Galleria mellonella is used as a model organism to study the innate immune response of insects. In this study, the humoral immune response was assessed by examining phenoloxidase activity, fungal burden, and the expression of phenoloxidase and antimicrobial peptide genes at different time point following separate and combined injections of Hypericum perforatum extract and a nonlethal dose of Candida albicans. The administration of a plant extract at low doses increased phenoloxidase activity, while higher doses had no effect. Similarly, co‐injection of a low dose of the extract with the pathogen allowed half of the yeast cells to survive after 24 h. Co‐injection of plant extract with the pathogen decreased the phenoloxidase activity at the end of 4 h compared to C. albicans mono‐injection. The phenoloxidase gene expressions was reduced in all experimental conditions with respect to the control. When plant extracts and the pathogen were administered together, gallerimycin and hemolin gene expressions were considerably higher compared to mono‐injections of plant extracts and the pathogen. The results of this study reveal that gene activation and regulatory mechanisms may change for each immune gene, and that recognition and signaling pathways may differ depending on the involved immunoregulator.

Greater plantain (Plantago major), a medicinal plant species, is used in folk medicine for the treatment of various diseases in many countries of the world. Different studies have shown that the bioactive components contained in the plant have a dual effect. It was also reported that in vivo and in vitro studies showed different results. The aim of the study was to determine the effects of P. major extract on the hemocyte-mediated and humoral immune responses of the invertebrate model organism Galleria mellonella, which is widely used in immune studies. In the evaluation of these effects, total hemocyte count, encapsulation, melanization, phenoloxidase, superoxide dismutase, catalase, malondialdehyde and total protein parameters were evaluated. The results of the study showed that the total hemocyte count did not change, that the encapsulation responses decreased, that the melanization responses and phenoloxidase activity increased and that the superoxide dismutase activity decreased. As a result, it was determined that high doses of P. major had negative effects on cell-mediated immunity and antioxidant defence and positive effects on melanization. High doses and continuous use of P. major may have negative effects on living things.

Endoparasitoid species devoid of symbiotic viruses inject secretions derived from their reproductive glands into their hosts during parasitism in order to avoid various immune responses of their hosts. Pimpla turionellae L. (Hymenoptera: Ichneumonidae) is an endoparasitoid that lacks polydnaviruses, and its venom has previously been shown to paralyze the host Galleria mellonella (Lepidoptera: Pyralidae) and suppress its immune reactions to ensure the egg survival. The present study demonstrates that another female-injected factor calyx fluid extracted from the P. turionellae ovary is also responsible for the suppression of G. mellonella immunity. The total hemocyte counts of G. mellonella decrease after treatment with calyx fluid in a concentration-dependent manner. Significant reductions in cell viability are also observed at all calyx fluid doses both in vivo and in vitro. The analyses of the beads injected into the insects as encapsulation targets revealed that the number of encapsulated beads reduced significantly compared to controls post-calyx fluid injection. The injection of the highest calyx fluid dose (1 female equivalent calyx) is sufficient to completely inhibit the strong encapsulation and melanization reactions of the last instar larvae 24 h post-injection. These results demonstrate that P. turionellae calyx fluid is required to regulate host immunity for successful parasitization.

Insects have an effective innate immune system that includes both cellular and humoral responses for defense against pathogens. Antimicrobial peptides like gallerimycin and galiomycin, as well as immune proteins like hemolin, are the important effectors of the humoral immune response in Galleria mellonella L. (Lepidoptera:Pyralidae). Encapsulation, on the contrary, is one of the important cellular immune responses. This study investigated the tissue‐specific expression of an immune effector in G. mellonella larvae after injection with Candida albicans (C.P. Robin) (Ascomycota: Debaryomycetaceae) and silica beads. The gene expression of gallerimycin, galiomycin, and hemolin was examined in total larvae, hemocytes, and fat bodies at 4 and 24 h following injection. Our findings indicate that hemocytes serve as the main site for AMP synthesis, especially after bead injection, implying a more effective immune recognition mechanism relative to pathogen injection. Furthermore, we detected higher hemolin expression in hemocytes than fat tissue, indicating its role in hemocyte‐mediated immune responses. Encapsulation rates were also evaluated in bead‐injected larvae. At 4 h post‐injection, most beads were weakly encapsulated, whereas by 24 h, the majority were strongly encapsulated, reflecting a time‐dependent maturation of the immune response. These results show that G. mellonella has a unique immune system, with hemocytes playing a key role in regulating AMP production and immune responses during infection. This study provides deeper insights into the molecular and cellular mechanisms of insect immunity, positioning G. mellonella as a valuable model for studying host–pathogen interactions.