This research uncovers the role of iron homeostasis in mosquito fertility and Plasmodium transmission, indicating a new malaria control strategy.
Iron metabolism is essential for both mosquito reproductive fitness and Plasmodium development within the mosquito, yet this axis has remained insufficiently explored as a potential target for malaria control. Ferritin, the major iron-storage protein and a central regulator of iron homeostasis, has not been biochemically or functionally characterized in any hematophagous insect to date. Our computational and phylogenetic analyses reveal that mosquito ferritin represents a unique case, exhibiting a chimeric architecture that combines conserved iron-binding motifs with distinctive heme-coordinating residues, resulting in an exceptionally high heme-binding affinity that surpasses that of bacterioferritin. Functional knockdown of the ferritin heavy-chain subunit in adult Anopheles stephensi females caused profound defects in reproductive tissue development, confirming its essential role in mosquito physiology, iron storage, and transport. Furthermore, capitalizing on the host-parasite competition for iron, we screened multiple chelators and identified β-thujaplicin as a potent transmission-blocking agent that significantly suppressed Plasmodium oocyst development. Together, these findings establish mosquito ferritin as an evolutionarily distinct, physiologically essential protein and position iron homeostasis as a powerful dual-target axis for next-generation transmission-blocking interventions.
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Tupe et al. (2026) studied this question.
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