Expression and Activity of Lysozyme in Apis Mellifera Carnica Brood Infested with Varroa Destructor

Varroa destructor is a parasitic mite that attacks the honey bee, and previous studies have suggested that parasitosis caused by this mite is accompanied by immunosuppresion in the host. In this study, the effect of mite infestation on the expression of the lysozyme-1 (lys-1) gene and lysozyme activity in Apis mellifera carnica was determined. The experiment was carried out on the five developmental stages of honey bee workers and drones. Developmental and gender-related differences in gene expression and lysozyme activity were observed in a Varroa destructor-infested brood. The relative expression of the lys-1 gene increased in a infested worker brood and decreased in a drone brood except for P3 pupae. In the final stage of development, the lys-1 gene expression was significantly lower in infested newly emerged workers and drones. Changes in the relative expression of the lys-1 gene in infested individuals was poorly manifested at the level of enzyme activity, whereas at the two final stages of development (P5 and I) there was a positive correlation between relative lys-1 expression and lysozyme activity in infested bees of both genders (r=0.988, r=0.999, respectively). The results of this study indicate that V. destructor influences the lysozyme-linked immune response in bees

Expression of the Prophenoloxidase Gene and Phenoloxidase Activity, During the Development of Apis Mellifera Brood Infected with Varroa Destructor

The pathogenesis of varroasis has not been fully explained despite intensive research. Earlier studies suggested that parasitic infections caused by Varroa destructor mites were accompanied by immunosuppression in the host organism. The objective of this study was to analyse the influence of varroasis on one of the immune pathway in Apis mellifera measured by the expression of the prophenoloxidase (proPO) gene and the enzymatic activity of this gene’s product, phenoloxidase (EC 1.14.18.1). An evaluation was done of five developmental stages of honey bee workers and drones. The relative expression of proPO decreased in infected individuals. The only exceptions were worker prepupae (PP) and drone pupae with brown eyes and dark brown thorax (P5) where propo gene expression was 1.8-fold and 1.5-fold higher, respectively, than in the control. Phenoloxidase (PO) activity was 2.8-fold higher in infected pp workers and 2-fold higher in p5 drones in comparison with uninfected bees. Phenoloxidase activity was reduced in the remaining developmental stages of infected workers and drones. The relative expression of proPO was positively correlated with the relative PO activity in both workers (r = 0.988) and drones (r = 0.996). The results of the study indicate that V. destructor significantly influences the phenoloxidase-dependent immune pathway in honey bees

The Proteolytic Activity of Diapausing and Newly Hatched Red Mason Bees (Osmia Rufa: Megachilidae)

Osmia rufa is a solitary bee that is used commercially for pollinating crops. The bee enters obligatory diapause as an imago. The activity of proteolytic enzymes during diapause has not been investigated. We studied the proteinase activity on four substrates - casein, haemoglobin, bovine serum albumin (BSA ), and gelatine - during diapause (from October to March) and in newly hatched males and females in April. During diapause, greater fluctuations in enzyme activity levels were noted in males than in females, and a significant decrease in male enzyme activity was observed in January and March. Male enzymes were most effective in decomposing gelatine; whereas, female enzymes were equally effective in hydrolysing gelatine and BSA . The differences in substrate preferences between male and female enzymes were particularly pronounced in October and in the newly hatched individuals. The levels of gelatinolytic activity likely indicate that a high proportion of proteinases in O. rufa are elastase-like enzymes. They are involved in the digestion and remodelling of proteins with numerous peptide bonds formed by amino acids with short side-chains