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Assessment of the entomopathogenic nematodes against maggots and pupae of the oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae), under laboratory conditions


The oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) is one of the major insect pests which renders the fruit to become unfit for human consumption. In severe cases, losses may reach up to 100% in some fruit crops. The present study aimed to investigate the pathogenicity of entomopathogenic nematodes (EPNs), Heterorhabditis bacteriophora, H. indica, Steinernema carpocapsae, and S. asiaticum against B. dorsalis maggots and pupae under laboratory conditions. One milliliter of EPNs, having 50, 75, and 100 infective juveniles (IJs) against maggots and 100, 150, and 200 IJs against pupae, were poured into 9 cm Petri dishes with 20 g sterilized soil as supporting media. The highest maggots’ mortality (70%) was obtained after 3 days of application of H. bacteriophora and S. carpocapsae and reached up to (96%) after 9 days. S. asiaticum and H. indica caused 91.16 and 85.87% mortality, respectively, after 9 days post treatment at the highest nematode concentration (100 IJs/ml). Whereas, against the fruit fly pupae, H. bacteriophora caused 69.08% mortality after 9 days at the highest concentration (200 IJs/ml). All nematode species showed high effectiveness against both stages of B. dorsalis. Their application can be further evaluated under field conditions to promote a good biological control of fruit flies for healthier fruit production.


Pakistan is ranked tenth among citrus producing countries in the world for citrus production (Mahmood and Sheikh 2006). Above 90% of the citrus fruits are produced in the Punjab province and are distributed through different value chains to domestic as well as international markets (GOP (Government of Pakistan) 2012). Citrus fruits are infested, from fruit setting to ripening and harvesting, by a number of insect pests and diseases but the fruit flies are the major destructive pests, which cause substantial yield losses. Fruit flies not only attack citrus but also attack a variety of fleshy fruits and vegetables in tropical and subtropical areas of the world (Roger et al. 2015). Among the fruit fly species, the oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) is an important insect pest of citrus fruits. Application of chemical insecticides has been the main tool of citrus growers to control this voracious insect pest, which not only leads towards the development of insecticidal resistance but also pose serious threats to the environment and human health. Application of entomopathogenic nematodes (EPNs) can be good alternatives to the conventional chemical insecticides as they have biological mode of action and resistance is unlikely to develop against these agents. The infective juveniles of the nematode enter the host body through body openings and release the associated bacterium, which multiply and deplete the host nutrients and ultimately kill it (Griffin et al. 2005).

EPNs have been used by different scientists in different countries for the management of various pests and have shown efficient results. In 2014, Nouh and Hussein used EPNs as bio-control agents against Ceratitis capitata (Wied.) and Bactrocera zonata (Saund.) in Egypt. Similarly, EPN, Steinernema feltiae, significantly decreased the larval population of Leptinotarsa decemlineata under field conditions (Laznik et al. 2010), while after the application of the same EPN, the damage to the leaves caused by Frankliniella occidentalis was reduced in greenhouse by lowering the pest population (Trdan et al. 2007).

The present study aimed to investigate the pathogenicity of Heterorhabditis bacteriophora, H. indica, Steinernema carpocapsae, and S. asiaticum against B. dorsalis larvae and pupae under laboratory conditions.

Materials and methods

Sampling and rearing of Bactrocera dorsalis

B. dorsalis maggots-infested fruits, collected from the local fruit market, were brought to the Integrated Pest Management (IPM) Laboratory, College of Agriculture, Bahauddin Zakariya University (BZU), Bahadur Sub-Campus, Layyah, Pakistan, and were kept in plastic cages containing sterilized sand at 25 ± 1 °C and 65%RH. The full-grown maggots hopped from the fruits and pupated in the sand. Adult flies were fed with 20% honey solution in hanging inside cups containing fresh ripen fruits for egg-laying. After egg-laying, the fresh fruits were shifted to new rearing cages to get next progeny to be used in the experiments. The infested fruits were dissected to get the maggots for experiments.

Entomopathogenic nematodes

Infective juveniles (IJs) of S. asiaticum, S. carpocapsae, H. bacteriophora, and H. indica were obtained from Nematology Laboratory, Department of Plant Pathology, University of Agriculture, Faisalabad, Pakistan. The EPNs were cultured on Galleria mellonella L. larvae (Lepidoptera: Pyralidae) following the procedures of Woodring and Kaya (1988).

Maggots’ bioassay

To investigate the infectivity of EPNs, 3 different concentrations; 50, 75, and 100 IJs/ml−1 of all EPN species were prepared in glass jars. One milliliter of each EPN species was poured into 9 cm Petri dishes containing 20 g sterilized soil (40% sand, 40% silt, and 20% clay) as supporting media (Heve et al. 2017). Twelve maggots of B. dorsalis of uniform size and age (third instar) were released into each dish and wrapped with parafilm. Petri dishes, treated with distilled water only, served as control. The experimental conditions were maintained at 25 ± 2 °C, 75 ± 5% RH, and 12:12 (D:L) hour photoperiod in an incubator (Minas et al. 2016 and Raheel et al., 2017). Mortality data were recorded on third, sixth, and ninth day post exposure to EPNs. All the treatments were repeated five times.

Pupal bioassay

For pupal bioassay, the same procedure was used but the nematode concentrations were 100, 150, and 200 IJs/ml. Twelve, 1-day-old pupae were introduced in each Petri dish. The data for adult emergence was recorded on a daily basis for 10 days.

Statistical analysis

Mortality rates were corrected for control treatment mortality using Abbott’s (1925) formula. The mortality and adult emergence data were subjected to analysis of variance (ANOVA), using Minitab 17 software (Minitab 17, 2010) and the means were separated by Tukey’s Kramer test (HSD) (Sokal and Rohlf, 1995) at 5% significance level.

Results and discussion

Maggots’ bioassay

B. dorsalis maggots were significantly susceptible to all the tested EPN species at all concentrations applied as compared to the control. S. carpocapsae caused the highest mean mortality rates at all concentrations (Table 1). At the concentration of 100 IJs/ml, S. carpocapsae caused 71.12, 93.20, and 96.46% mortality in maggots after 3, 6, and 9 days of application, respectively. The lowest mortality rate was achieved by the H. indica; 37.15, 72.82, and 85.87%, respectively, at the same concentration.

Table 1 Corrected percent mortality (mean ± SE) in Bactrocera dorsalis maggots (third instar) treated with Heterorhabditis bacteriophora, H. indica, Steinernema carpocapsae, and S. asiaticum at different concentrations and time period

The LC50 for S. carpocapsae was 30.2 IJs/μl, while it was 41.88 IJs/μl for H. bacteriophora, 46.99 IJs/μl for H. indica and 48.08 IJs/μl for S. asiaticum (Table 2). Similarly, the LC90 of S. carpocapsae was also the lowest (67.88 IJs/μl) than all other tested EPNs, but the highest LC90 was recorded for H. indica (110.5 IJs/μl) (Table 2). Gazit et al. (2000) assessed 12 different species of EPNs against pre-pupae of C. capitata, from which S. riobrave, Texas isolate, was the most infective. The authors concluded that the activity of IJs was correlated with EPNs species as well as concentration rate. Lindegren and Vail (1986) recorded 92% mortality rate when they applied the concentration of 5000 IJs/insect and only 9% mortality rate after application with 50 IJs/insect. Similar results were obtained by other researchers against different insect species (Laborda et al. 2003; Almeida et al. 2007; Malan et al. 2011 and Rohde et al. 2012). Similarly, S. carpocapsae and S. feltiae were found to be the most efficacious species under laboratory, semi-field, and field conditions with larval mortality of 88, 78, and 88%, respectively, of European cherry fruit fly, while no mortality of pupae was observed (Köppler et al. 2003). Stark and Lacey (1999) reported that the highest infection rate was caused by S. carpocapsae (65%), H. bacteriophora (50%), S. feltiae (35%), and H. marelatus (15%) against Rhagoletis indifferens larvae. Karagoz et al. (2009) confirmed the effectiveness of five local EPN species against last-instar larvae of C. capitata under controlled conditions. Sirjani et al. (2009) stated that S. feltiae was highly virulent against third instar larvae of Bactrocera oleae (G.) compared to S. carpocapsae, S. riobrave, S. glaseri, H. bacteriophora, and H. marelatus.

Table 2 Lethal concentrations (LC50 and LC90) of the tested EPNs against Bactrocera dorsalis maggots

Pupal bioassay

All the tested EPN species showed a high efficacy on the treated pupae at the highest concentrations, while at low concentrations caused the lowest mortality (Fig. 1). H. bacteriophora was superior and caused the highest mortality rates at all concentrations. The fruit fly pupae might be resistant to EPN penetration (Malan and Manrakhan, 2009). Many tested EPNs were found to have no ability to cause infection to pupal stage of different species of fruit flies (Lindegren and Vail, 1986; Yee and Lacey, 2003; Soliman, 2007 and Karagoz et al. 2009). Efficacy of H. baujardi LPP7 was evaluated against the fruit fly pupae by Minas et al. (2016) and recorded more than 80% mortality rate after application of 816 IJs/cm2. Most fruit fly larvae come out from the fruit for pupation in the soil at depth of few centimeters. This is a good habitat for the IJs to search and locate the target hosts and initiate infection (Stark and Lacey, 1999 and Sirjani et al. 2009). Kepenekci and Susurluk (2006) evaluated two Turkish strains of S. feltiae (All and S3) on pupae of Medfly and detected a low death rate after application of both strains, All (26.6% and 33.3%) and S3 (30% and 40%) after application of 50 IJs/ and 100 IJs/pupae, respectively. The low mortality rate of 1-day-old pupae could be due to cuticle hardness, which mainly reduces the penetration of the IJs. Minas et al. (2016) observed that mouth, spiracles, and anus, were quite open for penetration into pupae. However, the pupae of Anastrepha fraterculus were found to be vulnerable to infection by some EPN species, as it was highly susceptible to infection by S. riobrave and H. bacteriophora (Barbosa-Negrisoli et al. 2009). Similarly, Patterson Stark and Lacey (1999) gained high mortality rates (62.5 and 40%) of Rhagoletis indifferens pupae after application of H. bacteriophora and S. riobrave, respectively, but S. feltiae, S. carpocapsae, H. bacteriophora, and H. megidis effectively controlled all the life stages of L. decemlineata. The effectiveness of EPNs may vary depending upon the target species, life stage, and condition of the application (Trdan et al. 2007).

Fig. 1

Corrected percent mortality (mean ± SE) in Bactrocera dorsalis pupae after 10 days of treatment with Heterorhabditis bacteriophora, H. indica, Steinernema carpocapsae, and S. asiaticum at different concentrations


Results proved that EPNs are a promising tool to effectively reduce the populations of B. dorsalis larval stage. EPNs can be regularly used within an IPM plan to control the fruit fly pests under semi- and field conditions.

Availability of data and materials

All data of the study have been presented in the manuscript, and high quality and grade materials were used in this study.



Analysis of variance


Entomopathogenic nematodes


Infective juveniles


Integrated pest management


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

    CAS  Article  Google Scholar 

  2. Almeida JEM, Batista FA, Oliveira FC, Raga A (2007) Pathogenicity of the entomopathogenic fungi and nematode on medfly, Ceratitis capitata (Wied.) (Diptera: Tephritidae). Bioassay 2:1–7

    Google Scholar 

  3. Barbosa-Negrisoli CRC, Garcia MS, Dolinski C, Negrisoli JR, Bernardi D, Nava DE (2009) Efficacy of indigenous entomopathogenic nematodes (Rhabditidae: Heterorhabditidae, Steinernematidae), from Rio Grande do Sul Brazil, against Anastrepha fraterculus Wied (Diptera: Tephritidae) in peach orchards. J Invertebr Pathol 102:6–13

    Article  Google Scholar 

  4. Gazit Y, Rossler Y, Glazer I (2000) Evaluation of entomopathogenic nematodes for the control of Mediterranean fruit fly (Diptera: Tephritidae). Bio Sci Tech 10:157–164

    Article  Google Scholar 

  5. GOP (Government of Pakistan) (2012) Pakistan Economic Survey, Ministry of Finance. Economic Advisor’s Wing, Islamabad

    Google Scholar 

  6. Griffin CT, Boemare NE, Lewis EE (2005) Biology and behaviour. In: Grewal PS, Ehlers RU, Shapiro-Ilan DI (eds) Nematodes as biocontrol agents, 1st edn. CABI Publishing, Wallingford, pp 47–59

    Chapter  Google Scholar 

  7. Heve WK, El-Borai FE, Carrillo D, Duncan LW (2017) Increasing entomopathogenic nematode biodiversity reduces efficacy against the Caribbean fruit fly Anastrepha suspensa: interaction with the parasitoid Diachasmimorpha longicaudata. J Pest Sci 91(2):799–813

    Article  Google Scholar 

  8. Karagoz M, Gulcu B, Hazir C, Kaya HK, Hazir S (2009) Biological control potential of Turkish entomopathogenic nematodes against the Mediterranean fruit fly, Ceratitis capitata (Diptera: Tephritidae). Phytoparasitica 37:153–159

    Article  Google Scholar 

  9. Kepenekci I, Susurluk A (2006) Infectivity of two Turkish isolates of Steinernema feltiae (Rhabditida: Steinernematidae) against Rhagoletis cerasi and Ceratitis capitata. Nemato Medit 34:95–97

    Google Scholar 

  10. Köppler K, Peters A, Vogt H (2003) Initial results in the application of entomopathogenic nematodes against the European cherry fruit fly Rhagoletis cerasi L. (Diptera: Tephritidae). IOBC/ WPRS Bullet 23:13–18

    Google Scholar 

  11. Laborda R, Bargues L, Navarro C, Barajas O, Arroyo M, Garcia EM, Montoro E, Llopis E, Martinez A, Sayagues JM (2003) Susceptibility of the Mediterranean fruit fly (Ceratitis capitata) to entomopathogenic nematode Steinernema spp. (biorend C). Bulletin OILB/ SROP 26(6):95–97

    Google Scholar 

  12. Laznik Ž, Tóth T, Lakatos T, Vidrih M, Trdan S (2010) Control of the Colorado potato beetle (Leptinotarsa decemlineata [Say]) on potato under field conditions: a comparison of the efficacy of foliar application of two strains of Steinernema feltiae (Filipjev) and spraying with thiametoxam. J Plant Dis Prot 117(3):129–135

    CAS  Article  Google Scholar 

  13. Lindegren JE, Vail PV (1986) Susceptibility of Mediterranean fruit fly, melon fly and oriental fruit fly (Diptera: Tephritidae) to the entomogenous nematode Steinernema feltiae in laboratory tests. Environ Entomol 15:465–468

    Article  Google Scholar 

  14. Mahmood MA, Sheikh AD (2006) Citrus export system in Pakistan. J Agric Res 44(3):229–238

    Google Scholar 

  15. Malan AP, Knoetze R, Moore SD (2011) Isolation and identification of entomopathogenic nematodes from citrus orchards in South Africa and their biocontrol potential against false codling moth. J Invert Pathol 108:115–125

    Article  Google Scholar 

  16. Malan AP, Manrakhan A (2009) Susceptibility of the Mediterranean fruit fly (Ceratitis capitata) and the Natal fruit fly (Ceratitis rosa) to entomopathogenic nematodes. J Invertebr Pathol 100:47–49

    Article  Google Scholar 

  17. Minas RS, Souza RM, Dolinski C, Carvalho RS, Burla RS (2016) Potential of entomopathogenic nematodes (Rhabditida: Heterorhabditidae) to control Mediterranean fruit fly (Diptera: Tephritidae) soil stages. Nematoda 3:e02016

    Article  Google Scholar 

  18. Minitab 17 (2010) Statistical software. Minitab, Inc, State College.

    Google Scholar 

  19. Nouh GM, Hussein MA (2014) The role of entomopathogenic nematodes as biocontrol agents against some tephritid flies. Adv in Biol Res 8(6):301–306

    Google Scholar 

  20. Patterson Stark JE, Lacey LA (1999) Susceptibility of western cherry fruit fly (Diptera: Tephritidae) to five species of entomopathogenic nematodes in laboratory studies. J Invertebr Pathol 74(2):206–208

    CAS  Article  Google Scholar 

  21. Raheel M, Javed N, Khan SA, Aatif HM, Sohail A (2017) Effect of temperature on the reproductive potential of indigenous and exotic species of entomopathogenic nematodes inside Galleria mellonella L. larvae. Pak J Zool 49(1):419–421

    Article  Google Scholar 

  22. Roger IV, Pinero JC, Leblanc L (2015) An overview of pest species of bactrocera fruit flies (diptera: tephritidae) and the integration of bio pesticides with other biological approaches for their management with a focus on the Pacific region. J Insects 6:297–318

    Article  Google Scholar 

  23. Rohde C, Moino AJ, Carvalho FD, Silva MAT (2012) Selection of entomopathogenic nematodes for the control of the fruit fly Ceratitis capitata (Diptera: Tephritidae). Rev Bras Ciênc Agrár 7:797–802

    Google Scholar 

  24. Sirjani FO, Lewis EE, Kaya HK (2009) Evaluation of entomopathogenic nematodes against the olive fruit fly, Bactrocera oleae (Diptera: Tephritidae). Bio Con 48:274–280

    Article  Google Scholar 

  25. Sokal RR, Rohlf FJ (1995) Biometry: the principles and practice of statistics in biological research, 3rd edn. W.H. Freeman and Co, New York

    Google Scholar 

  26. Soliman NA (2007) Pathogenicity of three entomopathogenic nematodes to the peach fruit fly, Bacterocera zonata (Saunders) and the Mediterranean fruit fly, Ceratitis capitata (Wiedemann) (Diptera: Tephritidae). Egypt J Biol Pest Cont 17:121–124

    Google Scholar 

  27. Stark JEP, Lacey LA (1999) Susceptibility of Western fruit fly (Diptera: Tephritidae) to five species of entomopathogenic nematodes in laboratory studies. J Invertebr Pathol 74:206–208

    Article  Google Scholar 

  28. Trdan S, Žnidaračič D, Vidrih M (2007) Control of Frankliniella occidentalis on greenhouse-grown cucumbers: an efficacy comparison of foliar application of Steinernema feltiae and spraying with abamectin. Russ J Nematol 15(1):25–34

    Google Scholar 

  29. Woodring JL, Kaya HK (1988) Sternematidae and Heterorhabditidae nematodes: a handbook of techniques southern cooperative. Arkansas Agricultural Experimental Station Falleteville, Arkansas, p 88 Series Bulletin, 331

    Google Scholar 

  30. Yee W, Lacey LA (2003) Stage-specific mortality of Rhagoletis indifferens (Diptera: Tephritidae) exposed to three species of Steinernema nematodes. Bio Con 27:349–335

    Article  Google Scholar 

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The authors are grateful to lab technicians for assisting to carry out the study.


The study was conducted with the available laboratory resources without any aid from any funding agency.

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The authors carried out all the experiments, including the bioassay tests, analytical part, analysis of data, and wrote the manuscript. All authors read and approved the final manuscript.

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Correspondence to Sajjad Ali.

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Aatif, H.M., Hanif, M.S., Ferhan, M. et al. Assessment of the entomopathogenic nematodes against maggots and pupae of the oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae), under laboratory conditions. Egypt J Biol Pest Control 29, 51 (2019).

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  • Fruit fly
  • Bactrocera dorsalis
  • EPN
  • IJs
  • Biological control