Vector-borne diseases and especially malaria are responsible for more than half million deaths annually. The increase of insecticide resistance in wild populations of
Anopheles
malaria vectors emphasises the need for novel vector control strategies as well as for identifying novel vector targets. Venus kinase receptors (VKRs) constitute a Receptor Tyrosine Kinase (RTK) family only found in invertebrates. In this study we functionally characterized
Anopheles
VKR in the Gambiae complex member,
Anopheles
coluzzii
. Results showed that
Anopheles
VKR can be activated by L-amino acids, with L-arginine as the most potent agonist. VKR was not required for the fecundity of
A. coluzzii
, in contrast to reports from other insects, but VKR function is required in both
Anopheles
males and females for development of larval progeny.
Anopheles
VKR function is also required for protection against infection by
Plasmodium
parasites, thus identifying a novel linkage between reproduction and immunity in
Anopheles
. The insect specificity of VKRs as well as the essential function for reproduction and immunity suggest that
Anopheles
VKR could be a potentially druggable target for novel vector control strategies.
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