Abstract
There remains an urgent need for knowledge regarding the molecular and genetic mechanisms in Aedes aegypti to support the fight against mosquito-borne illness, one of these areas being xenobiotic transport. If xenobiotic transport is disrupted, the accumulation of foreign molecules can reach toxic levels, leading to mortality. Therefore, transport by transmembrane proteins is an important consideration in the processes that govern mosquito metabolism and survival. We have identified six genes we speculate to be novel organic cation transporters (OCTNs) or organic cation transporters (OCTs) in Ae. aegypti. To measure the potential function of these transporters, female Ae. aegypti were injected with a blood meal size bolus of saline containing the xenobiotics Alizarin Yellow GG, Alizarin Yellow R, and Olsalazine and then clearance was quantified. mRNA expressions were analyzed 2 h and 24 h post injections in relation to xenobiotic exposure. Our findings demonstrate that xenobiotics had limited effect on the putative transporter expression profiles, but the molecular structure of the xenobiotics dramatically modified the volume and composition of the excreted materials, as well as changing the mortality. Overall, the mechanisms and key players underlying Ae. aegypti xenobiotic transport remain largely uncharacterized, but the results of this study are an important step in expanding knowledge of OCT(N)s in mosquitoes and understanding mosquito physiology. Targeting these proteins may offer new avenues for mosquito control.