled with clay soil (400 g). After 7 days from planting (seedling stage), the plants were inoculated with urediniospores (TTSPQ race) of stem rust. Seedling reaction was recorded as resistance (R) or susceptible (S) depending on the produced infection types. The infection types, 0, 0;, 1, and 2, are considered to be resistant (R) or low infection type (L), while 3 and 4 are considered to be susceptible (S) or high infection type (H) according to the scale adopted by Stakman et al. (1962) as shown in Table 1. After inoculation, the plants were treated with cell suspensions of Bacillus subtilis, B. polymyxa and B. megaterium, Eugenol, and A. cina extract at 24 h before inoculation and 24 h before and after inoculation.

Table 1 Wheat stem rust infection types used in disease assessment for seedling stage

Incubation period (IP) (the number of days between inoculations to the commencement of the first pustule) was recorded. Latent period (LP) was calculated as described by Parlevliet (1975) by totaling the number of observed pustules on marked leaves every day until no more appearance of pustules. Additionally, the time between inoculation and the appearance of 50% of the pustules were recorded. In order to compare pustules size on the first leaf of susceptible plants, the length and width dimensions of 20 pustules were estimated. The method explained by Parlevliet and Kuiper (1977) was used to calculate the number of pustules per square centimeter per unit leaf area (2.0 × 0.5 cm²) on the upper side of the leaves.

Laboratories studies

Enzyme activities and electrolyte leakage

The activities of antioxidant defense enzymes including catalase (CAT), peroxidase (POX), and polyphenoloxidase (PPO) were assayed in wheat treated leaves with B. subtilis, B. polymxa, B. megaterium, A. cinia, and Eugenol at 24, 72, and 168 h after inoculation. Fresh leaves (0.5 g) were homogenized at 4 °C and centrifuged (12.000 rpm, 20 min, 4 °C). The total soluble enzyme activities were estimated spectrophotometrically in the supernatant. PPO activity was determined according to the methods described by Malik and Singh (1980). POX activity was measured according to the procedure suggested by Hammerschmidt et al. (1982). CAT activity was measured according to Aebi (1984). Additionally, the percentage of electrolyte leakage was recorded as initial conductivity/final conductivity × 100 M according to Szalai et al. (1996).

GC-MS analysis

The method of hydrolysis-methanolysis was used to obtain the methyl esters without dehydration of the ß-hydroxy fatty acids and to avoid the formation of the mixture of α- and ß-monounsaturated fatty acids (Aveldano and Horrocks 1983). Volatile compounds in the extracts were analyzed by gas chromatography and mass spectrometry. Extract solutions (0.2%) in methanol were injected into a HP 6890N gas chromatograph equipped with HP 5975 mass detector and fused silica capillary column HP5 MS (5% phenyl methyl silicone, 30 m length, 0.25 mm i.d.). The temperature was programmed from 30 (1 min) to 230 °C (20 min) at the rate of 4 °C/min. Detector was heated at 250 °C, injector at 230 °C. Helium was used as a carrier gas at 5-psi pressure. Mass spectra were obtained by electron ionization at 70 eV.

Statistical analysis

Data were statistically analyzed by analysis of variance, using software package SPSS 22. A randomized complete block design (RCBD) with 4 replicates (five pots per replicate) was used. Principle components analysis (PCA) of incubation and latent periods, infection type, pustule length, pustule width, receptivity (no. of pustule), catalase (CAT), peroxidase (POX), polyphenoloxidase (PPO), and electrolyte leakage was performed, using statistical product and service solutions (SPSS 22). The used technique of PCA was factor-loading matrix obtained from a varimax rotation with Kaiser normalization of main components.

Results and discussion

The impact of 3 tested rhizobacterial strains (B. subtilis, B. polymyxa, and B. megaterium), Eugenol, and A. cina leaves extract on patho-physiological changes of wheat plants under stem rust stress was studied under laboratory and greenhouse conditions.

Microscope examination

Effect of the tested treatments on spore germination and disease symptoms

The effect of whole culture of the 3 Bacillus strains, Eugenol, and A. cina extract on spore germination of P. graminis on water agar medium was shown in Fig. 1. B. subtilis and Eugenol treatments had a higher impact for inhibition of spore germination than the control (Fig. 1b, f). On the other hand, spores treated with B. megaterium showed the highest germination percentage (Fig. 1d). Microscopic examinations of urediniospores exhibited abnormalities, lysis, collapse, and shrinking as a direct effect of the B. subtilis (b), B. polymyxa (c), B. megaterium (d), Eugenol (f), and Artemisia extract 2% (e) compared to (a) the control treatment (Fig. 2). It is well known that some Bacillus species produce extracellular metabolites such as lipopeptides and peptides with antibiotic activity and could be used as antagonists or growth promoters (Romero et al. 2008). Swelling and enlargement of mycelium were reported using lipopeptides by modification of the fungal membrane permeability and lipid composition.

Fig. 1

Light microscopy of P. graminis urediniospores germination on water agar medium with five treatments. a Control (untreated), bB. subtilis, cB. megaterium, dB. polymxa, eArt. 2%, and f Eugenol

Fig. 2

Light microscopy of P. graminis on wheat leaves sprayed with five treatments. a Control (untreated), bB. subtilis, cB. megaterium, dB. polymxa, eArt. 2%, and f Eugenol. b, c, d, and f Abnormalities, lysis, collapse, and shrinking of urediniospores were found in the treatments

The inhibiting effect on spore germination of stem rust pathogen is mainly due to antibiosis. Bacillus spp. produce at least 66 different antibiotic components (Ferreira et al. 1991). These antifungal materials inhibited growth of the pathogenic fungi and consequently reduced the disease. B. subtilis inhibited the growth of a wide range of fungal species including those in the Ascomycetes and Deuteromycetes (Qiao 2006). Likewise, E1R-j strain of B. subtilis inhibited urediniospores germination and germ tubes of P. striiformis in wheat (Li et al. 2013). The mycelial growth of Botrytis cinerea and Sclerotinia sclerotiorum were sensitive to Eugenol (Wang et al. 2010). Also, the inhibition of P. triticina urediniospores germination in vitro was achieved by using some plant extracts, i.e., Jacaranda mimosifolia, Thevetia peruviana, and Calotropis procera (Naz et al. 2014), while the selected treatments, i.e., Art. 2% + Zn, Art. 2% + Mn, Art. 2% + Fe, Art. 2% + Cu, Art. 1% + 50% Sumi-8, and Art. 1%, prevented spore germination of P. triticina (Omara et al. 2015). These results are in agreement with the obtained results, which clearly showed that the Bacillus strains, Eugenol, and A. cina extract significantly suppressed spore germinations of P. graminis on water agar medium with abnormalities and malformation of urediniospores.

Greenhouse studies

Effect of the tested treatments on incubation, latent periods, and infection type

The effects of the 3 bioagents and the 2 natural materials on stem rust development, such as incubation, latent periods, and infection type, were shown in Figs. 3 and 4. Different treatments gave significant differences when sprayed 24 h before and 24 h before and after inoculation of all parameters at 7 days from planting. Incubation and latent periods were increased in B. subtilis and Eugenol treatments. Besides, both treatments achieved the lowest infection type compared to the control. These results might be due to that Bacillus spp. produce several antibiotic compounds that are responsible of these changes in stem rust parameters (Ferreira et al. 1991). On the other hand, the incubation and latent periods as well as the infection type increased slowly in the B. megaterium treatment than the control treatment (Figs. 3 and 4). Likewise, the application of B. subtilis, T. viride, and plant extracts significantly increased both incubation and latent periods of leaf rust, caused by P. triticina f. sp. tritici (Omara et al. 2015 and 2019). Moreover, a foliar spray application at 24 h before and after inoculation was the best application on the seedling disease parameters, incubation and latent periods and infection type compared to application 24 h before inoculation.

Fig. 3

Effect of three bioagents and two natural materials on stem rust development (incubation, latent periods, and infection type) at seedling stage

Fig. 4

Effect of three bioagents and two natural materials on infection type of stem rust, a 24 h before inoculation and b 24 h before and after inoculation

The positive effects on both incubation and latent periods might be due to the induction of systemic resistance (ISR) as a main mechanism of plant response (Loeffler et al. 1986). Furthermore, the application of bioagents could positively alter the physical and mechanical strength of cell walls and adjust the physiological and biochemical responses of wheat plants, which can enhance the biosynthesis of defense-associated molecules that play a key role in delaying the inoculation and latent period of P. graminis. Additionally, Bacillus spp. have numerous approaches to control the disease such as the production of antifungal compounds, nutrient competition, and the induction of systemic resistance (Urszula et al. 2004).

Effect of the tested treatments on pustule size and receptivity (no. of pustules) of P. graminis at seedling stage

Figure 5 shows the reduction in pustule length, pustule width, and receptivity of P. graminis in different treatments. Both B. subtilis and Eugenol gave the lowest pustule length, pustule width, and receptivity than the control (untreated). In contrast, the B. megaterium treatment showed the lowest reduction in pustule length, pustule width, and receptivity. These results could be due to the production of antibiotics by B. subtilis such as bacillin, bacillomycin, bacitracin, mycosubtilin, subenolin, subsporin, and subtilin (Loeffler et al. 1986) reducing the development of the disease and pustule size. In addition, the membrane binding and permeability alteration were reported in Eugenol treatments leading to destabilization and disruption of the plasma membrane (Wang et al. 2010).

Fig. 5

Effect of treatments on pustule length and pustule width and receptivity of P. graminis urediniospores at seedling stage

Laboratory studies

Antioxidant defense enzymes and electrolyte leakage

The activities of antioxidant defense enzymes including catalase (CAT), peroxidase (POX), and polyphenol oxidase (PPO) were displayed in Fig. 6a–c. Bacillus subtilis and Eugenol treatments resulted in a higher activity of CAT, POX, and PPO than control plants at 24, 72, and 168 h, but the highest increase was recorded at 72 h. These enzymes may participate in the responding defense reaction by induction of plant resistance against the pathogenic agents (Ray et al. 1998). Likewise, utilization of Bacillus spp. stimulated the enzymatic activities of chitinase, POX, and PPO against Rhizoctonia damping-off of snap bean plants (Ahmed 2016).

Fig. 6

Activity of catalase, peroxidase, polyphenoloxidase enzymes, and electrolyte leakage in wheat leaves infected with Puccinia graminis and treated with five treatments after 24, 72, and 168 h for two applications

Catalase (CAT) as one of the oxidative enzymes plays an important role for increasing host resistance to control plant pathogens (Liau and Lin 2008). The increased activity of catalase prevented the increase of cytosolic hydrogen peroxide that creates toxic conditions leading to preventing pathogen spread and acting as a secondary signal for defense gene expression and activation of systemic acquired resistance (Neamat et al. 2016). Peroxidase is the first enzyme exhibiting changes in its activity under environmental stress (Milavec et al. 2001). Moreover, the changes in this antioxidant enzyme are known to be directly involved in the activation of plant defense responses. POX is known to catalyze the final polymerization step of lignin synthesis and is directly associated with the increased ability of systemically protected tissues for lignification (Chittoor et al. 1999). Therefore, the peroxidase activity could be used as a good indicator for plant resistance to diseases (Hameed et al. 2011). Also, PPO plays an important role in plant defense via the oxidation of endogenous phenolic compounds to the toxic quinines, which are toxic to the invading pathogens (Thakker et al. 2011). It may also participate in the inducible defense reaction and hypersensitivity for inducing resistance of plants to fungi, viruses, and bacteria (Hanifei et al. 2013).

As for electrolyte leakage, all treatments resulted in a clear reduction in electrolyte leakage in wheat plants infected with stem rust compared to control plants (Fig. 6d). These results may be due to the effect of the pathogen on the plasma membrane in control plants that increases the permeability of the plasma membrane. B. subtilis and Eugenol treatments were the best in decreased electrolyte leakage compared to the untreated plants. Plant stresses such as salinity, pathogen attack, drought, heavy metals, hyperthermia, and hypothermia accompanies electrolyte leakage (EL) as a mechanism of defense response.

Electrolyte leakage (EL) is an indication of increased permeability of the plasma membrane in the control plants than other treatments (Fig. 6d). The plasma membrane in the treatments was not affected by the infection, and its permeability was not increased (Omara et al. 2015). EL is related to K+ efflux from plant cells, which mediated by plasma membrane action conductance (Demidchik et al. 2014). The results were consistent with those obtained by Omara and Abdelaal (2018).

Characterization of B. subtilis metabolites by GC-MS analysis

Due to the performance of B. subtilis compared with other evaluated bioagents, MEMs (Micro-Electro Mechanical Systems) GC-MS technology was used to identify its active compounds. The most peak numbers and peak areas of compounds excreted by B. subtilis belonged to ten compounds. These compounds mostly included fatty acids known as 9-octadecanoic acid, octadecanoic acid, oleic acid, n-hexadecanoic acid, and hexadecanoic acid (Fig. 7).

Fig. 7

Metabolites structural (a) and its molecular formula (b) extracted by GC-MS analysis of B. subtilis

Generally, numerous members of Bacillus species are known as producers of lipopeptides belonging to the surfactin, iturin, and fengycin families (Zuber et al. 1993). Fengycin is an antifungal lipopeptide complex produced by B. subtilis F-29-3 (Vanittanakom and Loeffler 1986). It consists of 2 main components, fengycin A and fengycin B. The lipid moiety of both analogs was more variable as fatty acids and identified as anteiso-pentadecanoic acid (ai-C15), iso-hexadecanoic acid (i-C16), and n-hexadecanoic acid (n-C16). There is an evidence for further saturated and unsaturated residues up to C18. In the present study, these components of fatty acids were detected in supernatant analysis, using GC-MS in case of B. subtilis. These results were consistent with those of Belal et al. (2013) who found that the methanolic extract of B. subtilis contained fatty acids such as nonanoic acid, decanoic acid, dodecatrienoic acid, heptadecanoic acid, octadecanoic acid, pentadecanoic acid, hexadecanoic acid, and some of their derivatives (Belal et al. 2013).

Principal component analysis (PCA)

Principal component analysis was performed on incubation and latent periods, infection type, pustule length, pustule width, receptivity (no. of pustule), catalase (CAT), peroxidase (POX), polyphenoloxidase (PPO), and electrolyte leakage in response to artificial infection of wheat stem rust and treatment with three Bacillus strains, Eugenol, and A. cina extract (Fig. 8a, b). Interpretation of the principal components (PCs) was aided by inspection of the factor-loading matrix extracted from a varimax rotation with Kaiser normalization of main components to identify factors responsible for the grouping of the dataset. As shown from scree plot graph of eigenvalues and loadings plot (Fig. 8), these 2 components, incubation and latent periods, have eigenvalues more than one. Therefore, these 2 components were extracted and describing approximately 96.595% of total variation; the remaining was 3.405% distributed on 8 factors. So, the variation of these factors is very small and negligible. Accordingly, principal component analysis gave an evidence to the importance of incubation and latent periods, as they were considered a good and more reliable indicator for evaluation of these materials. Summing up the results, the factor-loading matrix, extracted from a varimax rotation with Kaiser normalization, gave clear evidence to the importance of all parameters in this study, especially incubation and latent periods. Similar results were previously obtained when correlation statistics were performed between different disease parameters of wheat rusts and grain yield of the studied wheat genotypes (Abu Aly et al. 2017).

Fig. 8

The scree plot of eigenvalue (a) and loadings plot (b) for incubation and latent periods, infection type, pustule length, pustule width, catalase, peroxidase, polyphenoloxidase enzymes, and electrolyte leakage in response to wheat stem rust. A, incubation period; B, latent period; C, infection type; D, no. of pustule; E, pustule length; F, pustule width; G, catalase; H, peroxidase; I, polyphenoloxidase; and J, electrolyte leakage

Conclusion

The present study assured the promising capability of the tested microbial agents and natural materials in controlling wheat stem rust disease. Although the used chemical control surpassed biocontrol agents in the efficacy of disease inhibition, the bioagents have other important environmental advantages with high considerations. Thus, for environmental safety, further study is needed before the broad commercial use of these antagonistic microorganisms.