Abstract
Vitellogenesis and oocyte maturation require anautogenous female Anopheles mosquitoes to obtain a bloodmeal from a vertebrate host. The bloodmeal is rich in proteins that are readily broken down into amino acids in the midgut lumen and absorbed by the midgut epithelial cells where they are converted into lipids and then transported to other tissues including ovaries. The stearoyl-CoA desaturase (SCD) plays a pivotal role in this process by converting saturated (SFAs) to unsaturated (UFAs) fatty acids; the latter being essential for maintaining cell membrane fluidity amongst other housekeeping functions. Here, we report the functional and phenotypic characterization of SCD1 in the malaria vector mosquito Anopheles coluzzii. We show that RNA interference (RNAi) silencing of SCD1 and administration of sterculic acid (SA), a small molecule inhibitor of SCD1, significantly impact on the survival and reproduction of female mosquitoes following blood feeding. Microscopic observations reveal that the mosquito thorax is quickly filled with blood, a phenomenon likely caused by the collapse of midgut epithelial cell membranes, and that epithelial cells are depleted of lipid droplets and oocytes fail to mature. Transcriptional profiling shows that genes involved in protein, lipid and carbohydrate metabolism and immunity-related genes are the most affected by SCD1 knock down (KD) in blood-fed mosquitoes. Metabolic profiling reveals that these mosquitoes exhibit increased amounts of saturated fatty acids and TCA cycle intermediates, highlighting the biochemical framework by which the SCD1 KD phenotype manifests as a result of a detrimental metabolic syndrome. Accumulation of SFAs is also the likely cause of the potent immune response observed in the absence of infection, which resembles an auto-inflammatory condition. These data provide insights into mosquito bloodmeal metabolism and lipid homeostasis and could inform efforts to develop novel interventions against mosquito-borne diseases.
Highlights
In preparation for reproduction, anautogenous female mosquitoes must ingest vertebrate blood to improve their energy status and to stimulate vitellogenesis
Stearoyl-CoA desaturase is a rate limiting key enzyme regulating the ratio of SFAs to UFAs that is essential in the maintenance of cell membrane fluidity, proliferation, lipid accumulation and signaling
We demonstrate that loss-of-function of SCD1 in adult female A. coluzzii mosquitoes, the main vector of human malaria in West and Central sub-Saharan Africa, leads, upon blood feeding, to a highly skewed SFA:UFA ratio, loss of cell membrane integrity, transcriptional and metabolic reprogramming and various other detrimental physiological effects, including an acute auto-inflammatory condition and compromised reproduction
Summary
In preparation for reproduction, anautogenous female mosquitoes must ingest vertebrate blood to improve their energy status and to stimulate vitellogenesis. This induces massive mobilization of lipids from the fat body to the ovaries where they serve as the principal energy source for the maturing oocytes and the developing embryos [1,2,3]. Lp caries DAGs from the midgut directly to the ovarian tissues where they convert into TAGs [5] In addition to their importance as energy resource, lipids are crucial for signal transduction and maintenance of membrane fluidity of the midgut cells [6,7]
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