Increased caspase-3 immunoexpression and morphology alterations in oenocytes and trophocytes of Apis mellifera larvae induced by toxic secretion of Epormenis cestri

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 la...

ver descrição completa

Detalhes bibliográficos
Autores: Viotti, María H, Juri, Pablo, Lombide, Paula, Presentado, María L., Verdes, José Manuel, Nogueira, Enrique, Invernizzi Castillo, Ciro, Pedrana, Graciela
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2021
País:Uruguay
Recursos:Universidad de la República
Repositório:COLIBRI
Idioma:inglês
OAI Identifier:oai:colibri.udelar.edu.uy:20.500.12008/39032
Acesso em linha:https://hdl.handle.net/20.500.12008/39032
Access Level:Acceso aberto
Palavra-chave:Caspase-3
Honeybee larvae
Oenocytes
Trophocytes
River disease
Descrição
Resumo: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-day-old 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.