Skip to main content

Effect of destruxin on the population reduction of green peach aphid Myzus persicae (Hemiptera: Aphididae) and the predator Coccinella undecimpunctata (Coleoptera: Coccinellidae) in tomato fields



Destruxin is the toxin of some entomopathogenic fungi.


The efficiency of two destruxins, Destruxin A-760 and Destruxin A-724, was evaluated against the green peach aphids Myzus persicae (Sulzer) (Hemiptera: Aphididae) pests in tomato plants in two different climatic Governorates El-Sharkia and El Behira. Also, their safety levels to the predator Coccinella undecimpunctata L (Coleoptera: Coccinellidae) were studied under laboratory and field conditions.

Materials and methods

Two destruxin were applied on the target pests and its predators under laboratory and field conditions. Six aqueous concentrations of the two destruxin were prepared: 2.000–0.125 ppm. One day, adults of C. undecimpunctata and second instar nymphs of M. persicae were used for evaluation of the pathogenicity and efficacy of Destruxin A-760 and Destruxin A-724. This was accomplished by different techniques, a spray technique to evaluate contact effect and a feeding technique to evaluate oral toxicity.


Results showed that, under laboratory conditions, LC50 values for Destruxin A-760 and Destruxin A-724 were 58 and 66 ppm, respectively against M. persicae. Under field conditions, the percentages of infested plants with M. persicae were significantly decreased after treatments with both Destruxin A-760 and Destruxin A-724 as compared with the corresponding controls. In Nobaryia, weights of tomato yield were 3158 and 3988 kg/feddan (F) when Destruxin A-760 and Destruxin A-724 whereas the control yielded 2169 kg/F in the corresponding controls, respectively. While the corresponding yield in EL Sharkia (Zagazig) were 3569 and 3599 kg/F following the same order as compared to 2169 ± 36.82 and 2000 ± 80.54 kg/ F, respectively in the control. The study showed that C. undecimpunctata exhibits relatively high and reasonable resistance to Destruxin A-760 and Destruxin A-724 at their highest lethal concentration (LC) (i.e., 44 ppm) for treated insects.


The tomato crop (Lycopersicon esculentum) is an important vegetable crop in Egypt; it belongs to Solanaceous. This plant is usually infested in Egypt with many destructive pests, especially the most destructive one which is the green peach aphid, Myzus persicae Sulzer (Hemiptera: Aphididae) Blackman and Eastop (2006). These pests transmit several viruses to many economic crops (Namba and Sylvester 1981; Berry 1998). This species causes great damages and diseases to the leaves and fruits (Filotos et al. 2004). M. persicae is a small green aphid causing a decrease in growth, shriveling of the leaves, and the death of various tissues (Namba and Sylvester 1981; Berry 1998). The green peach aphid is found worldwide, although it is less tolerant of colder climates and over winters through its eggs, which are laid in trees of the genus Prunus (Howe and Jander 2008). Destruxin is the toxin of the fungi (Metarhizium anisopliae). This toxin causes death to many serious pests, which exhibit a variety of insecticidal actions (Roberts 1981).

The toxin called destruxin is a cyclic hexadepsipeptide produced by the fungus Metarhizium anisopliae. Destruxin (DEX) causes paralysis and a speedy death to the harmful pests and also it causes suppression of the insect immune system (Odier et al. 1992). Also, destruxin causes an inhibitory activity on the leukemic cell production, decreasing the number of cells in G2/M phase (Odier et al. 1992). Destruxins (DEX) cyclic hexadepsipeptide mycotoxin which have insecticidal and phytotoxic activity. Sabbour and Shaurub (2018) found that the destruxin treatments and nano destruxin decrease the infestations with S. littoralis under laboratory conditions. Under field conditions, the nano destruxin significantly decreased the infestations number of S. littoralis in the cotton field. Thungrabeab and Tongma (2007) reviewed the research of several authors dealing with the differential susceptibilities of many natural enemies to various fungal species. They concluded that some genera or species of fungi could be specific and might inflict only certain types of hosts. They also mentioned that the fungus Beauveria bassiana was not pathogenic to Coccinella undecimpunctata and Chrysoperla carnea.

The present work aims to evaluate the efficacy of destruxin against M. persicae and their main efficient predator (C. undecimpunctata) in tomato fields in Egypt.

Materials and Methods

Insect cultures


M. persicae were reared on small potted tomato plants inside cylindrical glass cages (15-cm diameter × 40-cm height), covered with muslin, under controlled conditions (26 ± 2 °C and 65 ± 5% RH).


The stock culture of the C. undecimpunctata started with adults that` were collected from aphid-infested tomato cultivars in Nobaryia, Egypt. Each of the 5 adults was kept in 2-L glass jars. The jars were supplied with fresh lettuce leaves infested with aphids for feeding. The jars were covered with muslin cloth held in position by rubber bands. Food was renewed every other day. The jars were checked daily for eggs. The eggs were collected and transferred to Petri dishes (20-cm diameter) till hatching. Neonate larvae were transferred individually to plastic cups with ample amount of Ephestia kuehniella Zeller (Lepidoptera: Pyralidae) eggs till reaching the proposed experimental stage ( second larval instar). Unused larvae were left in 2-L glass jars (5 each) with supply with small duranta branches carrying different stages of aphids for feeding till maturation.


Destruxin A-760 and Destruxin A-724 obtained from Shanghai Fuang Agrochemical Co. Ltd (99.9% purity) and prepared according to Guan et al. (2008). Six aqueous concentrations of both destruxins were prepared: 2.000, 1.000, 0.750, 0.500, 0.250, and 0.125 ppm. Fresh tomato leaves were dipped in each concentration for 10 s and left to dry at room temperature. Treated leaves were offered to third nymphal instars (20 nymphs/concentration). A parallel control of non-treated tomato leaves dipped in distilled water was run. Each treatment was replicated five times. The percentage of mortality was recorded after 7 days (Sabbour and Shaurub 2018) of treatment and corrected against that of the control according to the method described by Abbott’s formula (Abbott 1925). Corrected mortality was subjected to probit analysis (Finney 1971) to determine the LC50 value. All experiments were run under the aforementioned laboratory conditions.

Treatment of pests

Fresh tomato leaves were sprayed with the desired Destruxin A-760 and Destruxin A-724 concentration (3 shots as spurts/leaf ) ( Matter et al. 1993), left to dry and placed in 1-L plastic containers (one each). Then, 20 nymphs of M. persicae were placed on each leaf. Five containers (replicates) were used/concentration/microbial pathogen (destruxin)/aphid. Each container was covered with muslin and incubated at 25 °C, thereafter, untreated leaves were introduced in the plastic containers to allow the gentle transfer of survivors to them and the previously treated leaves were discarded. Untreated leaves were placed in plastic containers sprayed with water only and used as the control treatment. The experiment was replicated four times. The percentages of mortality were calculated after 7 days and corrected and treated as above.

Treatments of predator

One-day-old adults, second instar larvae of C. undecimpunctata, and second instar nymphs of M. persicae were used for evaluation of the pathogenicity and efficacy of Destruxin A-760 and Destruxin A-724. This was accomplished by different techniques.

A—Spray technique to evaluate the contact effect

B—Feeding technique to evaluate oral toxicity, either obligatory (no choice) (exposure to treated preys only) or free choice exposure to both infected and uninfected preys, and to investigate whether the predator has the ability to distinguish between the infected, uninfected preys, and not

Spray technique

Groups (20 predators of 1-day-old adults of C. undecimpunctata or 1-day-old second nymphal stage/group) were placed in a Petri dish (19-cm diameter) and sprayed with the fungus at 2.00 ppm concentration level using a small atomizer, by three shots as spurts (Matter et al. 1993). The shots were directed to the insects at a 15-cm distance, then the insects were individually transferred gently, using tweezers, to plastic cups (5-cm diameter and 12 cm) with small water moist filter paper and aphid-infested tomato leaf. The cups were covered with muslin and incubated at 25 ° C. The filter paper and branches carrying aphids were renewed every other day. Five groups (20 individuals/group) from each stage were used for each destruxin.

The cups of each group were checked daily for insects showing signs of fungus infection. The death toll was recorded for two weeks post-treatment and mortality percentages were calculated in each case.

Obligatory and free-choice feeding techniques

Groups of 20 individuals of either adults of C. undecimpunctata or second instar nymphs of M. persicae per group were exposed either obligatory to contaminated diet (pathogen-treated aphids) or selectively to pathogen-treated and untreated aphids for 24 h. In case of free-choice feeding, 5 groups were used/pathogen/predator stage. The predator was kept starved for 4 and 6 h for M. persicae, respectively, then, each group was introduced in the middle of a 5-L glass jar with 2 branches of tafla carrying ample amounts of the pest (one branch was previously sprayed with the destruxins while the other branch was sprayed with water only). The two branches were placed on both sides of the glass jar facing each other to allow the predator individuals free-choice to feed on either treated or untreated aphids. Five glass jars (replicates) were used for each pathogen.

Regarding obligatory feeding, the same number of predators in each of 5 glass jars were used as mentioned above but offered only treated aphids. In both trials, the exposure period was 24 h. Then predators of every treatment and the control as well were transferred individually to plastic cups, offered untreated aphids, and checked daily for 14 days

Field experiments


Experiments were carried out to study the efficacy of the tested two destruxins against the target insect pests in two different areas that differ in climatic and soil factors: in Ibn Malek (El-Nobaryia region) with dry weather and sandy soil and in El-SharKia (Zagazig) with wet weather and clay soil. Tomato (Var. Bio-Bride) was planted at the first of April in an area of about 1200 m2, divided into 12 plots of 100 m2each. Four plots were assigned for each pathogen, while 4 plots were treated with water and used as controls Destruxin A-760 and Destruxin A-724 were applied at 5 ppm concentration and 5 L/plot. Treatments were performed in a randomized plot design at the sunset with a 5-L sprayer. Three applications were made at 1-week intervals at the commencement of the experiment, then 20 samples of plants were randomly collected every week from each plot and transferred to the laboratory for examination. The average number of each of the tested pests/sample/plot/treatment was calculated 20, 50, 90, and 120 days post first application. The infestation of aphids was then determined in each case.

After harvest, the yield of each treatment was weighed as kg/F. Yield loss was calculated according to the following equation:

$$ \mathrm{Yield}\ \mathrm{loss}=\frac{\mathrm{potential}\ \mathrm{yield}-\mathrm{actual}\ \mathrm{yield}}{\mathrm{Potential}\ \mathrm{yield}}\times 100 $$

Potential yield was that of which gave the best results among the tested pathogens Destruxin A-760 and was taken as a base for comparison with the other treatments.


Seedlings of tomato plants were sown in rows (ca 50 cm apart) in ca 0.5 F located in the El Sharkia Governorate. One-month-old plants were found highly infested with M. persicae. The cultivated area was divided longitudinally into 3 areas (ca Kirat/each), separated from each other by uncultivated bare and had 4 m/width. One area was used for each entomopathogen toxin tested and the check as well. Each pathogen was sprayed at the rate of 5 ppm/F, using a high pressure hand held gun. The concentration of the Destruxin A-760 and Destruxin A-724 was about 5 ppm. (This concentration was previously achieved more than 80% mortality in both pests in laboratory experiments.) Three applications were made first at 1-week intervals. Then, count of C. undecimpunctata on nymphs and adults of M. presicae were carefully counted on site in all tomato plots visually, hand picking, and finally, sweeping net (25-cm diameter). The counts were made just before the first application and 1, 2, and 3 weeks post last application. The predators were placed again after each count on their previous location in the corresponding plant site. Fifty tomato shrubs (10 from each of 5 raws) per each treated area and the control as well were arbitrarily chosen/each time interval. The average number of predators/50 plants/time interval was calculated in each case. The increase or decrease in the population of the predator/50 plants as compared with the check was calculated according to Hendrson and Tilton’s (1955) equation as follows:

$$ \%\mathrm{increase}\ \mathrm{or}\ \mathrm{decrease}\ \mathrm{in}\ \mathrm{population}\ \mathrm{density}\kern0.5em =\kern0.5em \frac{\mathrm{Ca}}{\mathrm{Cb}}\kern0.5em \times \frac{\mathrm{Tb}}{\mathrm{Ta}}-1\times 100 $$

where Ca = population density in the treated area before treatment, Cb = population density in the treated area after treatment, Ta = population density in treated before treatment, and Tb = population density in the treated area after treatment.


Table 1 shows that the LC50 of M. persicae was 58 and 66 ppm when treated with Destruxin A-760 and Destruxin A-724, respectively.

Table 1 Effect of the destruxin tested against M. persicae under laboratory conditions

Under field conditions in both localities, M. persicae infection was significantly decreased. After 20 days of applications, the infections with the target pest obtained, 14 ± 4.7 and 11 ± 7.9 individuals in Destruxin A-724. Treated plots in Ibn Malek Nobaryia (Behira) and EL Sharkia (Zagazig), respectively. The corresponding data obtained 0 and 6 ± 1.2 individuals after Destruxin A-760. Treatment plots as compared to 56 ± 6.6 and 65 ± 8.9 individuals in the corresponding treatment areas.

In plots treated with Destruxin A-760, the infestations with M. persicae significantly decreased to 23 ± 4.5 and 36 ± 7 individuals, respectively, as compared to 152 ± 7.8 and 163 ± 4.7 individuals in the control, after 120 days of applications in both two governorates. The same obtained in case of Destruxin A-724 application after 120 days, the number of target insects were significantly decreased to 36 ± 7.7 and 46 ± 6.6 in Ibn Malek Nobaryia and EL Sharkia as compared to 152 ± 7.8 and 163 ± 4.7 individuals following the same order (Table 2).

Table 2 The infestation of tomato plants with M. persicae after treatment with Destruxin A-724 and Destruxin A-760 under field conditions

Effects of Destruxin A-760 and Destruxin A-724 on the predator on C. undecimpunctata were shown in Table 3, all of the experiment results cleared that the predator C. undecimpunctata was not affected to both destruxins treatments. This predator C. undecimpunctata proved a higher resistance against destruxin treatments Table 3. Our results show that the predator preys on nymphs which are more susceptible to that on the adult stages of C. undecimpunctata. Under laboratory conditions, the nymph’s mortality of M. persicae obtained 79.10 ± 7.61 and 21.2 ± 4.45 after treated with Destruxin A-760 and Destruxin A-724, respectively (Table 3). In case of adult stages, they significantly decreased by 0.6 times treated with the following in the same order.

Table 3 Determination of the effect of (Destruxin A-760 and Destruxin A-724) on developmental stages of C. undecimpunctata after feeding M. persicae nymphs and adults

In general, the indirect treatments by feeding by either of the treated of the prey M. persicae only (required) or by free-choice feeding on either treated or untreated prey (selectivity) revealed that the required ingestion of Destruxin A-760-infected prey of M. persicae caused a mortality percentage of 2.56 and 2.31 times that obtained from those of the given free-choice ingestion (selection treatment) for adult and nymph of C. undecimpunctata predators, respectively. The corresponding ratios for Destruxin A-724 were about 1.35 and 1.86, respectively. This indicated that the predator, particularly the adult predator, has a greater ability to recognize between the Destruxin A-760-treated prey and non-treated ones than Destruxin A-724fungus, which indicates that the adult predator can avoid Destruxin A-760 which infected the prey much more than that of the adult predator C. undecimpunctata avoiding the Destruxin A-724-infected prey. It is worth mentioning that no death from both destruxin’s infection was encountered in the check within the experimental period.

Under field conditions the experiments results showed that the population density of the predator C. undecimpunctata in the Destruxin A-760-treated area showed 36.22 and 19.81% reductions, 1 and 2 weeks after the last application, respectively. While the corresponding densities in the control area showed a 21.33 and 2.7% increase. However, the population, 3 weeks after the last application surpassed that of the check, showing a 6.36% increase (Table 4). In the I. fumosorosea-treated area, severe reductions in the population densities (63.33 and 43.99%) were estimated in the first and second weeks after the last application, respectively. There was less reduction (21.42%) estimated 3 weeks after the last application. However, the relatively higher reductions in predator densities in the treated areas, in the first weeks after the application. percentages increased or decreased in the C. undecimpunctata population as compared with the check according to Hendrson and Tilton (1955).

Table 4 The effect of destruxins on C. undecimpunctata (all stages)/50 tomato shrubs after successive post toxin application in tomatoes

Field application of both the two bio-insecticides showed that in the control plots, the estimated yield weights were 2169 ± 36.82 and 2000 ± 80.54 kg/F in Ebn-Malek Nobaryia (Behira) and EL Sharkia governorate (Zagazig) during the season of 2018, respectively. While in Destruxin A-760- and Destruxin A-724-treated plots, the estimated weights of the tomato yields were 3988 ± 34.31 and 3158 ± 42.57 kg/F, respectively, in the Ebn-Malek El-Nobaryia (Behira) region. In the El Sharkia (Zagazig), the untreated plots recorded 1990 ± 80.54 kg/F but the weight showed a significant increase post of the Destruxin A-760 and Destruxin A-724 treatments. The percentages of yield loss in the untreated plots were 30 and 33% in the Ebn-Malek El-Nobaryia (Behira) and the El Sharkia (Zagazig), respectively (Table 5).

Table 5 Weight of harvested tomatoes and percentage of yield loss during season 2018 post the two-destruxin treatments of M. persicae in two governorates


The present study showed that C. undecimpunctata exhibits relatively high and reasonable resistance to the tested entomopathogenic fungi Destruxin A-724 and Destruxin A-760 infections, respectively, even when exposed to a lethal concentration for the prey insects.

Thungrabeab and Tongma (2007) concluded that some genera of fungi could be specific and might inflict only on certain types of hosts. They reported the work of James and Lighthart (1994) who declared that the fungus N. rileyi exhibits host preferential infection in lepidopterous larvae. Also, they found that M. anisopliae, B. bassiana, and P. fumosorosea fungi have potential to infect Hippodomia converges (coccinellidae) whereas N. rileyi did not. Goettel et al. (1990) found that some commercial formulation of the entomopathogenic fungi can control aphids and thrips with low impact on non-target insects. Todorova et al. (1994) found that different strains of (B. bassiana) fungus showed different effects on the two Coleopterous predatory insects due to the host response of the insects. Sabbour and Sahab (2007) control Agrotis ipsilon and Heliothis armigera by the entomopathogenic fungi. Sabbour and Abdel-Rahman (2007) found that the two microbial control agents reduce the number of sugar beet pests under laboratory and field conditions. Sabbour (2007a, 2007b) found that the entomopathogenic fungi Nomuraea rileyi and Isaria fumosorosea proved highly pathogenic to aphids and the natural enemies Coccinella spp. were not affected by the fungi treatments. Poprawiski et al. (1998) found that Serangium parcestosrum (Coccinellidae) had lower survival potential when sprayed with Zagazig (B. bassiana) fungus than that with P. fumosorosea fungus. Shanthakumar et al. (2010) considered that in spite of the great virulence of N. rileyi against Spodoptera litura, the pathogen proved reasonable safety to Trichogramma chilonis. It did not cause a reduction in their parasitization percentages.

The present results also indicated that the predator, C. undecimpunctata, particularly adult predators can distinguish between fungus infected from non-infected preys and they almost avoid treated ones, especially if given free choice feeding. This, however, was more pronounced in the case of N. rileyi than P. fumosorosea. Such observed phenomenon in our investigations was viewed by many authors. It was mentioned that predators, when given free choice to feed upon fungus-treated or untreated aphids, predation on infected preys was less than uninfected ones (Baverstock et al. 2007). Also, Roy et al. (2010) and Goettel et al. (1990) proved that C. septempunctata adults avoid contacting with leaf and soil surface inoculated with B. bassiana fungus and mycosed cadavers. The predator was positioned away from mycosed cadaver than uninfected ones.

Nevertheless, some researches indicated several adverse effects of some entomopathogenic fungi against some natural enemies. It was considered that C. septempunctata was somewhat susceptible to B. bassiana (Haseeb and Murad 1997; Delete et al. 1995). Farag (2008) considers that some entomopathogenic formulations of B. bassiana have deleterious effects on C. undecimpunctata if applied at high-concentration levels. However, different views about the safety of entomopathogenic fungi, declared by many authors, might be due to the relative efficacy of the fungus or its isolates on pests the exhibit different susceptibilities, bionomics, and characters as well as types of assessment and application rates.


Destruxin A-760 and Destruxin A-724 are a promising control against M. persicae as they reduce the pest population under laboratory conditions. On the other hand, in the population under field conditions, the pathogen significantly reduced the target pests. Pathogen Destruxin A-760 and Destruxin A-724 tested non-significant effects on the predator’s populations.

Availability of data and materials

Not applicable for this section.


  1. Abbott WS (1925) A method of computing the effectiveness of an insecticide. J Econ Entomol. 18:265–267

    CAS  Article  Google Scholar 

  2. Baverstock J, Roy HE, Brown PM, Ware RL, Majerus MEE, Pell JK (2007) The invasive Coccinellid, Harmonia axyridis as an intra-guild predator of aphid specific fungus, Pandora neoaphidis. 40th Ann. Meeting of soc. For Invertbrate. Pathol., Quebic city, Canada 12-15 Aug 23.

  3. Berry RE (1998) Insects and mites of economic importance in the specific northwest, vol 221, 2nd edn. Osu Bookstore, Inc., Corvallis, OR, USA

    Google Scholar 

  4. Blackman RL, Eastop VF (2006) Aphids on the world’s herbaceous plants and shrubs. Volume 2 The aphids. John Wiley & Sons with the Natural History Museum, London viii + pages 1025-1439.

    Google Scholar 

  5. Delete KM, Grace JK, Tom CHM (1995) Potential use of pathogenic fungi in baits to control the Formosan subterranean termites (Isop: Rhinotewrmitidae) J. Appl Ent. 119(6):429–433

    Article  Google Scholar 

  6. Farag NA (2008) Impact of entomopathognic fungi on the aphid, Brevicoryne bressicae L. And its associated predator, Coccinella undecimpunctata L. Egyptian J Biol Pest Control 18(2):297–301

    Google Scholar 

  7. Filotos MG, Wraight SP, Sanderson JP (2004) Selection of entomopathogenic fungi for microbial contol of aphid pests in US greenhouses. Socity of Inverteb. Pathol. Proc. Annual Meeting, pp 37–97

    Google Scholar 

  8. Finney DJ (1971) Probit analysis, 2nd edn. Univ. Press. England, Cambridge

    Google Scholar 

  9. Goettel M, Poprawski TG, Vandenberg JD, Li Z, Roberts DW, (1990) Safety to nontarget invertebrates of fungal biocontrol agents. In Lord, M.; Lacey, LA. and Davidson EW. Eds. Safety of microbial insecticides. CRC Press PP. 209- 231.

  10. Guan H, Chi D, Yu J, Li X (2008) A novel photodegradable insecticide: preparation, characterization and properties evaluation of nano-Imidacloprid. Pestic Biochem Physiol. 92:83–91

    CAS  Article  Google Scholar 

  11. Haseeb M, Murad H (1997) Susceptibility of the predator Coccinella septempunctata to the entomopathogenic fungus Beauveria Bassiana. Ann Plant Prot Sci. 5(2):188–209

    Google Scholar 

  12. Hendrson CF, Tilton EW (1955) Test with acaricides against the brown wheat mite. J Econ Entomol. 48:157–161

    Article  Google Scholar 

  13. Howe GA, Jander G (2008) Plant immunity to insect herbivores. Annu Rev Plant Biol. 59:41–66

    CAS  Article  Google Scholar 

  14. James RR, Lighthart B (1994) Susceptibility of ladybeetle (Coleoptera, Coccinellidae) to four entomogenous fungi. Environ Ent. 23:190–192

    Article  Google Scholar 

  15. Matter MM, Marei SS, Moawad SM, El-Gengaihi S (1993) The reaction of Aphis gossypii and its predator, Coccinella undecimpunctata to some plant extracts. Bull Fac Agri Cairo. 44:413–432

    Google Scholar 

  16. Namba R, Sylvester ES (1981) Transimission of cauliflower mosaic viruses by the green peach. J Econ Entomol. 74:546–551

    Article  Google Scholar 

  17. Odier A F, Vey J P, Bureau, (1992) In vitro effect of fungal cyclodepsipeptides on leukemic cells: study of destruxins A, B and E. Biology of the cell 1992-1-1

    Google Scholar 

  18. Poprawiski TJ, Crisotomo LG, Parker P E, (1998) Influence of entomopathogenic fungi on Serangium parcesetosum ( Col. Coccinellidae) on important predator of whitefly ( Hom. Aleyrodidae Inviron Ent. 27: 785-795.

  19. Roberts DW (1981) Toxins of Entomopathogenic Fungi. Microbial control of pests and plant diseases. 1970-1980. Burges HD. Academic Press, New York 1981; 441-464.

  20. Roy HE, Freeman SN, Ormond EL, Thomas APM, Bell JK (2010) Coccinella septumpunctata avoids the generalist entomopathogenic fungus Beauveria bassiana. Int. Symp. Ecology of Aphidophaga perugia. Italy 11:19–24

    Google Scholar 

  21. Sabbour MM (2007a) Evaluations of some entomopathogenic fungi and the predator Coccinella septempunctata against cereal aphids in Egypt, 2007. Egypt Bull Ent Soc Egypt Econ. 33:165–174

    Google Scholar 

  22. Sabbour MM (2007b) Effect of some natural bioagents and natural enemies against aphids in wheat fields J. Boil Pest Cont 33:33–39

    Google Scholar 

  23. Sabbour MM, Abdel-Rahman A (2007) Evaluations of some terpenes and entomopathogenic fungi on three sugar beet insect pests. J Boil Pest Cont. 17:22–29

    Google Scholar 

  24. Sabbour MM, Sahab AF (2007) Efficacy of some microbial control agents against Agrotis ipsilon and Heliothis armigera in Egypt . Bull. N. R. C. Egypt.13

  25. Sabbour MM, Shaurub E-SH (2018) Evaluations of Metarhizium anisopliae and two Destruxin against cotton leaf worm Spodoptera littoralis (Lepidoptera: Noctuidae) under laboratory and field conditions. Bioscience Res 15(2):1028–1033

    Google Scholar 

  26. Shanthakumar SP, Murali PO, Malarvannan VP, Nair S (2010) Laboratory evaluation on the potential of entomopathogenic fungus Nomuraea rileyi against tobacco caterpillars and its safty to Trichogramma spp. J. biopesticides 3(1 special issue):132–137.

    Google Scholar 

  27. Thungrabeab M, Tongma S (2007) Effect of entomopathonic fungi, Beauveria bassiana and Metarhizium anisopliae on nontarget insects. J KMITL Sci Tech 7(51).

  28. Todorova SI, Cote JL, Martel P, Coderre D (1994) Hetrogenity of two Baeuveria bassiana strains on two coleopteran predators. Entomophoga 39:159–169

    Article  Google Scholar 

Download references


We acknowledge the National research center which supported this project.


This work was supported and funded by the National Research Centre through the project titled: Some strategies for improving weed control efficacy in some export crops. Project No. 11030139, during in-house projects strategy 2016–2019.

Author information




The author equally contributed in all the article parts. The author read and approved the final manuscript.

Authors’ information

Prof. Dr. Magda Sabbour is a profesor at the National Research Centre, Dokki, Giza, Pests and Plant Protection Department; Agricultural and Biological Division.,

Corresponding author

Correspondence to Magda Mahmoud Sabbour.

Ethics declarations

Ethics approval and consent to participate

Not applicable for this section.

Consent for publication

Not applicable for this section.

Competing interests

The author declares that she has no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Sabbour, M.M. Effect of destruxin on the population reduction of green peach aphid Myzus persicae (Hemiptera: Aphididae) and the predator Coccinella undecimpunctata (Coleoptera: Coccinellidae) in tomato fields. Bull Natl Res Cent 43, 132 (2019).

Download citation


  • Destruxin A-760
  • Destruxin A-724
  • My z us persicae
  • Coccinella undecimpunctata
  • Egypt
  • Tomato pests
  • Entomopathogenic fungi toxin