Feeding Apis mellifera Larvae With Saccharomyces cerevisiae From The Brewing Industry Improves Their Resistance To Paenibacillus larvae And Their Primary Antioxidant Enzymatic Activity

MOLINÉ, M. P.; MORAN GIARDINI, P.; DOMINGUEZ, E.; QUINTANA, S.; VAZQUEZ, M.M.; D´ARCANGELO, V.; FERNÁNDEZ, N.; DAMIANI, N.; GENDE, L.

Congreso; 3th International Congress on Bee Science; 2024

The spore-producing bacterium, Paenibacillus larvae, causes American foulbrood (AFB) in the brood of Apis mellifera bees and has been associated with their oxidative stress. It ranks among the deadliest bacterial pathogens that affect bee colonies. It has been observed that using beneficial microorganisms as a nutritional supplement can mitigate the impacts of stress by enhancing the immune and antioxidant systems of individuals. In recent years, Argentina has increased the production of craft beer, which generates a large amount of residual Saccharomyces cerevisiae yeast. The most commonly used yeasts in the production of ALE beer are S05. The aim of this study was to evaluate the effect of supplementing bee larvae with S. cerevisiae and compare its effect between healthy larvae and those inoculated with P. larvae spores in terms of infection and antioxidant capacity. For this, groups of larvae were fed with four different diets: control (Yeast Extract, Glucose, Fructose, Royal Jelly and Water), SD (control with 105 cells/ml of yeast), ID (control with the median lethal dose of P. larvae) and SDI (control plus 105 cells/ml of yeast and the median lethal dose of P. larvae).The larvae supplemented with yeast showed improved survival compared to the controls. The increasing was from 5.01 to 5.46 days for P. larvae inoculated larvae fed without and with S05, respectively. Furthermore, the activity of the primary antioxidant enzymes catalase (CAT) and superoxide dismutase (SOD) was estimated in larvae of each group and expressed as units per μg of total protein. Larvae of SD group showed an augment in CAT and SOD activity compared to larvae fed with control diet (CAT= from 1.63±0.97 to 1.78±0.99 not-statistically significant; SOD= from 0.26±0.11 to 0.40±0.17 statistically significant). In the cases of ID and SDI groups, CAT activity of SDI (3.06±2.22) increased statistically significant respect to larvae of ID (1.56±1.16) and SOD activity remained without changes (from 0.21±0.17 for SDI to 0.21±0.20 for ID). Our results demonstrate that feeding larvae with S. cerevisiae yeast, a by-product from the brewing industry, can increase larval resistance to AFB pathology by enhancing their oxidative state, thereby contributing to the circular economy.