For more than 60 years, sporadic cases of massive summer honey bee larvae mortality in colonies located near freshwater systems with abundant riparian vegetation have been reported in Uruguay. This odd phenomenon, known as “River disease” by beekeepers, can lead to colony death by depopulation. The aim of this study was to detect the causes of larvae death. Different experiments and analyses were performed using affected apiaries located between two important water courses. 1 day old larvae were the most susceptible and substances that killed the larvae were present in the nectar but not in the pollen. A palynological analysis of nectar samples showed that bees collect this resource from commonly pollinated floral species in the country. However, abundant fungi spores and conidia were found, which indicates that the bees also collected honeydews. In the riparian vegetation, bees were observed collecting the secretions of the planthopper Epormenis cestri on Sebastiania schottiana trees. It was found that the mortality period of larvae overlaps with the presence of E. cestri. Larvae maintained in the laboratory were fed (i) nectar from healthy colonies, (ii) nectar from affected colonies, and (iii) secretions of E. cestri. The mortality of the larvae that received nectar from colonies affected with River disease and secretions of E. cestri was higher than the mortality of those receiving nectar from healthy colonies. This represents the first report of planthopper honeydew causing mass larval mortality in honey bees.
Toxic honeydew produced by Flatidae Epormenis cestri in Uruguay has been shown to cause among honeybees (Apis mellifera) colonies a massive larva death called “River disease”, but the intrinsic mechanisms are still unknown. Because fat body cells, oenocytes and trophocytes, are known to regulated larvae metabolism, and to be affected by xenobiotics, we tested whether apoptosis of these cells can be an underlying cause of larvae death. Ten colonies were divided into two groups and fed with common honey or toxic honeydew obtained from colonies affected by “River disease”. Five-dayold larvae were collected and processed for histology and immunohistochemistry for caspase-3. The area, diameter, and immunostaining area in oenocytes and trophocytes were measured. The oenocyte and trophocyte cellular area decreased in the treated group (p=0.002; p<0.001 respectively) compared to the control group. The diameter of oenocytes (p=0.0002) and trophocytes (p<0.0001) decreased in the treated group. Caspase-3 was detected in cytoplasm in the control group but in the cytoplasm and nucleus in the treated group. The caspase-3 immunostaining area increased in oenocytes (p<0.002) and trophocytes (p<0.0001) of the treated group. The ingestion of toxic honeydew altered the morphology, localization and immunoexpression of caspase-3 in fat body cells, which suggests that the deregulation of the apoptotic mechanism affected the normal development in A. mellifera larvae.
agencias argentina y brasilera. La lógica de calidad del sistema de acreditación de Brasil pone énfasis en la formación del plantel docente y Argentina pone énfasis en los procesos de enseñanza y de aprendizaje. La carrera acreditaría con los parámetros argentinos pero debe mejorar aspectos de la formación académica de sus docentes para lograr acreditar en Brasil. Este trabajo permitió ajustar el Plan de Desarrollo de la Facultad de Veterinaria.
In Uruguay, the excretions of the flatidae Epormenis cestri when located in sarandí colorado trees (Sebastiania schottiana) are the cause of the massive death of young honeybee larvae, a phenomenon that beekeepers call River disease. A strong income of honeydew is frequently observed in these affected colonies despite the continuous loss of bees due to lack of replacement. The aim of this study was to determine a handling of the colonies that allows obtaining honeydew honey. Forty-eight colonies were transported to an apiary affected by River disease and were divided into 5 groups according to the following treatments: Group 1: regular honeydew harvest, adding of brood and sugar syrup supply (N=10); Group 2: regular honeydew harvest and sugar syrup supply (N=10); Group 3: regular honeydew harvest and adding of brood (N=10); Group 4: regular honeydew harvest (N=10); Group 5: only one harvest of honeydew once the study had finished (N=8). The colonies from groups 1 and 3 produced the biggest amount of honeydew honey, averaging 32.0 and 28.6kg, respectively. The physicochemical analysis of honeydew honey showed characteristics of this product such as high electrical conductivity (0.98-1.14 mS/cm), diastase activity (>50%) and color (71-83 mm Pfund). This study provides the basis of a colony handling that allows beekeepers to obtain important harvests of a honeydew honey not yet known in the international market.
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