The sand fly Phlebotomus papatasi Scopoli, 1786, the vector of Leishmania major Yakimoff et Schokhor, 1914, is found in desert areas where sugars are scarce but also in habitats that abound in sugar sources. The sand flies require sugar meals from plant sources for their energy requirements and to hydrolyze these complex sugars, they need a repertoire of glycosidases. We presumed that there are differences in the levels of glycosidase activities in flies from such habitats and also assumed that they may be instrumental in modulating the flies' susceptibility to L. major infections. Phlebotomus papatasi originating from diverse ecological habitats ranging from an oasis to desert sites were colonized. They were analyzed for weight changes and glycosidase activities before and after feeding on 1M sucrose solution. Oasis flies were smaller than desert flies but took larger sugar meals. Homogenates of these flies hydrolyzed 16 synthetic and 2 natural glycoside substrates to varying degrees. The arid-region flies tended to produce more glycosidase activity than those originating in sugar-rich environments, especially sucrase, α- and β-glucosidase, α-fucosidase, α-mannosidase, and α- and β-N-acetylgalactosaminidase. However, chitinolytic enzyme activities and particularly the β-N-acetylhexosaminidase activity of oasis flies were higher than other flies tested. In comparing the desert flies, there were also significant differences in glycolytic enzyme activities between the spring-line (flowering season) of flies and the autumn-line (end of dry season) flies. A range of saccharide inhibitors was tested to demonstrate the specificity of the enzymes.
Sandfly females, while feeding on the host, excrete urine to concentrate proteins of the bloodmeal and restore weight and water balance. This process, analogous to prediuresis in mosquitoes, was observed in 100% of Phlebotomus papatasi (Scopoli) and 85% of P. duboscqi Neveu-Lemaire females studied. Individual females, however, differed in duration of prediuresis and in the number of ejected urine droplets. In both species the prediuresis generally started 1-2 min after the commencement of feeding and the variation in urine production was positively correlated with the length of feeding. The first one or two droplets were opaque whitish while the remaining ones were clear. Erythrocytes were found sporadically in first droplets of some females. Representative prediuresis in P. duboscqi included 27 droplets, i.e., about 325 nl urine in total, ejected during 8 min of feeding. The study revealed prediuresis in P. papatasi and P. duboscqi as a regular physiological process which may have consequences in transmission of infective diseases.