Making a meal of it: Mosquito spit protein controls blood feeding

Other salivary proteins have more specific roles antagonizing the host's immune system. Thus, sand fly saliva causes the death of host defensive white blood cells, while a salivary protein of the mosquito vector of dengue and Zika virus modifies the host immune response to be more anti-inflammatory rather than lethal to malarial protozoans.

Previous work identified a salivary protein (AAPP) of a mosquito vector of human malaria that blocks the binding of platelets to collagen, thus inhibiting clot formation after biting. Now, an international team led by Kanazawa University has investigated the function of AAPP in mosquito blood feeding.

In work reported in Scientific Reports, the team modified a transgene expression system to specifically express an artificial antibody against AAPP under the control of the AAPP promoter in the salivary glands of mosquitoes. They first confirmed that the antibody prevented AAPP binding to collagen in transgenic mosquitoes by forming a complex with AAPP protein. They then turned their attention to the effects of this inhibition.

"We studied the behavior of transgenic mosquitoes expressing the anti-AAPP antibody compared with wild-type controls when feeding on mouse hosts," says first author Ashekul Islam. "Transgenic mosquitoes took significantly longer to establish feeding after inserting their mouth parts into the host (probing time), and also had significantly prolonged prediuresis times."

Prediuresis is the process by which blood-sucking insects excrete drops of fluid to concentrate ingested blood protein within a small volume that fits in their midgut. However, long probing and prediuresis times come at a risk because they alert hosts to the action of biting, which can be detrimental to the insect. Transgenic mosquitoes also performed worse than their wild-type counterparts in terms of the volume of blood ingested, which directly reduced their egg production.

"Despite these clear behavioral changes, there was no difference in the number of malarial parasite oocysts developing within wild-type or transgenic mosquitoes," says corresponding author Shigeto Yoshida. "This shows that the size of the blood meal alone did not affect parasite development in our laboratory model."

In the real world, however, the authors believe that the high fitness demands of their parasite burden would push transgenic mosquitoes with inactivated AAPP over the edge.