Virulence of four entomopathogenic nematode against different stages of the Mediterranean fruit fly,

Background: Ceratitis capitata Wiedemann (Diptera: Tephritidae) (Mediterranean fruit fly), is one of the important polyphagous pest species in the world that harms almost all fruits causing significant yields losses. Control of this pest which is on the quarantine list of many countries is highly important. Due to the negative effects of chemical control on the environment and human health, biological control approaches have gained importance. Entomopathogenic nematodes (EPNs) are a potential biological control agent that can be used for effectively controlling the Medfly. Results: In this study, effects of four EPNs species on larvae, pupae and adults of Medfly were investigated under laboratory conditions. Four different concentrations of EPNs species were used against each stage of the pest. It pest showed different sensitivity to different concentrations of each of the tested EPNs. High mortality rate of 94% was caused by Heterorhabditis bacteriophora (11 KG),, followed by H. bacteriophora (TOK-20) with 91%, Steinernema carpocapsae (85%) and S. feltiae (Tokat-Emir) with 71% at highest concentration (200 IJ/larvae. The highest effect on adult mortality (100%) was recorded by the species S. feltiae (Tokat-Emir) at the highest concentration (200 IJ/adult) in the trials, followed by H. bacteriophora (11 KG) with 92%, H. bacteriophora (TOK-20) with 91% and S. carpocapsae (TokatBakışlı05) with 87.37% mortality rates at the same concentrations. Conclusions: It was determined that the EPNs tested in this study had insecticidal properties and they might be used in biological control programs against the Medfly.


Background
The Mediterranean fruit fly, Ceratitis capitata Wiedemann (Diptera: Tephritidae) is one of the economic polyphagous pest species in the world (Zucchi 2001). It has been recorded in 350 hosts from 65 different families around the world. especially to temperate climate fruits and subtropical fruits, some vegetables and ornamental plants worldwide (Weems 1981;Liquido et al. 1990Liquido et al. , 1991Woods et al. 2005;Thomas et al. 2010). Its damages to the exported products is very important for the country's economy as this causes economic losses by affecting the yield quantity and quality (Başpınar et al. 2009). Recently, researchers are seeking for alternatives pest control tools like biological control agents. Entomopathogenic nematodes (EPNs) are obligate insect pathogens found in soil that are used as biological agents. They have a wide host range, able to kill their hosts with the help of their symbiotic bacteria within 24-48 h, easy to mass produce, able to actively search and find their hosts, can stay alive for a long time in the absence of hosts, and do not harm the environment and humans. Studies of isolating EPNs and Yağcı et al. Egypt J Biol Pest Control (2021) 31:126 investigating their virulences have increased, and are of great importance for biological control studies (Hazır et al. 2003). Although the potentials of EPNs against many pest groups in the world have been demonstrated in laboratory and field / garden studies, there are few studies on fruit pests.

Mass rearing of Galleria mellonella larvae
Galleria mellonella's larvae were reared on a artificial diet, contained 890 g flour, 222 g dry baker's yeast, 500 g glycerin, 500 g honey, 445 g milk powder and 125 g beewax in an incubator with 16/8 h lighting set at 24-25 °C (Mohamed and Coppel 1983).

Mass rearing of entomopathogenic nematode species
Ten last instar G. mellonella larvae were placed in small Petri dishes with lined Whatman paper. A suspension EPNs of infective juveniles inoculated the larvae. Petri dishes were placed in an incubator at 20-23 °C. Dead larvae was controlled frequently. Infective EPNs juveniles were obtained from infected G. mellonella larvae, using the "White trap" method (White 1927). Juveniles were kept in a refrigerator at + 10 °C.

Rearing of the Medfly
The stock culture of the Medfly, reared in the Entomology Laboratory, was used in the experiments. Fruit fly production was carried out in plexiglass adult cages with 50 mesh tulle on both sides in climate rooms with 25 ± 1 °C, 65 ± 5% relative humidity, and 16 h light and 8 h dark conditions. Eggs laid by mature individuals were left on large Petri dishes on artificial media made from a mixture of bran, wheat germ, yeast, hydrochloric acid and water. The last instar larvae were collected 6-8 days after the eggs laying to be used in the experiments.

Experiments
Experiments were conducted using 150 ml plastic containers, containing the last instar larvae and pupae of the pest on soil mixture (80% sand, 15% soil and 5% clay) sterilized at 121 °C (Chen et al. 1995). Five-to 7-day-old pupae were used in the experiments. In adult trials, EPNs were applied by placing Whatman paper on the bottom of 150 ml plastic containers and a piece of cotton soaked in sugar melted water was also left in each container. Four concentrations (0, 50, 100, 200 IJs/C. capitata stages) for each nematode species were tested against both late instar larvae, pupae and adults of C. capitata. Trials had 10 replications of each concentration and 5 individuals per repeat (50 individuals in total). After placing the 5 individuals of the pest in each plastic container, the nematodes were applied by a pipette. Only distilled water and sugar melted water were provide as food for the adults in control group. All the trials were repeated twice, on different dates, and the set up was incubated at 25 °C under 16 h dark and 8 h light climatic room conditions. Mortality rates of adults and larvae were calculated 5 days after the inoculation, while pupae were calculated 10 days later. Dead medfly larvae, pupae and adults were collected and placed in the White trap method. About one week later, EPNs emerged from insect cadavers and were examined under a stereomicroscope.

Statistical analyses
In experiments, all data were analyzed by statistical program JMP 7. Analyses were done using one-way ANOVA and used "LSMeans Student's t test" for finding the variety in the effects of different nematode species and concentrations on Medfly.

Results
Data were evaluated 5 days after EPNs inoculation of the medfly's larvae and adults. Pupal data were evaluated after 10 days. Statistically, both parameters (species and concentrations) were found to be significant. Mortality rates of the last instar larvae of the medfly increased directly as the concentration increased in case of all EPNs species (p < 0.001).

Virulence of EPN species at different concentrations against Ceratitis capitata last instar larvae
It was observed that all the applications against the Medfly last instar larvae were quite effective than the controls. High mortality rates of all EPNs species against the last instar larvae of the Medfly were recorded at 200 IJs/ larva (at high concentration). High mortality rate (94%) was reported in case of H. bacteriophora (11 KG) isolate, followed by H. bacteriophora (TOK-20) with (91%), S.

Virulence of EPN species at different concentrations against pupae of C. capitata
The pupae were evaluated at 10 days after from the application. While the difference between the concentrations was significant, the difference between the species was not statistically significant. In pupal stage trials, applications were found to be effective than the control. The highest mortality rate was found at 200 IJs/pupa concetrations for all EPNs nemetode species.

Virulence of EPN species at different concentrations against adults of Ceratitis capitata
In all trials and concentrations against adults of the pest were found to be more effective than controls. In addition, as the concentration increased in all EPNs species used and the mortality rate of the adult individuals increased in direct proportion (p < 0.001). The highest mortality rate (100%) detected at 200 IJs/ adult concentration against the adults, was caused by S. feltiae (Tokat-Emir), followed by H. bacteriophora  (Table 3).   et al. Egypt J Biol Pest Control (2021) 31:126 Discussion C. capitata is a highly invasive species. It has a high dispersive ability, a very large host range. It has a high economic impact, affecting production, control costs and market access. (Malacrida et al. 2007). Several studies have been carried out to evaluate the efficiency of steinernematid and heterorhabditid nematodes against C. capitata. Karagöz et al. (2009)  Heterorhabditis sp. IS-5 (H IS-5) showed high activity and induced > 80% mortality. Six EPN strains showed limited activity (> 30% mortality), and 4 strains had no effect (< 20% mortality). Soliman et al. (2014) reported that the ability of H. bacteriophora infective juveniles to infect last insar larvae of B. zonata and C. capitata was more than S. riobrave.

Conclusions
Four EPNs species were found very effective against the C. capitata last instar larvae and adults. S. feltiae (Tokat-Emir) provided to be the best candidate among the other EPN species to control Medfly larvae, while H. bacteriophora (11 KG) was the best among the other EPN species to control the adults. However, the 4 isolates could all be used for the control of C. capitata biological control program in orchards. However, more field studies are needed to be conducted.