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Malaria is a tropical disease that takes a huge toll on lives as well as causes massive economic loss is one of the four deadliest
vector-borne diseases caused by the obnoxious mosquitoes. Insecticide resistance and lack of effective vaccines have
led to alternative strategies to control this disease. Blocking the Plasmodium in the Anopheles itself i.e., transmission-blocking
can prove to be an effective approach. Studies reveal that insect peroxidases are involved in detoxification, stabilization of
extracellular matrices, development and the immunity. Our study focuses on the immunobiology of Anopheles stephensi, the
Indian urban malaria vector. Heme peroxidases, a large group of immune proteins are involved in regulation of major immune
pathways. We have characterized DBLOX-double peroxidase, a mysterious Anopheles stephensi heme peroxidase which contains
two peroxidase domains which apparently are a result of domain duplication. Sequencing of the two domains followed by
expression analysis of immune challenged mosquitoes with pathogens reveals that this gene is probably getting modulated by
the pathogens. Also, it shows a heightened expression in the pupa stage of the mosquito development indicating its probable
role in pupa-adult metamorphosis. The in silico prediction analysis N- terminal signal peptide, conserved motifs (active site,
heme binding site), protein modeling etc., have also been carried out implicating it to be a secreted protein. We hypothesize
that this gene might have some crucial role to play in the mosquito innate immunity and further gene silencing analysis can
clear its probable role in immunity. Hence, it can prove as an effective candidate for transmission-blocking strategies.