The Salivary Secretome of the Tsetse Fly Glossina pallidipes (Diptera: Glossinidae) Infected by Salivary Gland Hypertrophy Virus

Tsetse fly (Diptera; Glossinidae) transmits two devastating diseases to farmers (human African Trypanosomiasis; HAT) and their livestock (Animal African Trypanosomiasis; AAT) in 37 sub-Saharan African countries. During the rainy seasons, vast areas of fertile, arable land remain uncultivated as farmers flee their homes due to the presence of tsetse. Available drugs against trypanosomiasis are ineffective and difficult to administer. Control of the tsetse vector by Sterile Insect Technique (SIT) has been effective. This method involves repeated release of sterilized males into wild tsetse populations, which compete with wild type males for females. Upon mating, there is no offspring, leading to reduction in tsetse populations and thus relief from trypanosomiasis. The SIT method requires large-scale tsetse rearing to produce sterile males. However, tsetse colony productivity is hampered by infections with the salivary gland hypertrophy virus, which is transmitted via saliva as flies take blood meals during membrane feeding and often leads to colony collapse. Here, we investigated the salivary gland secretome proteins of virus-infected tsetse to broaden our understanding of virus infection, transmission and pathology. By this approach, we obtain insight in tsetse-hytrosavirus interactions and identified potential candidate proteins as targets for developing biotechnological strategies to control viral infections in tsetse colonies

Square Wave Voltammetry in the Determination of Ni2+ and Al3+ in Biological Samples

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)In this contribution, the amounts of Ni (nickel) and Al (aluminum) in tilapias (Oreochromis niloticus) were determined using square wave voltammetry (SWV) with glassy carbon working microelectrode with a mercury thin film, platinum counter electrode, and Ag/AgCl reference electrode. Ni was studied through the formation of the dimethylglyoxime-Ni (Ni-DMG) complex, while Al was studied through the formation of the Alizarin R-Al complex. The detection limit found for Ni-DMG and Alizarin R-Al complexes were 1.70 x 10(-7) and 1.0 x 10(-8) mol L-1, respectively. The voltammetric anodic curves for the Alizarin R-Al complex were recorded over the potential range from -0.8 to -0.05 V while the voltammetric cathodic curve for the Ni-DMG complex was recorded over the potential range from -0.7 to -1.2 V. These methods detected low concentrations of Ni and Al in biological samples efficiently.241114431447Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES