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Biological control of cucumber powdery mildew (Podosphaera xanthii) (Castagne) under greenhouse conditions


Cucumber powdery mildew disease caused by Podosphaera xanthii (Castagne) U. Braun & Shishkoff severe disease-causing yield losses worldwide. This research study was conducted to evaluate the efficacy of the tested bio-agents, Trichoderma harzianum, T. viride, Bacillus subtilis, Paenibacillus polymyxa, and Serratia marcescens, as well as the fungicide score (Difenoconazole), on cucumber infected with P. xanthii, in vitro and under greenhouse conditions. Results indicated that culture filtrate of the tested bio-agents and the fungicide (control) significantly reduced P. xanthii conidial germination in vitro; the reduction percentage ranged between 91.17 and 76.06%. Also, score recorded the highest reduction percentage (97.19%). All treatments significantly decreased the disease severity and area under disease progress curve (AUDPC) post spraying the bio-agents on cucumber plants under greenhouse conditions. Score followed by B. subtilis significantly decreased disease severity percentage (67.33 and 65.38%, respectively) and AUDPC (322.84 and 342.06) than the untreated control (988.13 AUDPC). Additionally, treated cucumber plants showed a significant increase in plant growth parameters (plant height, total chlorophyll, fresh, and dry weight) and yield parameters (fruit number/plant and fruit weight/plant) as well the activity of defense-related enzymes, i.e., peroxidase (PO) and polyphenol oxidase (PPO), and total phenols content (TPC) compared to the untreated plants.


Cucumber (Cucumis sativus L.) is one of the most widely grown greenhouse crops. Powdery mildew is caused by Podosphaera xanthii (Castagne) U. Braun & Shishkoff (formerly Sphaerotheca fuliginea (Schlechend.: Fr) Pollacci). It is a major foliar disease worldwide, reducing crop quality and yield (Rur et al. 2018).

Fungicides are one of the principal tools for managing cucumber powdery mildew (Lebeda et al. 2010). However, due to the harmful effects on the environment because of the use of fungicide (Ozkara et al. 2016), biological control is an important alternative to reduce risk and diminish the hazardous effects of the fungicides application that achieved remarkable success in plant diseases and powdery mildew disease control (Tanaka et al. 2017; Rur et al. 2018).

Applications of plant growth-promoting rhizobacteria (PGPR) as biotic inducers have a potential in controlling plant diseases (O’Brien 2017). This positive performance of PGPR has a direct and indirect effects on plants, direct promotion by production of metabolites that improves the plant growth, and indirect growth effects by removal of the pathogens via the secondary metabolites production (Sarhan and Shehata 2014; Prasannath 2017).

Induced systemic defense reaction, using PGPR, in plants is one important means for management plant diseases as it can induce plant defense in the host plants in response to fungal infection including defense-related enzymes and pathogenesis-related proteins, indoleacetic acid (IAA), lignin synthesis, and phenolic compounds accumulation (Reddy et al. 2014; Prasannath 2017).

Defense-related enzyme PO and PPO are mentioned as the plant induced systemic resistance (ISR) that correlates with the disease control (El-Sharkaway et al. 2014; Prasannath 2017; Elsisi 2019). These enzymes result in the biosynthesis of plant metabolites such as phenolic compounds, flavonoids, tannins, and lignin (Prasannath 2017; Singh et al. 2018). These products can provide defense in plants against pathogenic attack (Hahlbrock and Scheel 1989). Many studies have indicated that the increase of defense-related enzymes activity due to greater accumulation of phenolics can offer protection against plant diseases (Hafez et al. 2018; Elsisi 2019).

Many investigators demonstrated the application of biological control against cucumber powdery mildew disease (El-Sharkaway et al. 2014; Rur et al. 2018; Punja et al. 2019). The applications of bio-agents were effective in controlling cucumber powdery mildew development through inhibition of the conidial germination and mycelial growth rate of the pathogen decreased percent of infected leaf area (El-Naggar et al. 2012; Rur et al. 2018; Punja et al. 2019).

The objectives of the present study were to evaluate the efficacy of some biotic inducers on inducing resistance to cucumber plants against powdery mildew under the greenhouse conditions and the reaction of host metabolic, i.e., defense-related enzymes and phenolic compounds and cucumber plants growth parameters and yield.

Materials and methods

Source of bio-agents

The tested fungal bio-agents, i.e., Trichoderma harzianum and T. viride, and tested bacterial bio-agents, i.e., Bacillus subtilis, Paenibacillus polymyxa, and Serratia marcescens, were obtained from the Microbiology Dept, Soil, Water and Environment Res. Inst, (SWERI), Agricultural Research Center, Giza, Egypt.

Preparation of tested bio-agents inocula

T. harzianum and T. viride strains were grown for 10 days on PDA medium and then separately. Their spore’s suspensions were prepared and adjusted, using hemocytometer slide, to 107 spore ml−1 with sterilized water. B. subtilis, P. polymyxa, and S. marcescens strains were grown separately in flasks; 250 ml contained nutrient liquid medium for 3–4 days on an orbital shaker at 150 rpm. The suspension of each bacterial strain was adjusted at 109 cell ml−1 using a hemocytometer slide.

Fungicide score 25% EC

Common name: difenoconazole, chemical name: dimethyl [1-((2-(2-chloro-4-(4-chlorophenoxy) phenyl)-4-methyl-1,3-dioxolan-2-yl) methyl)-1H-1,2,4-triazole)], and recommended dose 50 ml/l00 l (Syngenta Crop Protection AG. Basel, Switzerland).

Efficacy of tested bio-agents culture filtrates on spore germination of Podosphaera xanthii

Viable P. xanthii conidial spores were obtained by softly shaken by a glass rod from young sporulating lesions (Godwin et al. 1987). Newly collected spores were placed on glass slides previously cleaned by ethyl alcohol and air-dried as described by Nair and Ellingboe (1962). Slides were covered by thin layers of water agar 2%, amended by the filter-sterilized culture filtrate of the tested bio-agents. The slides, covered by agar-free culture filtrate, were used as a control then, laid over glass rods in sterilized Petri dishes, containing numerous filter papers fully water-moistened and incubated under continuous light at 25 °C for 24 h (Reifschneider et al. 1985). Spore produced a germ tube as long as the width considered being germinated. Spores were microscopically examined at × 40 magnifications to determine germination. Percentages of spore germination were calculated for 100 spores (Menzies et al. 1991). Three replicates were examined for each treatment.

Greenhouse experiments

Experiments were carried out under plastic greenhouse conditions (40 m × 9 m) in randomly complete block design during the seasons of 2019 at Dahshour, Giza Governorate, Egypt, using cucumber hybrid F1 Sinai1. Rectangular plastic trays (5 × 5 × 7 cm) were filled by autoclaved commercial potting medium (a mix of peat moss, vermiculite). Cucumber seeds were sown in trays and covered with layers (3 cm) of sterile sand. Seven treatments with 3 replicates per treatment were carried out. Each replicate contained 12 plants. Seedlings were transplanted after 3 weeks, on the 2 sides of the ridge, at a spacing of 50 cm between them within the row. The plants were distributed in 3 rows; each was 0.7 m wide and 2 m length. Plants were fertilized by recommended doses.

Artificial inoculation was conducted under greenhouse conditions by freshly collected conidia of P. xanthii suspension (105conidiaml−1) performed according to Kamel (2003). Three weeks old cucumber plants were sprayed by spore suspension of P. xanthii, about 15 ml of spores’ suspension. Then, the inoculated cucumber plants were covered by plastic sheets for 24 h to keep high humidity levels (El-Sharkaway et al. 2014). In addition, plants were sprayed by the previously prepared fungal and bacterial bio-agents strains as well as the fungicide at the previously mentioned dose. Control treatment was sprayed by sterilized tap water.

Disease assessment

Disease severity was estimated at 5 days intervals for 20 days post inoculation transplanting. Plants were examined periodically for symptoms appearance, and disease severity was measured, using the 0–11 scale as mentioned by Horsfall and Barrett (1945). Ten random plants were used for each replicate. The severity of powdery mildews was measured, using the following formula:

Disease severity (%) = Σ (n × v)/11 N × 100

where n = number of infected leaves in each category; v = numerical values of each category; and N = total number of the infected leaves.

The mean (AUDPC) was calculated, using the formula of Pandy et al. (1989).

AUDPC = D [1/2(Y1 + Yk) + (Y2 + Y3 + . . …… + Yk − 1)]

where D = time interval; Y1 = first disease severity; Yk = last disease severity; and Y2, Y3, Yk−1 = intermediate disease severity.

Chlorophyll content measurements

Total chlorophyll contents were determined in the 5th apical fully expanded leaf, using the greenness measurements, portable leaf chlorophyll meter SPAD-501 (Minolta Corp) Yadava (1986).

Evaluation of growth and yield parameters

Growth and yield parameters were determined/plant. The average leave numbers/plant and leaf area was determined at 50 days in the experimental plants. Measurement of plant leaf area was carried out, using the CI-202 Portable Laser Leaf Area Meter CID (Bio-Science, Inc 1554 NE 3rd Avenue, Camas, WA, 98607, USA). Leaf area was measured as square centimeters. The average fruit numbers and fresh weight/plant were assessed by harvesting the fruits every 2 days, while the fruits at the marketable size, for 90 days after transplanting. Yield was expressed as fruits number and weight/plant.

Biochemical assays

Peroxidase (PO), polyphenol oxidase (PPO) activity, and total phenol content (TPC) were determined in tissues on bio-agents treated cucumber leaves as well as in the untreated control treatment.

Samples’ collection

Samples were collected at 6 days post inoculation with the pathogen and then grounded with liquid nitrogen (L-N2) as fine powder with a mortar and pestle. One gram of the grounded tissues was mixed with 1 ml of extraction buffer phosphate, pH 6.0 according to Bollage et al. (1996). Samples were vortexed and centrifuged at 8000 rpm for 25 min under 4 °C. Then, clear supernatant (crude enzyme source) was kept at – 20 °C for further studies (Biles and Martyn 1993).

Determination of peroxidase

Activity of PO was determined according to Allam and Hollis (1972) spectrophotometrical method in absorbance at 430 nm/g fresh weigh/15 min. PO activity was expressed as enzyme unit/mg protein/min.

Determination of polyphenol oxidase

Activity of PPO was determined according Ishaaya (1971) spectrophotometrical method at an absorbency of 405 nm. PPO activity was expressed as enzyme unit/mg protein/min.

Determination of total phenols contents

One gram was extracted at 70 °C for 15 min by 10 ml of 80% methanol of cucumber leaves sample. TPC was determined using the method described by Zieslin and Ben-Zaken (1993) Folin-Ciocalteu reagent colorimetric analysis method. TPC amount was expressed as microgram GAE/g fresh weight.

Statistical analysis

The Wasp software (Web Agriculture Stat Package) was used to the ANOVA statistical analysis of the data. According to Duncan’s multiple range tests, at P ≤ 0.05, all measurements and comparisons mean values were determined (Gomez and Gomez 1984).

Results and discussion

Effect of tested bio-agents culture filtrate on conidial germination of P. xanthii

The efficacy of the tested bio-agents culture filtrate T. harzianum, T. viride, B. subtilis, P. polymyxa, and S. marcescens as well as the fungicide score (25% EC) was evaluated as percentage of P. xanthii conidial germination in vitro.

Results shown in Table 1 indicate that all culture filtrate of the tested bio-agents significantly inhibited the conidial germination of P. xanthii, in vitro. The highest reduction was attributed to the fungicide being (97.19%), followed by B. subtilis (91.17.0%), P. polymyxa (88.47%), and S. marcescens (85.46%) whereas, T. viride and T. harzianum recorded (82.13% and 76.06%) reduction, respectively.

Table 1 Effect of bioagent culture filtrate on Podosphaera xanthii conidial germination, 24 h after treatment and incubation at 28 ± 1 °C

In the present study, the strong inhibitory action against P. xanthii spore germination revealed a strong antifungal activity of the tested bio-agents. This antifungal activity suggested the production of antibiotic(s), and/or another direct inhibitory substances as hydrolytic enzymes, hydrogen cyanide, or siderophore (Sarhan and Shehata 2014; Rais et al. 2017; Prasannath 2017; Tanaka et al. 2017). Such results are in harmony with those previously obtained by García-Gutiérrez et al. (2013), El-Sharkaway et al. (2014), Tanaka et al. (2017), Hafez et al. (2018), and Elsisi (2019) who showed the ability of the bio-agents to inhibit powdery mildew conidial spores germination.

Effect of tested bio-agents on controlling powdery mildew on cucumber plants

Results presented in Table 2 showed that all the tested bio-agents decreased area under disease progress curve (AUDPC) than the control. B. subtilis achieved the highest efficiency in reducing disease severity and decrease of AUDPC, being 65.38% efficiency and 342.06 AUDPC for powdery mildew, followed by P. polymyxa, and then S. marcescens, T. harzianum, and T. viride being 61.00, 52.44, 44.07, and 39.72% efficiency and 385.38, 469.93, 552.63, and 595.61 AUDPC, respectively, compared to the control (988.13 AUDPC). The fungicide recorded the highest efficiency (67.33%) and AUDPC being 322.84.

Table 2 Effect of bioagent treatments on powdery mildew (Podosphaera xanthii) disease severity (DS %) and (AUDPC) of cucumber plants

These results are in agreement with many previous studies, indicated the effective of bio-agents Bacillus spp. and Trichoderma spp. for controlling cucumber powdery mildew disease (El-Naggar et al. 2012; Sawant et al. 2017; Tanaka et al. 2017; Punja et al. 2019). This reduction may be due to the potential of the tested bio-agents as PGPR, which is widely applied for controlling plant diseases (Sarhan and Shehata 2014; Prasad et al. 2017). Recently, numerous successful researches investigated several bio-agents such as Serratia spp., Bacillus spp., and Trichoderma spp. for protection against airborne pathogens particularly powdery mildew disease. El-Kot and Derbalah (2011) indicated that by producing antifungal compounds, Trichoderma spp. reduced the squash powdery mildew disease severity. El-Naggar et al. (2012) found that T. viride significantly reduced cucumber powdery mildew disease. El-Sharkaway et al. (2014) found that spraying cucumber plants with the bio-agents, B. subtilis, Pseudomonas fluorescens, Derxia gummosa, and T. harzianum, significantly reduced the severity of both cucumbers powdery and downy mildew diseases. Tanaka et al. (2017) demonstrated that production of the antibiotic prumycin was a major factor in biocontrol by Bacillus amyloliquefaciens against powdery mildew of cucumber. Hafez et al. (2018) found that a significant reduction in the squash powdery mildew severity, and (AUDPC) in infected plants treated with the bio-agents, i.e., B. pumilus, B. megaterium, B. subtilis, B. chitinosporus, P. polymyxa, T. harzianum, and T. viride. These results are in accordance with Elsisi (2019) who found that spraying squash plants with the bio-agents B. subtilis, P. polymyxa, T. harzianum, T. viride, T. hamatum, and T. album decreased the powdery mildew incidence and the severity under greenhouse conditions. Punja et al. (2019) demonstrated that the application of the biocontrol agent B. subtilis on greenhouse cucumber plants either preventative or eradicative treatments reduced the powdery mildew disease incidence and severity.

Effect of tested bio-agents on chlorophyll content and growth parameters of cucumber plants

Data in Table 3 showed that chlorophyll content and growth parameters (leaf area and the number of leaves) significantly increased in cucumber plants treated with the tested bio-agents. Highest chlorophyll content was recorded in cucumber plants treated with the fungicide (44.90), followed by B. subtilis, P. polymyxa, S. marcescens, T. viride, and T. harzianum (43.90, 41.40, 38.85, 35.30, and 30.75, respectively) compared to the untreated control (25.30). The numbers of leaves/plant and leaf area significantly increased in the treated cucumber plants. The fungicide recorded the highest number of leaves/plant (37.0), followed by B. subtilis, P. polymyxa, S. marcescens, T. viride, and T. harzianum (36.4, 35.0, 32.7, 27.5, and 22.9, respectively) than the untreated control plants (21.3). As well, the fungicide and B. subtilis recorded the maximum leaf area (361.3 and 352.3 cm2), followed by P. polymyxa, S. marcescens, T. viride, and T. harzianum (347.3, 337.0, 324.7, 324.7, and 269.0 cm2, respectively) than the control plants (208.0 cm2).

Table 3 Effect of bioagent treatments on chlorophyll content and growth parameters of powdery mildewed cucumber plants

Obtained results are in harmony with many investigators who stated that the improvement of plant growth parameters regarded to the role of the PGPR that has an important role in the resistance to infection with diseases and consequently, improved growth parameters (Reddy et al. 2014; Singh et al. 2018). Treated mildewed cucumber or squash plants with the bio-agents, Bacillus spp., Serratia spp., and Trichoderma spp., significantly increased chlorophyll content and growth parameters/plant (El-Sharkaway et al. 2014; Hafez et al. 2018). Youssef et al. (2018) found that treated tomato leaves with the bioagent Serratia proteamaculans significantly increased chlorophyll content higher than the untreated control plants.

Effect of bio-agents on yield parameters of cucumber plants

Data in Table 4 revealed that yield parameters significantly increased in mildewed cucumber plants sprayed with the tested bio-agents. The fungicide recorded the highest fruit number/plant being (37.7 fruit/plant) with an average increase of 59.07% more than the control plants (23.7 fruit/plant), followed by B. subtilis (35.7 fruit/plant), P. polymyxa (33.3 fruit/plant), S. marcescens (32.0 fruit/plant), T. viride (31.3 fruit/plant), and T. harzianum (30.7 fruit/plant), with an average increase of 50.63, 40.51, 35.02, 32.07, and 29.54% than the control, respectively. Similarly, fruits yield/plant markedly increased than the control. The fungicide and B. subtilis showed the highest fruits yield (3.65 and 3.50 kg/plant), with an average increase of 100.55 and 92.31% over the control, followed by P. polymyxa (3.20 kg/plant), S. marcescens (2.95 kg/plant), T. viride (2.75 kg/plant), and T. harzianum (2.45 kg/plant), with an average increase of 75.82, 62.09, 51.10, and 34.62%, respectively.

Table 4 Influence of bio-agents treatments on yield parameters of powdery mildewed cucumber plants

Additional mechanisms by which these PGPR affect plants involve the production of plant growth regulator (indoleacetic acid, gibberellins, and cytokinin) resulting in stimulation of plant growth and increases in fruits yield (Reddy et al. 2014 and Singh et al. 2018). Obtained results are in harmony with those reported by El-Naggar et al. (2012), García-Gutiérrez et al. (2013), El-Sharkaway et al. (2014), Tanaka et al. (2017), and Elsisi (2019) who found that the biological treatments reduced powdery mildew disease and increased in crop yield.

Effect of some bio-agents on biochemical changes in mildewed cucumber plants

The tested bio-agents (B. subtilis, P. polymyxa, S. marcescens, T. harzianum, and T. viride) as biotic inducers increased activity of the PO and PPO defense-related enzymes as well as the TPC in cucumber leaves infected with powdery mildew disease (P. xanthii). Data in Table 5 showed that the highest activity of PO was induced by B. subtilis (228.3), followed by P. polymyxa, S. marcescens, T. viride, and T. harzianum recording (187.7, 180.0, 169.3, and 155.3), respectively. Meanwhile, the fungicide achieved the least effective one recording (149.7). Similarly, B. subtilis recorded the highest level of the activity of PPO (127.7), followed by P. polymyxa, S. marcescens, and the fungicide score (119.3, 111.7, and 96.3, respectively), whereas the least enzyme activity was recorded by T. viride and T. harzianum, being 84.3 and 83.3. Also, TPC significantly increased in all tested treatments, particularly P. polymyxa (68.7) than the control (24.7), followed by B. subtilis (58.3), S. marcescens (52.7), T. viride (49.7), and T. harzianum (47.3), while the fungicide (45.3) showed the least effect on TPC.

Table 5 Effect of some bio-agents treatments on biochemical changes of powdery mildewed cucumber plants after 6 days from inoculation

Using PGPR, such as Serratia spp., Trichoderma spp., and Bacillus spp., for inducing systemic defense reaction in plants is considered an important approach to suppress plant disease. Induced plant defense responses are directly linked with induction of defense-related enzymes PO and PPO and accumulation of phenolic compounds (Walters et al. 2005; Singh et al. 2018). Many investigators demonstrated the positive relationships between defense-related enzymes and phenolic compounds and resistance to powdery mildew disease. El-Naggar et al. (2012) and El-Sharkaway et al. (2014) indicated that the treatment with bio-agents significantly decreased the powdery mildew disease severity in cucumber plants and induced defense-related enzymes PO, PPO, and increased phenolic compounds. As well, Hafez et al. (2018) and Elsisi (2019) reported that resistance to powdery mildew disease was correlated to the increase of biochemical changes, i.e., defense-related enzymes PO and PPO, and TPC of squash plants as a result after spraying squash plants with the bio-agents under greenhouse conditions.


The present study indicated that the application of bio-agents, i.e., Bacillus spp., Serratia marcescens, and Trichoderma spp., significantly protected cucumber plants against powdery mildew disease, mainly through the induction of systemic resistance. However, the application of such bio-agents in the control of cucumber powdery mildew on the field scale provides a practical environmentally friendly disease management against cucumber disease and can be used through integrated disease management.

Availability of data and materials

All data and materials are available upon request.



Area under disease progress curve


Diseases severity


Emulsifiable concentrate


Gallic acid equivalent


Potato dextrose agar


Plant growth-promoting rhizobacteria




Polyphenol oxidase


Total phenol content


  • Allam AI, Hollis JP (1972) Sulfide inhibition of oxidase in rice roots. Phytopathology 62:634–639

    Article  CAS  Google Scholar 

  • Biles CL, Martyn RD (1993) Peroxidase, polyphenoloxidase, and shikimate dehydrogenase isozymes in relation to tissue type, maturity and pathogen induction of watermelon seedlings. Plant Physiol Biochem 31:499–506

    CAS  Google Scholar 

  • Bollage MD, Rozycki DM, Edelstein JS. (1996) Protein methods. Wiley-Liss;Inc.; New York. 413pp.

  • El-Kot G, Derbalah A (2011) Use of cultural filtrates of certain microbial isolates for powdery mildew control in squash. J Plant Prot Res 51(3):252–260

    Article  Google Scholar 

  • El-Naggar M, El-Deeb H, Ragab S (2012) Applied approach for controlling powdery mildew disease of cucumber under plastic houses. Pak J Agric: Agric Eng Vet Sci 28(1):54–64

    Google Scholar 

  • El-Sharkaway MM, Kamel SM, El-Khateeb NM (2014) Biological control of powdery and downy mildews of cucumber under greenhouse conditions. Egypt J Biol Pest Control 24(2):407

    Google Scholar 

  • Elsisi AA (2019) Evaluation of biological control agents for managing squash powdery mildew under greenhouse conditions. Egypt J Biol Pest Control 29:89

    Article  Google Scholar 

  • García-Gutiérrez L, Zeriouh H, Romero D, Cubero J, Vicente A, Pérez-García A (2013) The antagonistic strain Bacillus subtilis UMAF6639 also confers protection to melon plants against cucurbit powdery mildew by activation of jasmonate- and salicylic acid-dependent defense responses. Microb Biotechnol 6(3):264–274

    Article  Google Scholar 

  • Godwin J, Mansfield J, Darby P (1987) Microscopical studies of resistance to powdery mildew disease in the hop cultivar Wye Target. Plant Pathol 36(1):21–32

    Article  Google Scholar 

  • Gomez K.A. and Gomez A.A. (1984) Statistical procedures for agriculture research. Second Ed., p.680. A Willey Inter. Science Publication, John Willy of Sons. Inc. New York, USA.

  • Hafez YM, El-Nagar AS, Elzaawely AA, Kamel S, Maswada HF (2018) Biological control of Podosphaera xanthii the causal agent of squash powdery mildew disease by upregulation of defense-related enzymes. Egypt J Biol Pest Control 28(1):57

    Article  Google Scholar 

  • Hahlbrock K, Scheel D (1989) Physiology and molecular biology of phenylpropanoid metabolism. Annu Rev Plant Physiol Plant Mol Biol 40:347–369

    Article  CAS  Google Scholar 

  • Horsfall HAJ, Barrett RW. (1945) An improved grading system for measuring plant diseases. (Abstract) Phytopathology, 35: 655.

  • Ishaaya I (1971) In the armored scale Aonidiella aurantii and observation on the phenoloxidase system Chrysomphalus aonidum. Comp Biochem Physiol 39(B):935–943

    CAS  Google Scholar 

  • Kamel SMH (2003) Antagonistic effects of some microbial inhabitants on phylloplane of squash plants towards Sphaerotheca fuliginea. M.Sc. Thesis, Fac. Agric. Tanta Univ. Egypt. pp. 94

  • Lebeda A, McGrath MT, Sedlakova B (2010) Fungicide resistance in cucurbit powdery mildew fungi. Fungicides:221–246

  • Menzies JG, Ehret DL, Glass ADM, Helmer T, Koch C, Seywerd F (1991) Effects of soluble silicon on the parasitic fitness of Sphaerotheca fuliginea on Cucumis sativus. Phytopathology 81:84–88

    Article  Google Scholar 

  • Nair KRS, Ellingboe AH (1962) A method of controlled inoculations with conidio spores of Erysiphe graminis var. tritici. Phytopathology 52:417

    Google Scholar 

  • O’Brien PA (2017) Biological control of plant diseases. Australasian Plant Pathol 46(4):293–304

    Article  Google Scholar 

  • Ozkara A, Akyıl D, Konuk M (2016) Pesticides, environmental pollution, and health. In: Larramendy, M.L., Soloneski, S. (Eds.), Environmental health risk - hazardous factors to living species, pp. 3-27

    Google Scholar 

  • Pandy HN, Menon TCM, Rao MV (1989) Simple formula for calculating area under disease progress curve. Rachis. 8(2):38–39

    Google Scholar 

  • Prasad RM, Sagar BV, Devi GU, Triveni S, Rao SRK, Chari DK (2017) Isolation and screening of bacterial and fungal isolates for plant growth promoting properties from tomato (Lycopersicon esculentum Mill.). Int J Curr Microbiol App Sci 6(8):753–761

    Article  Google Scholar 

  • Prasannath K (2017) Plant defense-related enzymes against pathogens: a review. AGRIEAST: J Agric Sci 11(1):38–48

    Article  Google Scholar 

  • Punja ZK, Tirajoh A, Collyer D, Ni L (2019) Efficacy of Bacillus subtilis strain QST 713 (Rhapsody) against four major diseases of greenhouse cucumbers. Crop Prot 124:104845

    Article  Google Scholar 

  • Rais A, Jabeen Z, Shair F, Hafeez FY, Hassan MN (2017) Bacillus spp., a bio-control agent enhances the activity of antioxidant defense enzymes in rice against Pyricularia oryzae. PLoS One 12(11):e0187412

    Article  Google Scholar 

  • Reddy M, Ilao RI, Faylon PS (2014) Recent advances in biofertilizers and biofungicides (PGPR) for sustainable agriculture. Cambridge Scholars Publishing, Newcastle upon Tyne, NE6 2XX, p 510

  • Reifschneider FJB, Boitexu LS, Occhiena EM (1985) Powdery mildew of melon (Cucumis melo) caused by Sphaerotheca fuliginea in Brazil. Plant Dis 69:1069–1070

    Google Scholar 

  • Rur M, Rämert B, Hökeberg M, Vetukuri RR, Grenville-Briggs L, Liljeroth E (2018) Screening of alternative products for integrated pest management of cucurbit powdery mildew in Sweden. Eur J Plant Pathol 150:127–138

    Article  Google Scholar 

  • Sarhan EAD, Shehata HS (2014) Potential plant growth-promoting activity of Pseudomonas spp. and Bacillus spp. as biocontrol agents against damping-off in Alfalfa. Plant Pathol J 13:8–17

    Article  CAS  Google Scholar 

  • Sawant IS, Wadkar PN, Ghule SB, Rajguru YR, Salunkhe VP, Sawant SD (2017) Enhanced biological control of powdery mildew in vineyards by integrating a strain of Trichoderma afroharzianum with sulphur. Biol Control 114:133–143

    Article  CAS  Google Scholar 

  • Singh AK, Kumar A, Singh Pk (2018) PGPR amelioration in sustainable agriculture. Food security and environmental management. 1st Edition. Woodhead Publishing. Page 284

  • Tanaka K, Fukuda M, Amaki Y (2017) Importance of prumycin produced by Bacillus amyloliquefaciens SD-32 in biocontrol against cucumber powdery mildew disease. Pest Manag Sci 73:2419–2428

    Article  CAS  Google Scholar 

  • Walters D, Walsh D, Newton A, Lyon G (2005) Induced resistance for plant disease control: maximizing the efficacy of resistance elicitors. Phytopathology 95(12):1368–1373

    Article  CAS  Google Scholar 

  • Yadava UL (1986) A rapid and non destructive method to determine chlorophyll in intact leaves. Hortic Sci 21:1449–1450

    CAS  Google Scholar 

  • Youssef SA, Tartoura KA, Greash AG (2018) Serratia proteamaculans mediated alteration of tomato defense system and growth parameters in response to early blight pathogen Alternaria solani infection. Physiol Mol Plant Pathol 103:16–22

    Article  CAS  Google Scholar 

  • Zieslin N, Ben-Zaken R (1993) Peroxidase activity and presence of phenolic substances in peduncles of rose flowers. Plant Physiol Biochem 31:333–333

    CAS  Google Scholar 

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The authors would like to thank Prof. Dr. Heba S. Shehata, at Soils Water & Environment Research Institute, Agricultural Research Center, Giza, Egypt.


Funding is by Plant Pathology Research Institute, Agricultural Research Center, and authors.

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Ehab A. D. Sarhan: conception and design of the work; the acquisition, analysis, and interpretation of data; editing the manuscript. Corresponding author. Michael H. F. Abd-Elsyed: the acquisition, analysis, and interpretation of data. Azza M. Y. Ebrahiem: the acquisition, analysis, and interpretation of data. The authors read and approved the final manuscript.

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Correspondence to Ehab A. D. Sarhan.

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Sarhan, E.A.D., Abd-Elsyed, M.H.F. & Ebrahiem, A.M.Y. Biological control of cucumber powdery mildew (Podosphaera xanthii) (Castagne) under greenhouse conditions. Egypt J Biol Pest Control 30, 65 (2020).

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