www.eajbs.eg.net Virulence of Entomopathogenic Nematodes Steinernema glaseri and Heterorhabditis bacteriophora Poinar (HP 88 strain) Against the Black Cutworm, Agrotis ipsilon.

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a b s t r a c tNowadays, finding a safe control program is the aim of all researchers. The goal of this work is to investigate the effect of gamma radiation on the Entomopathogenic nematodes, Steinernema scapterisci and Heterorhabditis bacteriophora Poinar (HP 88 ) efficacy were tested against larvae of cotton leaf worm, Spodoptera littoralis (Boisd.) under laboratory conditions. Results showed that 2 Gy irradiated S. scapterisci and H. bacteriophora were substantially effective in controlling S. littoralis larvae, while H. bacteriophora was more potent in controlling insect larvae. The results revealed that total protein concentration was significantly decreased (P < 0.05) after treatment with normal or irradiated H. bacteriophora or S. scapterisci. In addition, larvae infected with normal S. scapterisci or H. bacteriophora showed a significant elevation in phenoloxidase activity and represented significant reduce after treatment with 2 Gy irradiated S. scapterisci or H. bacteriophora as compared to control group. Also, lysozyme activity was significantly decreased after treatment with irradiated H. bacteriophora, but there was no significance with irradiated S. scapterisci, when compared with control. LDH activity was significantly high (p<0.05) in the haemolymph of larvae treated with normal or irradiated H. bacteriophora or S. scapterisci, as compared to control group. Furthermore among all treatments, 2 Gy irradiated H. bacteriophora was the most potent and efficient in the biomarkers changes. Therefore, it could be concluded that 2 Gy irradiated S. scapterisci and H. bacteriophora can serve within an integrated pest management (IPM) program in an agroecosystem.

(1) Background: Citrus honey constitutes a unique monofloral honey characterized by a distinctive aroma and unique taste. The non-targeted chemical analysis can provide pivotal information on chemical markers that differentiate honey based on its geographical and botanical origin. (2) Methods: Within the PRIMA project “PLANT-B”, a metabolomics workflow was established to unveil potential chemical markers of orange blossom honey produced in case study areas of Egypt, Italy, and Greece. In some of these areas, aromatic medicinal plants were cultivated to enhance biodiversity and attract pollinators. The non-targeted chemical analysis and metabolomics were conducted using ultra-high-performance liquid chromatography high-resolution mass spectrometry (UHPLC-HRMS). (3) Results: Forty compounds were disclosed as potential chemical markers, enabling the differentiation of the three orange blossom honeys according to geographical origin. Italian honey showed a preponderance of flavonoids, while in Greek honey, terpenoids and iridoids were more abundant than flavonoids, except for hesperidin. In Egyptian honey, suberic acid and a fatty acid ester derivative emerged as chemical markers. New, for honey, furan derivatives were identified using GC-MS in Greek samples. (4) Conclusions: The application of UHPLC-HRMS metabolomics combined with an elaborate melissopalynological analysis managed to unveil several potential markers of Mediterranean citrus honey potentially associated with citrus crop varieties and the local indigenous flora.

The present work mainly focused on the susceptibility of Schistocerca gregaria (Forskal(5 th instar nymphs to the entomopathogenic nematodes, Steinernema glaseri (Rhabditida: Steinernematidae) as a natural exposure experiment. The entomopathogenic nematode, S. glaseri turned out to be successful parasitoid of the orthopteran insect S. gregaria. The death rate of locusts (sprayed with nematode on clover leafs) was remarkably high. Nematode killed approximately 65% of the locust with in 72 hours post infection at semi-field trial. The impact of parasitation on locusts' immune defense was closely investigated for S. gregaria parasitized by S. glaseri. Nymphs died within 48-72h after being fed clover leafs contaminated with 1500/ml S. glaseri juveniles or previously contaminated with the dual cyclooxygenase/lipoxygenase inhibitor, phenidone. The injection of S. gregaria nymphs with, phenidone exhibited significant reduction in microaggegation in response to the nematode injections. At 12h post-injection, insignificant differences were recorded of the individual inhibitor on microaggregation, compared to the ethanol-treated (control) nymphs. Cellular defense components were strongly influenced by parasitation within the first 12h after injection of the nematodes. Nymph's haemolymph was assayed.